1. Developmental Biology

A Tgfbr1/Snai1-dependent developmental module at the core of vertebrate axial elongation

  1. André Dias
  2. Anastasiia Lozovska
  3. Filip J Wymeersch
  4. Ana Nóvoa
  5. Anahi Binagui-Casas
  6. Daniel Sobral
  7. Gabriel G Martins
  8. Valerie Wilson
  9. Moises Mallo  Is a corresponding author
  1. Instituto Gulbenkian de Ciência, Portugal
  2. Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, United Kingdom
  3. Faculdade de Ciências da Universidade de Lisboa, Portugal
https://doi.org/10.7554/eLife.56615
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Cite this article
  1. André Dias
  2. Anastasiia Lozovska
  3. Filip J Wymeersch
  4. Ana Nóvoa
  5. Anahi Binagui-Casas
  6. Daniel Sobral
  7. Gabriel G Martins
  8. Valerie Wilson
  9. Moises Mallo
(2020)
A Tgfbr1/Snai1-dependent developmental module at the core of vertebrate axial elongation
eLife 9:e56615.
https://doi.org/10.7554/eLife.56615
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Abstract

Formation of the vertebrate postcranial body axis follows two sequential but distinct phases. The first phase generates pre-sacral structures (the so-called primary body) through the activity of the primitive streak on axial progenitors within the epiblast. The embryo then switches to generate the secondary body (post-sacral structures), which depends on axial progenitors in the tail bud. Here we show that the mammalian tail bud is generated through an independent functional developmental module, concurrent but functionally different from that generating the primary body. This module is triggered by convergent Tgfbr1 and Snai1 activities that promote an incomplete epithelial to mesenchymal transition on a subset of epiblast axial progenitors. This EMT is functionally different from that coordinated by the primitive streak, as it does not lead to mesodermal differentiation but brings axial progenitors into a transitory state, keeping their progenitor activity to drive further axial body extension.

Introduction

Formation of the vertebrate body is a complex and dynamic process involving a series of sequential growth and patterning activities. In amniotes, the primordia of the different organs and body structures are laid down progressively in a head to tail sequence by dedicated axial progenitors with stem cell-like properties (Stern et al., 2006). Although continuous, this process can be divided into distinct steps based on structural and regulatory features. At the end of gastrulation, during the so-called primary body formation (i.e. post-occipital region of the head, neck and trunk) axial progenitors are located in the epiblast, an epithelial layer at the caudal embryonic end, and their activity is organized by the primitive streak (PS) (Aires et al., 2018; Holmdahl, 1925; Steventon and Martinez Arias, 2017). At this stage, the embryo contains axial progenitors with different potencies. These include the neuro-mesodermal progenitors (NMPs), a bipotent cell population that can generate both neural and mesodermal tissues, and the lateral and paraxial mesoderm progenitors (LPMPs), with potential limited to mesodermal lineages, that together with the endoderm generate organic systems involved in most vital and reproductive functions (Wilson et al., 2009; Wymeersch et al., 2016). After PS regression and caudal neuropore closure, the embryo engages in secondary body formation (essentially the tail). At this stage, axial progenitors, which are now restricted to NMPs, are located in the tail bud (Bénazéraf and Pourquié, 2013; Henrique et al., 2015; Steventon and Martinez Arias, 2017; Wilson et al., 2009).

A large number of genetic experiments led to the identification of factors regulating axial progenitor activity. Some of these factors, including Wnt3a, Fgf8, T(Brachyury) or the Cdx gene family, are required during both primary and secondary body axis formation, as their partial or total inactivation produce different degrees of axial truncations depending on the levels of gene activity left available to the axial progenitors (Boulet and Capecchi, 2012; Greco et al., 1996; Herrmann et al., 1990; Naiche et al., 2011; Savory et al., 2011; Takada et al., 1994). Other factors show regional specific activity, determining whether progenitors generate trunk or tail structures (Aires et al., 2019; Aires et al., 2018; Aires et al., 2016; DeVeale et al., 2013; Robinton et al., 2019; Wymeersch et al., 2019). Gain and loss of function experiments in the mouse revealed a central role for Pou5f1 (also known as Oct4) in trunk development. Indeed, conditional Pou5f1 inactivation after it had fulfilled its role during preimplantation and early post-implantation stages resulted in embryos lacking trunk structures but still containing recognizable tails (DeVeale et al., 2013). Conversely, sustained transgenic Pou5f1 expression in the axial progenitor region extended trunk development at the expense of the tail (Aires et al., 2016). Pou5f1 importance for vertebrate trunk development was further revealed by the finding that the remarkably long trunks characteristic of the snake body plan seemed to derive from a chromosomal rearrangement involving the Pou5f1 locus during vertebrate evolution that placed this gene under the control of regulatory elements that maintained its expression for very long developmental periods (Aires et al., 2016).

In the tail bud, axial progenitor activity is independent of Pou5f1 (DeVeale et al., 2013). Genetic experiments in mouse embryos revealed that in this area the Lin28/let-7 axis together with Hox13 genes, particularly those belonging to the HoxB and HoxC clusters, occupy a prevalent position in the regulatory hierarchy of axial progenitors in the tail bud (Aires et al., 2019; Robinton et al., 2019). Interestingly, while tail bud progenitors show drastic responses to variations in the Lin28/let-7 pathway and are strongly inhibited by premature activation of Hox13 genes, their trunk counterparts are largely non-responsive to those activities (Aires et al., 2019; Robinton et al., 2019), suggesting the existence of differences in cell competence, at the progenitor level, during primary and secondary body formation. The differences in progenitor regulation at trunk and tail levels seem to be also associated with changes in their functional characteristics. For instance, while NMPs produce neural tube at both axial levels, they are thought to follow different mechanisms in the two regions (Catala et al., 1995; Schoenwolf, 1984; Schoenwolf and Smith, 1990). Differences can also be observed in the properties of their mesodermal derivatives. In particular, while disconnecting the Lfng cycling activity disturbs somitogenesis at trunk levels, it has no or minor effects in the tail (Shifley et al., 2008; Williams et al., 2014). Conversely, forced Hoxb6 expression blocks tail somitogenesis but has no effect at trunk levels (Casaca et al., 2016).

Despite these major differences in axial progenitor regulation and competence, lineage tracing experiments indicate that post-occipital neural and mesodermal structures are generated from a progenitor pool that is, at least to some extent, maintained along the main vertebrate body axis (Tzouanacou et al., 2009), thus implying that transition from primary to secondary body development entails unknown molecular mechanisms occurring at the progenitor level (Aires et al., 2018). We have previously shown that Gdf11 activity plays a relevant role in this process (Aires et al., 2019; Jurberg et al., 2013). However, partial redundancy by Gdf8 (McPherron et al., 2009) complicates proper evaluation of this process, as trunk-to-tail transition eventually becomes activated in Gdf11 mutant embryos, although at more caudal axial levels and generating a number of abnormal structures (Aires et al., 2016; McPherron et al., 1999). Therefore, to evaluate the underlying molecular mechanisms, we compared the molecular characteristics of axial progenitors at progressively later developmental stages using a single-cell RNA-sequencing (scRNA-seq) approach and found that the switch from primary to secondary body development entails an incomplete epithelial to mesenchymal transition (EMT) affecting a subset of axial progenitors in the epiblast. Further analyses showed that this process is functionally different from that generating primary body structures and that it is driven by the sequential activity of Tgfbr1 and Snai1. Together, our data uncovered a distinct functional developmental module generating the tail bud from a subset of epiblast axial progenitors, that initiates secondary body formation in mouse embryos.

Results

Axial progenitors undergo an incomplete EMT during axial extension

To evaluate the underlying mechanisms of the changes in progenitor activity as they switch from generating primary to secondary body structures, we compared their molecular characteristics at progressively later developmental stages using a scRNA-seq approach. We first obtained scRNA-seq data from the caudal lateral epiblast (CLE) of early head fold mouse embryos [~embryonic stage (E) 8.0], which contain axial progenitors (Cambray and Wilson, 2002; Tam and Behringer, 1997; Figure 1A). The dissected tissue included some nascent mesoderm, but these cells segregated from those of the epiblast using the single-cell consensus clustering (SC3) framework (Kiselev et al., 2017), producing two well-defined clusters (Figure 1A and Figure 1—figure supplement 1A). We then compared these data with published scRNA-seq data from CLE regions of E8.5 and E9.5 embryos (Gouti et al., 2017), which similarly to the E8.0 single-cells, contained some nascent mesoderm. Principal component analysis (PCA) of all these single-cell transcriptomes indicated that the epiblast cluster from E8.0 embryos becomes more similar to the mesodermal component (Figure 1A; Figure 1—figure supplement 1B,C). Interestingly, differential gene expression analysis revealed an increase of mesenchyme-associated genes and a concomitant decrease of some epithelial markers (Kalluri and Weinberg, 2009; Lamouille et al., 2014) in epiblast clusters as development proceeds (Figure 1B). For instance, we observed a transition from Cdh1 (E-cadherin) to Cdh2 (N-cadherin), as well as downregulation of Epcam and up-regulation of Vim. This tendency was also observed in cells co-expressing Sox2 and T (Figure 2), typically associated with NMPs (Cambray and Wilson, 2007; Koch et al., 2017; Martin and Kimelman, 2012; Olivera-Martinez et al., 2012; Tsakiridis et al., 2014; Wymeersch et al., 2016). These results suggest that progress into tail bud stages requires that axial progenitors undergo an EMT.

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Axial progenitors undergo an incomplete EMT during axial extension.

(A) PCA analysis of CLE scRNA-seq datasets from E8.0, E8.5 and E9.5 embryos. Dimension one represents developmental time, whereas dimension two shows differences in cell characteristics. Epiblast and mesodermal clusters are indicated. During primary body formation, epiblast clusters converge towards the mesodermal compartment. (B) Z-score heatmap gene expression analysis of selected genes and marker genes (highlighted in bold), obtained with the SC3 when pre-clustered E8.0 and E9.5 epiblast single-cells are forced to form two clusters. Downregulation of some epithelial-associated genes (e.g. Cdh1 and Epcam) together with upregulation of several mesenchymal-related genes (e.g. Cdh2, Vim, Zeb1) at E9.5 is observed. P-values are shown in Figure 1—source data 1. (C) Diagrams showing the regions used for the analysis in D and E. (D) Comparative heatmap representation of microarray gene expression between E8.5 node-streak border (NSB) and E10.5 chordoneural hinge (CNH). Epithelial and mesenchymal markers are indicated. (E) Comparative heatmap representation of RNA-seq gene expression in tail bud axial progenitors and a similar-staged reference total tail bud. Both (D and E) analysis indicated that loss of epithelial markers in tail bud axial progenitors is not complete (e.g. Tjp1 and Krt10). NT: Neural Tube; PM: Paraxial Mesoderm; LM: Lateral Mesoderm; GT: Gut; PS: Primitive Streak; * means Average.

Figure 1—source data 1

p-values corresponding to the SC3 analysis of RNA-seq values represented in Figure 1 and Figure 1—figure supplement 1.

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T and Sox2 double-positive cells acquire mesenchymal properties during primary body formation.

(A) RPKM (Reads per kilo base per million mapped reads) SPRING analysis of pre-clustered epiblast E8.0 and E9.5 single cells, organizes them in two clusters according to their developmental stage. T and Sox2 double-positive cells are shown circled in yellow. (B) Comparative gene expression analysis of epithelial (upper row) and mesenchymal (lower row) markers focused on T+ and Sox2+ epiblast cells suggest that they undergo an EMT between E8.0 and E9.5. The scRNA-seq values in RPKM used for this analysis are shown in Figure 2—source data 1.

Figure 2—source data 1

RPKM (Reads per kilo base per million mapped reads) values represented in Figure 2, Figure 2—figure supplement 1 and Figure 2—figure supplement 2.

https://cdn.elifesciences.org/articles/56615/elife-56615-fig2-data1-v1.xlsx

We further tested this idea in two additional ways. As the majority of axial progenitors in the Chordoneural Hinge (CNH; the region of the tail bud that drives tail elongation) are descended from cells in the Node-Streak Border (NSB) (Cambray and Wilson, 2007), we compared the transcriptome of these two regions of the mouse embryo using data from Wymeersch et al., 2019. This analysis revealed increased expression of mesenchymal-related genes (e.g. Snai1, Vim and Zeb1) and downregulation of some epithelial markers (e.g. Cdh1, Krt18 and Cldn4) in the CNH (Figure 1D). In a complementary approach, we examined the transcriptome of a cell population highly enriched in axial progenitors isolated from E10.5 tail buds (de Lemos et al., 2019), using as a reference the transcriptome of unsorted tail bud tissue (Aires et al., 2019). Again, many mesenchymal markers were highly expressed in the sorted axial progenitors, at levels comparable to those observed in the total tail bud (Figure 1E). Conversely, expression of many epithelial markers was significantly lower in the progenitor pool than in the reference tail bud. Therefore, the gene expression profile of tail bud axial progenitors is more consistent with a mesenchymal than with an epithelial phenotype, further suggesting that tail bud formation entails an EMT on the axial progenitors. Interestingly, however, in all our analyses the loss of epithelial characteristics in tail bud axial progenitors was not complete. Indeed, some epithelial markers maintained high expression levels (e.g. Tjp1, Lamb1) or were upregulated (e.g. Krt10 in the CNH) when axial progenitors moved into the tail bud (Figure 1D,E), thus indicating that the EMT involved in this process could be classified into the category of incomplete or transitional EMTs (further referred as tb-EMT), more akin to those described in metastatic processes than to those driving embryonic development (Kalluri and Weinberg, 2009; Lamouille et al., 2014; Nieto et al., 2016; Pastushenko et al., 2018). Interestingly, while during gastrulation axial progenitors undergoing EMT through the PS enter differentiation routes (e.g. mesoderm formation), tb-EMT keeps the progenitor properties of these cells, capacitating them to drive further axial extension from the tail bud (Aires et al., 2019; Rodrigo Albors et al., 2018; Tzouanacou et al., 2009). This further indicates that although gastrulation and tail bud formation both involve EMTs on axial progenitors within the epiblast, they seem to be functionally separate processes, suggesting that they should rely on different regulatory mechanisms.

Snai1 is required for axial progenitor mobilization to form the tail bud

Snail genes are among the most prominent EMT regulators in physiological and pathological processes (Barrallo-Gimeno and Nieto, 2005; Carver et al., 2001; Lomelí et al., 2009; Murray and Gridley, 2006; Nieto, 2002; Zeisberg and Neilson, 2009). From this gene family, Snai1 is a good candidate to be involved in EMT processes associated with axial extension, as in mouse embryos it is expressed in the PS region starting at early developmental stages (Hernández-Martínez et al., 2019; Nieto et al., 1992; Figure 2—figure supplement 1). Indeed, gene inactivation experiments in mouse indicated that Snai1 is involved in EMT processes during gastrulation (Carver et al., 2001). Interestingly, when this early Snai1 function was bypassed through a conditional approach that inactivated this gene in the epiblast using the Meox2-Cre driver (Murray and Gridley, 2006; Tallquist and Soriano, 2000) (hereafter termed Snai1-cKO), the embryos still failed to develop beyond ~E9.5 (a few embryos survive until E10.5) (Lomelí et al., 2009; Murray and Gridley, 2006), indicating an essential function of this gene after gastrulation.

Analysis of E9.5 Snai1-cKO embryos revealed a fairly well conserved development of trunk structures. In particular, these embryos had a well-defined neural tube, midgut, notochord and a considerable number of somites that, although smaller than those of wild type littermates, retained signs of anterior/posterior compartmentalization (Figure 3 and Figure 4Ae-j). The trunk identity of this part of the Snai1-cKO embryos was confirmed by the presence of characteristic intermediate and lateral mesoderm tissues, including forelimb buds, molecular signatures of urogenital system development (Figure 4Ak,l) and, in some rare embryos that developed until E10.5, hindlimb buds (Figure 4Ao,p). These observations indicate that formation of the primary body is fairly well conserved in Snai1-cKO embryos despite Snai1 being completely absent already at E8.0 (Murray and Gridley, 2006) when this region of the body is being laid down.

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Axial extension is disrupted, at the level of the trunk-to-tail transition, in the absence of Snai1.

(A) Wholemount in situ hybridization with the indicated probes in E9.5 wild type (WT) and Snai1-cKO embryos. Axial progenitor-related markers Fgf8, Nkx1-2, Cyp26a1 were abnormally restricted to the epithelium of the caudal protuberance of Snai1-cKO embryos (red arrows) and T and Wnt3a-stained embryos were substantially downregulated in the central component of the bulge mesenchyme. Tbx6 expression was observed in the epithelial-like component of the bulge (black arrowhead) in addition to its mesenchymal expression. Msgn1 was present in the presomitic mesoderm and in the mesenchymal component of the bulge. The white arrows in the Noto-stained embryos indicate the bifurcated or inverted notochord growth in the absence of Snai1. Sox2 was absent from the bulge region (white arrowhead) of Snai1-cKO embryos. Black arrows in the Foxa2 labelled embryos highlight the abnormal localization of hindgut endoderm in Snai1-cKO embryos. (B) 3D reconstructions of E9.5 Snai1-cKO and WT posterior/caudal structures: neural tube (green), open epiblast (light green), presomitic mesoderm (light blue), somites (dark blue), notochord (red) and endoderm (yellow). At this stage, the ectopic bulge of Snai1-cKO embryos forms a structure that resembles an abnormally extended open epiblast in which the closing neural plate fails to extend caudally. The notochord often bifurcates, with one end following the posterior gut endoderm that is detached from the rest of the embryonic structures (black arrow).

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Snai1-cKO embryos develop fairly-well organized primary body structures but are unable to form a tail bud.

(A) Wholemount in situ hybridization with the indicated markers in wild type (WT) and Snai1-cKO mutant embryos at E9.5 and E10.5. The insets show close ups of the caudal region. Transverse sections at the levels indicated in the whole-mount embryo are also shown. Cdx2 and Hoxc10 expression in Snai1-cKO embryos indicate that the bulge is the equivalent of the tail bud in similar stage wild type embryos. The black arrows in the Pax2-stained embryos indicate the presence of intermediate mesoderm in both Snai1-cKO and wild type embryos. At E9.5, Tbx18 expression and the combined in situ hybridization for Uncx4.1/Tbx4 and Uncx4.1/Pitx1, indicate the presence of fairly-well organized trunk somites and hindlimb buds (white arrowheads) in Snai1-cKO embryos, which is also highlighted in some mutant embryos, that survived at E10.5, with Tbx5 and Tbx4 expression. White arrows indicate that Sox2 is still downregulated in the bulge of E10.5 Snai1-cKO embryos, in comparison to the tail bud of wild type littermates. (B) 3D reconstructions of caudal structures of E10.5 wild type and Snai1-cKO embryos. Wild type embryos have a closed neural tube (in green), dorsal to the presomitic mesoderm (in blue) and somites (in dark blue). In contrast, Snai1-cKO embryos have a bifurcated notochord (red), detached endoderm (yellow) and the bulge resembles a still open caudal epiblast (in green). Somites are shown in dark blue and extra mesoderm in Snai1-cKO embryos is highlighted in cyan. Note that the structures posterior to the last somites in Snai1-cKO embryos did not extend further than at E9.5, leading to a shorter axis.

In contrast, the tail bud of E9.5 Snai1-cKO embryos was replaced by a protuberance protruding caudally from the trunk region of the embryo (Figure 3A,B, Figure 3—video 1, Figure 4Aa-j and Figure 4—video 1). The finding that in Snai1-cKO embryos Hoxc10 expression was restricted to the protuberance is consistent with this structure replacing the tail bud (Figure 4Ac-d). A structure protruding posteriorly from the PS of Snai1-cKO embryos was already visible at E8.25 as a bulge (Figure 5 and Figure 5—video 1), when the embryo was building trunk structures. At this stage, Lfng expression in Snai1-cKO embryos showed variable expression patterns in the region anterior to the bulge, consistent with cycling activity in the presomitic mesoderm generating trunk somites (Figure 5Ac and Figure 5—figure supplement 1). Interestingly, variable Lfng signal was also observed in the bulge. To better characterize the apparently variable Lfng expression in the bulge we introduced the LuVeLu reporter transgene (Aulehla et al., 2008), which allows live imaging of Lfng cycling activity, into the Snai1-cKO background. Two-photon live imaging analysis of LuVeLu::Snai1-cKO embryos confirmed the rather normal cyclic activity associated with trunk somite formation and revealed the existence of additional LuVeLu waves in the bulge as a signal moving posteriorly through its dorsal surface (Figure 6 and Figure 6—videos 1, 2). Therefore, Lfng also shows cycling activity in the bulge but with spatial and directional features different from those observed in wild type and more anterior embryonic regions of the mutant embryos, where it runs from posterior to anterior through the more ventrally located presomitic mesoderm. Together, these results indicate that the PS and the bulge represent different functional modules and that Snai1 is required for secondary but not postcranial primary body formation.

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Snai1-cKO embryos develop an ectopic bulge associated with the PS.

(A) Wholemount in situ hybridization with the indicated markers in wild type (WT) and Snai1-cKO mutant embryos at E8.5. The inlets show close ups of the caudal region. Transverse sections at the levels indicated in the whole-mount embryo are also shown. In the absence of Snai1, a protuberance (black arrowheads) starts to arise from the PS around E8.25. This ectopic bulge is positive for Lfng and Nkx1-2, but not for Sox2. Lfng and Nkx1-2 expression are restricted to the epithelial-part of the bulge. Msng1 was only found in the mesenchymal component. (B) 3D reconstruction of E8.5 Snai1-cKO and wild type posterior/caudal structures: neural tube (green), open epiblast (light green), presomitic mesoderm (light blue), somites (dark blue), notochord (red) and endoderm (yellow). At E8.5, Snai1-cKO embryos contain an ectopic bulge (black arrowhead) associated with the PS and the hindgut endoderm shows abnormal development.

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3D two-photon live imaging of LuVeLu reporter expression in E8.5 Snai1-cKO and control embryos.

(A) Snapshot at time-point = 0 of the LuVeLu reporter, in Snai1-cKO (from Figure 6—video 1) and control (from Figure 6—video 2) E8.5 embryos. In addition to the normal LuVeLu signal in the presomitic mesoderm, Snai1-cKO embryos display ectopic LuVeLu expression in the epithelial-like component of the bulge. (B) Snapshots from Figure 6—video 1 and Figure 6—video 2, of time-lapsed two-photon live imaging of the LuVeLu reporter in E8.5 Snai1-cKO and control embryos at the indicated time points. Snai1-cKO embryos have ectopic LuVeLu expression in the epithelial-like component of the bulge in addition to the normal LuVeLu signal in the presomitic mesoderm. (C) Quantitative analysis of LuVeLu cycling activity in the bulge of Snai1-cKO embryos. Intensity mean was calculated in the region highlighted by the blue spot (Ca) and plotted for each imaged time-point (8.5 min interval; Ca’). The existence of two-peaks (at t = 1.3 hr and t = 3.6 hr of the time-lapse) and a substantial decrease between them, suggests cycling activity in the bulge of the mutant embryo. These waves occur from anterior to posterior, once the higher intensity mean peak observed in the posterior part of the bulge (red spot; Cb) occurred later than the higher peak measured in the anterior part of the bulge (green spot; Cb). The higher measured wave peak in the posterior part of the bulge (red spot; Cb) coincides with the time-point corresponding to the higher intensity mean peak detected in the newly formed somite (yellow spot; Cc). No signs of LuVeLu cycling activity were observed near the PS (purple spot; Cd) in LuVeLu+/0 control embryos. Scale bar: 50 μm.

The protuberance observed in Snai1-cKO embryos consisted of an epithelial-like layer extending posteriorly from the trunk neural tube, covering a mass of mesenchymal tissue contiguous with the trunk paraxial mesoderm (Figure 3, Figure 3—video 1 and Figure 5, Figure 5—video 1). At E9.5, the notochord was either bifurcated or had reversed its direction of growth (2 and 6 embryos respectively) becoming associated with gut endodermal tissue that fails to extend into the protuberance and is often detached from the rest of the embryonic tissues (found in 12 from the 19 embryos in which this feature was explored) (Figure 3Ao-r’, Au-v’ and B). At this stage, Sox2 mRNA expression was detected in the trunk neural tube of Snai1-cKO embryos but failed to extend into the epithelial component of the bulge (Figure 3As-t). This suggests that, despite histological continuity, the bulge’s epithelial sheet is most likely not an extension of the trunk neural tube. Interestingly, at E9.5 this epithelium contained Sox2 protein [likely resulting from significantly higher protein than transcript stability (Aires et al., 2016)] in cells also expressing T (Figure 7), thus fitting the T+/Sox2+NMP molecular signature. The axial progenitor identity of the cells within this epithelium was further supported by the prominent expression of a variety of NMP-related genes (Aires et al., 2018; Rodrigo Albors et al., 2018; Gouti et al., 2017; Wymeersch et al., 2019), including T, Wnt3a, Fgf8, Nkx1-2 and Cyp26a1 (Figure 3A). Interestingly, Fgf8 and Nkx1-2 expression, as well as T+/Sox2+ cells, were highly restricted to the bulge’s epithelial layer, which contrasts with their extension into the nascent mesenchyme in wild type embryos when they enter the tail bud stage (Figure 3A and Figure 7). These observations suggest that in the absence of Snai1, NMPs become trapped in the epithelial layer of the protuberance, failing to complete the trunk-to-tail transition and disrupting secondary body formation.

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T and Sox2 double-positive cells are restricted to the epiblast of Snai1-cKO embryos.

Wholemount immunostaining for T (green), Sox2 (red) and DAPI (blue) in E9.5 (A and B) series) and E10.5 (C and D) series) Snai1-cKO and wild type (WT) embryos. Transversal and sagittal optical sections together with magnifications (Mag.) are also shown. In E9.5 wild type embryos, T+/Sox2+ cells are found in the mesenchyme below the epiblast (white arrows). Conversely, in similar staged Snai1-cKO embryos, they are restricted to the epithelial component of the bulge. At E10.5 most of the bulge’s epithelium, of Snai1-cKO embryos, closed into a tube that is mostly negative for Sox2 and positive for T. In contrast, T and Sox2 double-positive cells are still found in mesenchymal compartments of the tail bud of wild type embryos. Magnifications are shown without DAPI. Scale bars correspond to 50 μm.

The mesenchymal component of the bulge was positive for paraxial mesoderm markers, including Tbx6 or Msgn1, but negative for lateral mesoderm markers such as Tbx4 (Figure 3Ak-n’, Figure 4A and Figure 5Ac-d’), thus resembling paraxial mesodermal features. Moreover, Tbx6 expression was not restricted to the bulge’s mesenchyme but was also observed in the epithelium (Figure 3Ak-l’, and Figure 8B). Since a portion of tail bud NMPs are positive for Tbx6 expression (Javali et al., 2017), it is possible that the bulge’s epithelial component contains progenitor cells that have already acquired some of the mesenchymal traits associated with tail bud axial progenitors. Consistent with this hypothesis, we only detected residual Cdh1 and Epcam expression in the bulge epithelium at E9.5, whereas expression of mesenchymal markers such as Cdh2 and Vim were readily detectable at levels comparable to those in wild type embryos (Figure 8A and Figure 8—figure supplement 1). In addition, Laminin1 expression in the bulge’s epithelium was highly disorganized already at E8.5, contrasting with the characteristic epithelial pattern observed in adjacent more anterior areas of the same embryos or in the epiblast of wild type littermates (Figure 8B). Together, these observations indicate that in the absence of Snai1 axial progenitors initiate tb-EMT and acquire some mesenchymal features but are unable to complete the transition to tail bud development.

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Axial progenitors acquire mesenchymal properties in the absence of Snai1.

Wholemount immunostainings for Cdh1 (green) plus Cdh2 (red) (A) and Tbx6 (green) plus Lam1 (red) (B), in E8.5 and E9.5 Snai1-cKO and wild type (WT) embryos. Transversal and sagittal optical sections in the indicated regions are also shown together with magnifications (Mag.). The transition from Cdh1 to Cdh2 still occurs in the epithelial component of the bulge in the absence of Snai1 (white arrows). This region of Snai1-cKO embryos contains ectopic Tbx6-positive cells (yellow arrow) and a severely disorganized Lam1 expression (white arrowheads). Yellow arrowheads highlight posterior gut bifurcation in E9.5 Snai1-cKO embryos. Scale bars: 50 μm. DAPI staining in blue.

Snai1 and Tgfbr1 cooperatively orchestrate the transition from primary to secondary body formation

Gdf11 has been associated with the trunk-to-tail transition (Aires et al., 2016; Jurberg et al., 2013; Liu, 2006; Matsubara et al., 2017). However, its partial functional redundancy with Gdf8 in this process (McPherron et al., 2009; McPherron et al., 1999) hinders proper evaluation of its contribution to tb-EMT. Nevertheless, genetic experiments indicate that Gdf11 (and most likely Gdf8) activity in the caudal embryo is mediated by Tgfbr1 (also known as Alk5) (Andersson et al., 2006; Jurberg et al., 2013), a known EMT regulator (Derynck et al., 2014; Xu et al., 2009) that is expressed in areas containing axial progenitors (Figure 2—figure supplement 2), thus making Gdf11/Tgfbr1 signalling a prime candidate to play a role in tb-EMT. To overcome Gdf11/Gdf8 functional redundancy, we therefore generated Tgfbr1 mutant embryos. Initial analysis of Tgfbr1-/- embryos confirmed the role of this receptor as an inducer of the trunk-to-tail transition (Figure 9), and also indicating the absence of redundancy from other type I receptor of the Tgfβ/BMP gene family in this process. Indeed, these mutant embryos extended their axis through the trunk region but failed to undergo the transition to tail development, as illustrated by absent hind limb bud markers, lack of Lin28a expression at E10.5, which is involved in promoting tail bud axial progenitor activity (Aires et al., 2019; Robinton et al., 2019), and only residual activation of posterior genes like Hoxc10 (Figure 9). In addition, the anterior-ventral relocation of the allantois -as the embryo turns and starts developing umbilical structures at tail bud stages- was compromised in these mutant embryos and all tested NMP markers (e.g. T, Fgf8 and Cyp26a1) seemed to stay associated with dorsal tissues, with no sign of contribution to tail bud mesenchyme/mesodermal tissue (Figure 9G–L). Together, these observations are consistent with the embryos finishing their axial extension when Pou5f1 stops influencing axial progenitor activity derived from its natural decay (Osorno et al., 2012), as they are unable to activate the trunk-to-tail transition.

Figure 9
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Tgfbr1 mutant embryos are unable to undergo the trunk-to-tail transition.

(A–N) Wholemount in situ hybridization with the indicated markers in E10.5 Tgfbr1-/- and wild type (WT) embryos. Absent hindlimb bud formation in Tgfbr1 mutants is highlighted by absent Tbx4, Fgf8 and Hoxc10 expression (A–D, G and H) in the relevant area (white arrows). Tail bud formation is deficient in Tgfbr1 mutant embryos (black arrows). Lin28a and T are drastically downregulated in the tail of Tgfbr1 mutant embryos (black arrows in E and I), suggesting that these mutants are caudally truncated at this stage. The white arrowheads indicate the notochord, which did not continue its development to more caudal regions in Tgfbr1 mutant embryos. Red arrowheads highlight the abnormal Cyp26a1 expression in the Tgfbr1-/- tail. Red arrows in M) and N) indicate absent Isl1 expression in the prospective developing cloaca of Tgfbr1 mutant embryos.

In Tgfbr1-/- embryos the transition from Cdh1 to Cdh2 in the posterior embryo was very inefficient, as Cdh1 was still detected in the Tgfbr1-/- epiblast at E9.5 and Cdh2 was only detected at very low levels (Figure 10A). Concomitantly, we observed the characteristic Laminin1 epithelial patterns, as well as higher Epcam and lower Vim levels in the Tgfbr1 mutant epiblast than in similar stage control embryos (Figure 10B and Figure 10—figure supplement 1). These data support an essential role for Gdf11/Tgfbr1 signalling in triggering tb-EMT and suggest that this signalling activity precedes that of Snai1 during tb-EMT. However, contrary to what has been described in other experimental contexts (Lamouille et al., 2014), Snai1 is most likely not a direct target of Tgfbr1 signalling during tb-EMT, as we did not find any evidence for increased Snai1 expression in the progenitor-containing region of Tgfbr1-overexpressing embryos [Cdx2-Alk5CA transgenics (Jurberg et al., 2013; Figure 11B)]. This suggests that Snai1 and Gdf11/Tgfbr1 signalling are part of independent pathways that converge to orchestrate the tb-EMT. Indeed, Snai1 expression in the PS region covers only a small region within the Gdf11 expression domain in the epiblast (Hernández-Martínez et al., 2019; Nieto et al., 1992; Figure 11A). Therefore, it is possible that Snai1 marks a subset of axial progenitors within the cell pool exposed to Gdf11/Tgfbr1 signalling to be recruited to the tail bud by entering tb-EMT.

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Tail bud EMT is compromised in the absence of Tgfbr1.

Wholemount immunostaining for Cdh1 (green) plus Cdh2 (red) (A) and Epcam (green) plus Vim (red) (B) in Tgfbr1-/- and wild type (WT) embryos. Transversal and sagittal optical sections through the indicated regions are also shown together with magnifications (Mag.). White arrowheads indicate incomplete Cdh1 to Cdh2 switch in Tgfbr1 mutants. White arrows show persistent Epcam and deficient Vim expression in the epithelium of the mutant embryos. DAPI staining is shown in blue. Scale bars: 50 μm.

Figure 11
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Snai1 is not a downstream target of Tgfbr1.

(A) Wholemount in situ hybridization for Gdf11 in E8.25, E8.5 and E9.5 wild type (WT) embryos. Transversal sections through the areas indicated in the whole mounted embryo highlight the increase of Gdf11 in caudal tissues during primary body formation. (B) Overexpression of a constitutively active form of Tgfbr1 (transgenic Cdx2-Alk5CA) does not result in increased Snai1 expression as shown in transversal sections of the areas indicated in the wholemount embryo. Arrows indicate the position of the PS, where low levels of Snai1 expression can be observed both in the WT (Bb) and transgenic embryos (Ba).

Extended Snai1 expression in the PS mobilizes functional tail bud progenitors

A prediction from this hypothesis is that expanding the Snai1 expression domain in the PS would lead to an increase in the number of cells entering the tail bud route. We tested this hypothesis using a transgenic approach expressing Snai1 under the control of the T-str enhancer (Clements et al., 1996), a regulatory element of the Brachyury gene that drives expression in progenitor cells within the PS (Anderson et al., 2013). About half of these transgenic embryos (n = 43) showed caudal morphological abnormalities at E9.5, including axial shortening and premature closure of the caudal neuropore (Figure 12). In these embryos the T, Cyp26a and Nkx1.2 domains expanded into the ventral mesenchymal region of the shortened tail bud (Figure 12C-D2, I-L2), consistent with production and delamination of tail bud axial progenitors in regions more anterior to the normal position of the tail bud. In addition, these embryos had a variable number of ectopic neural tubes connected caudally with the expanded Nkx1.2-positive mesenchymal domain, aligning ventrally to the main spinal cord (Figure 12), which is consistent with these cells having acquired tail bud NMP identity. We also found cells expressing T and Tbx6 intermingled with these ectopic neural tubes (Figure 12C1–C2, M1), further supporting the NMP identity of these progenitors. Interestingly, these extra neural tubes contained a degree of dorso-ventral patterning, as shown by Foxa2 expression in their ventral domain, corresponding to the floor plate (Figure 12O1), and by Wnt3a expression in the dorsal part of some of these ectopic neural tubes (Figure 12G1). Together, these results indicate that Snai1 is necessary and sufficient for axial progenitor mobilization during tail bud formation.

Figure 12
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Extended Snai1 expression in the PS is sufficient to mobilize axial progenitors from the epiblast.

(A–R) Wholemount in situ hybridization for the indicated markers in wild type (WT) and transgenic T-str-Snai1 embryos. Nkx1-2 expression in the transgenic embryos (A) indicates an already deformed caudal epiblast at E8.5. At E9.5 T-str-Snai1 embryos are caudally truncated and display a complete premature closure of their caudal epiblast. Red arrows in C2, I1 and K1 highlight the ventrally extended T, Cyp26a1 and Nkx1-2 expression, indicating ectopic mobilization of axial progenitors. Black arrows in E1 and K2 show ventrally located ectopic neural tubes in T-str-Snai1 embryos. Red arrows in C1 and M1 indicate T, Tbx6-positive cells intermingled with the ectopic neural tubes. The black arrowheads in O1 and P1 indicate the floor plate, showing conserved ventral patterning in ectopic neural tubes of T-str.Snai1 embryos. The red arrowheads in G1 show Wnt3a expression in the dorsal region of the ectopic neural tubes.

Discussion

The transition from primary to secondary body formation involves at least two coordinated but independent processes. One such process entails activation of a terminal differentiation program in the progenitors for the intermediate and lateral components of the mesoderm that results in the induction of the hindlimb bud and of the mesodermal component of the cloaca (Jurberg et al., 2013). The second process involves the common progenitors for the spinal cord and paraxial mesoderm that become the tail bud, from where they promote further extension of the body axis to generate post-sacral body structures (Henrique et al., 2015; Steventon and Martinez Arias, 2017; Wilson et al., 2009).

Snai1 and Tgfbr1 play a key role in the gene regulatory networks driving tail bud formation

Genetic experiments have shown that Gdf11 plays an important role in both processes by activating signalling in the axial progenitors through the Tgfbr1 receptor. Indeed, premature activation of this signalling in axial progenitors anticipates the trunk-to-tail transition (Jurberg et al., 2013; Liu, 2006; Matsubara et al., 2017), and Tgfbr1 null embryos are unable to engage in tail development (this work).

A variety of experimental evidence indicates that Isl1 is a key component of the network downstream of Tgfbr1 to induce hindlimb and cloacal tissues (Jurberg et al., 2013). The same experiments also showed that this gene is not involved in tail bud formation, indicating the existence of a different mechanism regulating the formation of this structure. Here we presented evidence for the critical role of Snai1 in this process. Interestingly, however, this gene is not under the control of Tgfbr1 signalling but provides instead a parallel activity that promotes segregation of axial progenitors into the future tail bud upon functional convergence with Tgfbr1 signalling. The Snai1-cKO mutant phenotype indicates that tail bud formation starts rather early in development when the embryo is still actively engaged in PS-mediated trunk development, much earlier than the appearance of morphological signs of a tail bud. This phenotype thus uncovers the existence of a functional developmental module specifically devoted to the formation of the tail bud, independent from that involved in trunk formation. The existence of such ‘tail bud module’ somehow resembles hindlimb or cloacal induction, thus suggesting a unifying mode by which Gdf11/Tgfbr1 signalling activity triggers the different processes involved in the trunk-to-tail transition, consisting in activating alternative developmental programs in different subsets of axial progenitors. The observation that NMPs are suppressed by Isl1 activity (Jurberg et al., 2013) indicates that the intrinsic properties of these cells differ from those of the progenitors for intermediate and lateral mesoderm, determining whether they engage in tail bud or hindlimb/cloaca formation upon Tgfbr1 functional input.

Different experimental observations indicate that trunk length and the position of the switch from trunk to tail developmental modes result from quantitative functional balance between Gdf11 and Pou5f1 activities (Aires et al., 2016; DeVeale et al., 2013; Jurberg et al., 2013; Mallo, 2018). These observations, together with the Snai1-cKO mutant phenotype lead us to suggest a model for axial extension whereby at early stages (mouse E8.0) progenitor activity is dominated by Pou5f1, keeping an active PS, while Gdf11/Tgfbr1 functional contribution is negligible or extremely small. As development proceeds Pou5f1 activity is progressively reduced in the epiblast (Osorno et al., 2012) and Tgfbr1 acquires increased functional weight in this area. Snai1-positive cells in the PS are the first to respond to the reversed Pou5f1/Tgfbr1 activity balance, resulting in NMPs mobilizing to the tail bud. This process is already triggered when the PS still actively coordinates development at more anterior levels, indicated by the Snai1-cKO phenotype. As development proceeds, Pou5f1 activity decreases (Osorno et al., 2012), and given its requirement for PS maintenance (Aires et al., 2016; DeVeale et al., 2013), it is likely to be responsible, together with Snai1, for PS regression and caudal epiblast closure. Under these conditions, Tgfbr1 eventually takes full control of axial progenitor activity, leaving the tail bud as the only source of axial extension activity and recruiting lateral mesoderm progenitors into hindlimb and cloacal structures. In addition, this model implies an overlap of primary and secondary processes of neural tube formation, and therefore fits better with classical observations in human embryos (Saitsu et al., 2004). A failure in the coordination between these two processes can ultimately lead to the generation of spina bifida (Saitsu and Shiota, 2008).

Two different functional types of EMT are required during vertebrate axial extension

Here we have shown that the transition from primary to secondary body formation in the mouse entails an incomplete EMT acting on axial progenitors and termed this new developmental process ‘tail bud EMT’ (tb-EMT), as it is required for tail bud formation. This EMT is different from that driving epiblast progenitors through the PS to generate mesodermal tissues during gastrulation in different ways. (1) progenitors undergoing tb-EMT do not enter a differentiation route but retain instead progenitor properties that endow them with the capacity to further extend the body axis by generating both the neural tube and paraxial mesoderm of the tail. (2) tb-EMT is incomplete, keeping expression of a subset of epithelial markers that leave the progenitors in a transitional state. This property might actually facilitate the production of both neural and mesodermal structures from tail bud axial progenitors. Moreover, it is possible that maintenance of some epithelial properties can help progenitors to keep contact with the trunk neural epithelium that they will eventually extend by regaining full epithelial features. Conversely, these cells would be able to enter mesodermal differentiation routes just by completing the EMT, thus circumventing the need for a functional PS. Interestingly, comparison of CNH and tail bud mesenchyme heterochronic grafts (Cambray and Wilson, 2002) showed that after tail bud progenitors enter the mesodermal compartment, they have no longer the potential to generate neural tissues, becoming restricted to mesodermal compartments, further supporting that tail bud progenitors are kept in a transitory state instead of acquiring full mesenchymal characteristics when entering the tail bud.

Another major difference between gastrulation- and tail bud- associated EMTs resides in their genetic control. Genetic experiments identified a number of genes involved in early gastrulation steps, including Crumbs2, p120-catenin, Eomes, Nodal and FGF signalling (Arnold et al., 2008; Deng et al., 1994; Hernández-Martínez et al., 2019; Ramkumar et al., 2016; Voiculescu et al., 2014; Yamaguchi et al., 1994). Tgfbr1, which is an essential component of tb-EMT, is clearly not involved in gastrulation as embryos lacking this receptor can go through this developmental step and remarkably generate trunk structures. Snai1 seems to be required for both gastrulation and tb-EMT, although its role might be different in both processes. Snai1 null mutant embryos generate mesoderm during gastrulation but the mesodermal cells produced are unable to complete their EMT process, keeping several epithelial characteristics and failing to downregulate Cdh1 (Carver et al., 2001). During tb-EMT cells lacking Snai1 had already lost several epithelial characteristics, most likely resulting from a previous Tgfbr1 functional input, suggesting that its role during tail bud formation must be different from that in gastrulation. In Snai1-cKO embryos, axial progenitors were restricted to epithelial-like layer of the bulge contiguous with the posterior epiblast. Conversely, these cells seem to leave the epiblast prematurely in T-str-Snai1 transgenic embryos. Therefore, although the role of Snai1 in tail bud formation requires further evaluation, it is possible that it might be involved in cell mobilization. Interestingly, the phenotypes of both Snai1 null and of Snai1-cKO mutant embryos suggest that PS activity during postcranial elongation is functionally different to that during early gastrulation because Snai1-cKO embryos are able to efficiently elongate the postcranial primary body even in the absence of detectable Snai1 (Murray and Gridley, 2006). This observation is in keeping with a large body of genetic data indicating differences in the gene networks regulating early gastrulation processes and postcranial axial elongation (Andre et al., 2015; Herrmann et al., 1990; Liu et al., 1999; Savory et al., 2011; Takada et al., 1994).

It should be also noted that tb-EMT functional and molecular characteristics are more akin to those described for the transitions involved in metastatic processes than to the typical developmental EMTs (e.g. gastrulation) (Acloque et al., 2009; Kalluri and Weinberg, 2009; Lamouille et al., 2014; Nieto et al., 2016). These transient tail bud progenitors might not only be used to re-assess neural tube closure defects, but also represent a novel in vivo model to study the mechanisms activating Tgfbr1/Snai1-dependent metastatic processes.

Materials and methods

Key resources table
Reagent type
(species) or resource		DesignationSource or referenceIdentifiersAdditional information
Gene
(M. musculus)		Snai1MGIMGI:98330(other names) Snail
Gene
(M. musculus)		Tgfbr1MGIMGI:98728(other names) Alk5
Genetic reagent
(M. musculus)		B6.1239S4-Meox2tm1(cre)Sor/JJackson LabsStock No 003755
RRID:IMSR_JAX:026858		Tallquist and Soriano, 2000
(another name Meox2-Cre+/0)
Genetic reagent
(M. musculus)		B6.129S-Snai1tm2Grid/JJackson LabsStock No 010686
RRID:IMSR_JAX:010686		Murray and Gridley, 2006
(another name Snai1flox/flox)
Genetic reagent
(M. musculus)		LuVeLuAulehla et al., 2008Transgenic
Genetic reagent
(M. musculus)		T-str-Snai1This paperTransgenic
Genetic reagent
(M. musculus)		Tgfbr1+/-This paperTargeted null mutation
Genetic reagent
(M. musculus)		Cdx2-Alk5CAJurberg et al., 2013Transgenic
Antibodyanti-Brachyury (Goat polyclonal)R and D SystemsAF2085
RRID:AB_2200235		IF (1:200)
AntibodyAnti-Sox2
(Rabbit monoclonal)		Abcamab92494
RRID:AB_10585428		IF (1:200)
Antibodyanti-Cdh1
(Goat polyclonal)		R and D SystemsAF648
RRID:AB_355504		IF (1:200)
Antibodyanti-Cdh2
(Rabbit polyclonal)		Abcamab18203
RRID:AB_444317		IF (1:200)
Antibodyanti-Tbx6
(Goat polyclonal)		R and D SystemsAF4744
RRID:AB_2200834		IF (1:200)
Antibodyanti-Laminin 111 (Rabbit polyclonal)SigmaL9393
RRID:AB_477163		IF (1:200)
AntibodyEpCAM/TROP1 (Goat polyclonal)R and D SystemsAF960
RRID:AB_355745		IF (1:200)
Antibodyanti-Vimentin
(Rabbit monoclonal)		Abcam,ab92547
RRID:AB_10562134		IF (1:200)
Antibodyanti-goat 488
(Donkey polyclonal)		Molecular ProbesA11055
RRID:AB_2534102		IF (1:1000)
Antibodyanti-rabbit 568
(Donkey polyclonal)		ThermoFisher ScientificA10042
RRID:AB_2534017		IF (1:1000)
Recombinant DNA reagentT-str promoterClements et al., 1996Primitive streak-specific promoter of T (Brachyury)
Recombinant DNA reagentSnai1 cDNANieto et al., 1992
Sequenced-based reagentOligonucleotidesThis paperTable 1
Commercial assay, kitNextera XT index kit v2 Set BIlluminaFC-131–2002
Commercial assay, kitLibrary Quant KitIlluminaLC480
Commercial assay, kitKAPA Library Quantification KitsKAPA BiosystemsKK4854
Software, algorithmSC3Kiselev et al., 2017RRID:SCR_015953
Software, algorithmSPRINGWeinreb et al., 2018

Mouse lines

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Meox2-Cre+/0 (Tallquist and Soriano, 2000) and Snai1flox/flox (Murray and Gridley, 2006) mouse strains were obtained from Jackson labs (B6.129S-Snai1tm2Grid/J – Stock No 010686; B6.1239S4-Meox2tm1(cre)Sor/J – Stock No 003755). The LuVeLu reporter strain (Aulehla et al., 2008) was provided by Alexander Aulehla and Olivier Pourquié. Snai1-cKO embryos (Meox2-Cre+/0::Snai1flox/-) were obtained by crossing Meox2-Cre+/0::Snai1+/- males with Snai1flox/flox females. Meox2-Cre+/0::Snai1flox/-::LuVeLu+/0 embryos were obtained from similar crosses but with the LuVeLu reporter introduced into Snai1flox/flox genotype.

To obtain T-str-Snai1 transgenic embryos, constructs were prepared by cloning a ~ 1,5 kb Snai1 cDNA (Nieto et al., 1992) under the control of the PS-specific promoter of T (Brachyury)(Clements et al., 1996). These constructs were liberated from vector sequences, gel purified and used to produce transgenic embryos by pronuclear injection in FVB/N fertilized oocytes according to standard procedures (Hogan et al., 1994).

The Tgfbr1+/- line was generated by CRISPR/Cas9, inserting the TGATGATAGGATCC sequence, containing three stop codons and a BamHI restriction site in frame with the open reading frame in exon 2. For this, a gRNA containing the targeting sequence TTGACCTAATTCCTCGAGAC was produced by in vitro transcription with the T7 promoter from a plasmid derived from the gRNA-basic (Casaca et al., 2016). The purified gRNA was microinjected into fertilized FVB/N mouse oocytes together with the Cas9 mRNA and the synthetic ssDNA 5’-ACCACAGACAAAGTTATACACAATAGTATGTGTATAGCTGAAATTGACCTAATTCCTCGATGATGATAGGATCCGACAGGCCATTTGTATGTGCACCATCTTCAAAAACAGGGGCAGTTACTACAACATATTGC-3’, containing the stop codons flanked by 60 nucleotide-long homology arms. Genotyping of embryos was performed by PCR, on DNA obtained from yolk sacs or tail biopsies from embryos or mice, respectively, as previously described (Aires et al., 2019). The primers used for genotyping are specified in Table 1.

Table 1
Primers used for genotyping.
Snai1 deletion FwdCGGGCTTAGGTGTTTTCAGAC
Snai1 deletion RevTGAAAGCGGCTCTGTTCAGT
Snai1flox FwdTGAAAGCGGCTCTGTTCAGTG
Snai1flox RevCTGCTGCACCCCTACTATGTG
Meox2-Cre FwdCGAGTGATGAGGTTCGCAAG
Meox2-Cre RevCCTGATCCTGGCAATTTCGGCT
LuVeLu FwdTGCTGCTGCCCGACAACCACT
LuVeLu RevCTTGTACAGCTCGTCCATGCC
Snai1 transgenics FwdTTGTGTCTGCACGACCTGTGG
Snai1 transgenics RevATGGGGAGGTAGCAGGGTCAG
Tgfbr1 FwdTGTGAGACAGATGGTCTTTGC
Tgfbr1 mutant allele RevGGCCTGTCGGATCCTATCATC
Tgfbr1 WT allele RevACATACAAATGGCCTGTCTCG

Ethical statement

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Experiments involving animals carried out in the Oeiras laboratory followed the Portuguese (Portaria 1005/92) and European (Directive 2010/63/EU) legislations, concerning housing, husbandry, and welfare. The project was reviewed and approved by the Ethics Committee of ‘Instituto Gulbenkian de Ciência’ and by the Portuguese National Entity, ‘Direcção Geral de Alimentação Veterinária’ (license reference: 014308).

Single cell isolation

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Wild type outbred MF1 mice were crossed to obtain early head fold embryos. Caudal lateral epiblast (CLE, comprising a region immediately lateral to the posterior edge of the node and lateral to the primitive streak, extending to about half the length of the primitive streak) (Wymeersch et al., 2016) was microdissected in M2 medium (Sigma, M7167), using hand-pulled solid glass needles. After removal of the majority underlying paraxial mesoderm, the different tissue pieces were pooled and after 5 min at 37°C in 0.05% trypsin/EDTA, they were placed in neutralization solution [10% fetal calf serum in phosphate-buffered saline (PBS)] and dissociated by pipetting into single cells. Single cells were then transferred to a tube containing 2% FCS in PBS, strained through the 35 µm mesh of a FACS tube (Corning, 352235) and 1 μg/ml of 4',6-Diamidino-2-Phenylindole, Dihydrochloride (DAPI; Thermo Fisher Scientific, D1306) was added. Single-cells were sorted by Fluorescence-activated cell sorting FACS) with a FACS Aria II (BD Biosciences) into individual wells of a 96-well PCR plate (BioRad, HSS9601) containing the ERCC RNA spike-in Mix (Ambion, #4456740) diluted (1:100.000) in a solution of 0,2% Triton-X100 (vol/vol) (Sigma, T9284), containing 2 U/ µl of RNase inhibitor (Takara Bio Europe, #2313A), 25% (v/v) of 100 μM oligo dT30VN (Biomers) and 25% (v/v) of dNTPs 10 mM (Invitrogen, #18427013) into RNAse-free H20 (Thermo Fisher Scientific, 11430615). Plates were sealed with Microseal F (Biorad, MSF1001), centrifuged at 4°C for 1 min at 2000 rpm and stored at −80°C.

Single-cell RNA sequencing

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Full-length RNA-seq from sorted single cells was done using the Smart-seq2 method (Picelli et al., 2014). Libraries from a total of 91 single cells were prepared using a Nextera XT index kit v2 Set B (Illumina) and quantified both using Library Quant Kit (Illumina - LC480, KAPA Biosystems - KK4854) and the AATI Fragment Analyzer. Sequencing was done at the IGC Genomics facility (Illumina, Nextseq 500) at 5 million single end 75 bp reads per cell.

Single-cell RNA-seq analysis

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RNA-seq analysis was done using R software. Sequences were submitted to the GEO repository, accession number GSE147100. Raw sequences were aligned to the GRCm38 (mm10) reference genome using Hisat2 (Kim et al., 2013). The ‘featureCounts’ R function was used to count reads mapping to annotated genes. Clustering analysis was done using the single-cell consensus clustering (SC3) pipeline (Kiselev et al., 2017). Gene markers were obtained considering p-value<0,05. P-values are shown in Spreadsheet 1. Single-cell data visualization was done using SPRING (Weinreb et al., 2018), with the following parameters: Minimum UMI total (for filtering cells)=1000; Minimum number of cells with >= 3 counts (for filtering genes) was set to 3; Gene variability percentile (for filtering genes)=50; Number of PCA dimensions (for building graph) was set to 20; Number of nearest neighbours (for graph)=5. Single cell heatmaps were created using the Heatmapper platform (Babicki et al., 2016). The scRNA-seq values in RPKM used for this analysis are shown Spreadsheet 2.

In Situ hybridization and sectioning

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Wholemount in situ hybridization was performed as previously described (Aires et al., 2019). These experiments were repeated independently at least twice for each genotype giving identical results, with the exception of Lfng, which gave different patterns in the PSM region as reported in Figure 5 and Figure 5—figure supplement 1, and notochord markers in Snai1-cKO embryos, that gave two alternative patterns as referenced in the main text. Post-stained embryos were included in a mixture of 0.45% gelatin (Merck), 27% bovine serum albumin (Roche), 18% sucrose (Sigma) in PBS that was then jellified with 1.75% glutaraldehyde (Biochem chemopharma) and sectioned at 20 μm with a vibratome (Leica).

Immunohistochemistry and 3D imaging

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Wholemount immunofluorescence staining of tail tissues was performed as previously described (Osorno et al., 2012). At least two embryos per genotype were stained with each antibody with similar results. Primary antibodies (1:200): goat anti-Brachyury (R and D Systems, AF2085), rabbit anti-Sox2 (Abcam, AB92494), goat anti-Cdh1 (R and D Systems, AF648), rabbit anti-Cdh2 (Abcam, AB18203), goat anti-Tbx6 (R and D Systems, AF4744), rabbit anti-Laminin 111 which detects all laminins containing a1, b1 or g1 chains (Sigma, L9393), goat anti-human EpCAM/TROP1 (R and D Systems, AF960) and rabbit anti-Vimentin (Abcam, AB92547). Secondary antibodies (1:1000): donkey anti-goat 488 (Molecular Probes, A-11055) and donkey anti-rabbit 568 (Molecular Probes, A10042). Immuno-stained tails were imaged on a Prairie two-photon system, using an Olympus 20 × 1.0 NA W objective, with the excitation laser tuned to 960 nm, and GaAsP photodetectors. Z stacks of 1024 × 1024 images were acquired every 1 μm, with either 1x or 1.5x zoom. Laser intensity and photomultiplier levels were maintained across replicates and controls.

Live imaging (LuVeLu)

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Embryos expressing the LuVeLu reporter (Aulehla et al., 2008) were dissected in pre-warmed (at 37°C) M2 medium (Sigma) and cultured in low glucose DMEM medium (Gibco, 11054020), 10% of HyClone defined fetal bovine serum (GE Healthcare, #HYCLSH30070.03), 2 mM of L-glutamine (Gibco,#25030–024) and 1% penicillin-streptomycin (Sigma, #P0781). Embryos were cultured at 37°C in a 65% O2 and 15% CO2 environment (N2 balanced). Embryos were imaged on the Prairie two-photon system (laser tuned to 960 nm). At time = 0, a z-stack of 5 μm step-size was acquired at 1024 × 1024 pixel size, using the 20x objective. From t = 1 and onwards, we acquired z-stacks series of 1024 × 512 pixel images, spaced in depth at 10 μm, using a Nikon 16x LWD 0.8NA W objective. T-series were acquired every 8,5 min.

Image processing

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3D and 4D series of two-photon microscopy datasets were processed using Fiji (Schindelin et al., 2012). Pre-processing involved removal of outlier pixels and elimination of electronic noise in the form of periodic patterns by using fast-Fourier filters (detection of ‘maxima’ in the Fourier spectrum and deleting for each an area with r = 5 pixels, performed slice-by-slice). 3D datasets of immuno-stained tissues were deconvolved using Huygens (SVI). When acquired, adjacent 3-stack datasets were digitally stitched using the ‘Image Stitching’ plugin (Preibisch et al., 2009) (pairwise mode, with alpha blending). We then evaluated the Z-axis attenuation in 3D datasets; when attenuation in depth was noticeable we performed a compensation using FIJI’s ‘Math...Batch’ function and the expression: v = v * exp (a * z), where v = pixel intensity; a = compensation factor (ranging from 1 to 2, depending on the compensation necessary to equalize the intensities on the first and the deeper optical slices) – replicates and controls were treated similarly. The pre-processed multi-channel dataset was then repositioned by affine transformation using the ‘TransformJ’ plugin (Meijering et al., 2001). The transformation matrix was obtained using FIJI’s 3D viewer plugin. 3D visualization and analysis of embryo tails was done using Imaris v9.0 (Bitplane), including the rendering of wholemount (blend mode) and of sagittal and transversal 5 μm optical sections by maximum intensity projection. Note: In EPCAM-stained samples, a considerable bleed-through from the DAPI channel was observed. Therefore, before deconvolution, the EPCAM channel was compensated by dividing it by the DAPI signal. Further background reduction was achieved by dividing the compensated dataset by a ‘synthetic background’ obtained from optical slices without stained tissue. Mutant and wild type embryos were treated similarly.

A CLAHE filter was used to enhance the contrast of DAPI-stained embryos which were also imaged using the Prairie two-photon system (20x objective and laser tuned to 890 nm). Defined embryonic structures (e.g. neural tube) were then segmented by manual contouring and 3D rendered using Amira (Thermo-Fisher Scientific).

To analyse the LuVeLu time-series, we concatenated all 3D datasets and converted to a 4D dataset in HDF5 format. The time-points were then registered using the BigStitcher plugin (Hörl et al., 2019). Visualization and analysis were done using Imaris.

Data availability

Sequencing data have been deposited in GEO under accession code GSE147100.

The following data sets were generated
    1. Dias A
    2. Mallo M
    (2020) NCBI Gene Expression Omnibus
    ID GSE147100. Single-cell RNA sequencing of neuromesodermal progenitors of early headfold wild type embryos.
    https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE147100
The following previously published data sets were used
    1. Aires R
    2. Mallo M
    (2018) NCBI Sequence Read Archive
    ID SRX4968732. RNA-Seq of mus musculus: Tailbud WT1.
    https://www.ncbi.nlm.nih.gov/sra/SRX4968732
    1. Aires R
    2. Mallo M
    (2018) NCBI Sequence Read Archive
    ID SRX4968731. RNA-Seq of mus musculus: Tailbud WT2.
    https://www.ncbi.nlm.nih.gov/sra/SRX4968731
    1. deLemos L
    2. Mallo M
    (2019) NCBI Sequence Read Archive
    ID SRX5532193. RNA-seq of mus musculus : Tail Bud progenitors 2.
    https://www.ncbi.nlm.nih.gov/sra/SRX5532193
    1. deLemos L
    2. Mallo M
    (2019) NCBI Sequence Read Archive
    ID SRX5532192. RNA-seq of mus musculus : Tail Bud progenitors 1.
    https://www.ncbi.nlm.nih.gov/sra/SRX5532192
    1. Wymeersch FJ
    2. Skylaki S
    3. Huang Y
    4. Watson JA
    5. Economou C
    6. Marek-Johnston C
    7. Tomlinson SR
    8. Wilson V
    (2018) NCBI Gene Expression Omnibus
    ID GSE120870. Gene expression in microdissected embryonic regions during mouse axis elongation.
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Article and author information

Author details

  1. André Dias

    Instituto Gulbenkian de Ciência, Oeiras, Portugal
    Contribution
    Conceptualization, Formal analysis, Investigation, Writing - review and editing
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3337-6373

  2. Anastasiia Lozovska

    Instituto Gulbenkian de Ciência, Oeiras, Portugal
    Contribution
    Investigation
    Contributed equally with
    Filip J Wymeersch
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-9842-6450

  3. Filip J Wymeersch

    Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh, United Kingdom
    Present address
    RIKEN Center for Biosystems Dynamics Research, Hyogo, Japan
    Contribution
    Investigation, Methodology
    Contributed equally with
    Anastasiia Lozovska
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0001-8999-4555

  4. Ana Nóvoa

    Instituto Gulbenkian de Ciência, Oeiras, Portugal
    Contribution
    Investigation
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-5668-5630

  5. Anahi Binagui-Casas

    Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh, United Kingdom
    Contribution
    Investigation, Methodology
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-7987-9286

  6. Daniel Sobral

    Instituto Gulbenkian de Ciência, Oeiras, Portugal
    Present address
    UCIBIO, Departamento de Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, Caparica, Portugal
    Contribution
    Formal analysis, Methodology
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3955-0117

  7. Gabriel G Martins

    1. Instituto Gulbenkian de Ciência, Oeiras, Portugal
    2. Faculdade de Ciências da Universidade de Lisboa, Lisboa, Portugal
    Contribution
    Data curation, Methodology
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-6506-9776

  8. Valerie Wilson

    Centre for Regenerative Medicine, Institute for Regeneration and Repair, University of Edinburgh, Edinburgh, United Kingdom
    Contribution
    Supervision, Funding acquisition, Methodology
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-4182-5159

  9. Moises Mallo

    Instituto Gulbenkian de Ciência, Oeiras, Portugal
    Contribution
    Conceptualization, Supervision, Funding acquisition, Investigation, Writing - original draft, Project administration, Writing - review and editing
    For correspondence
    mallo@igc.gulbenkian.pt
    Competing interests
    No competing interests declared
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-9744-0912

Funding

Fundação para a Ciência e a Tecnologia (PTDC/BEX-BID/0899/2014)

  • Moises Mallo

Fundação para a Ciência e a Tecnologia (LISBOA-01-0145-FEDER-030254)

  • Moises Mallo

Fundação para a Ciência e a Tecnologia (LISBOA-01-0145-FEDER-022170)

  • Moises Mallo

Fundação para a Ciência e a Tecnologia (PD/BD/128426/2017)

  • André Dias

Fundação para a Ciência e a Tecnologia (PD/BD/128437/2017)

  • Anastasiia Lozovska

Santa Casa da Misericórdia (SCML-MC-60-2014)

  • Moises Mallo

Medical Research Council (MR/S008799/1)

  • Valerie Wilson

Medical Research Council (MR/K011200/1)

  • Valerie Wilson

Company of Biologists (DEV-170806)

  • André Dias

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We would like to thank Achim Gossler for the T-Str enhancer, Olivier Pourquié and Alexander Aulehla for the LuVeLu reporter strain, Sólveig Thorsteinsdóttir for the laminin antibody, Angela Nieto for Snai1 cDNA, Julien Delile for sharing data files, Luisa de Lemos for sharing unpublished data, Daniel Neves for the help with the analysis of the RNA-seq data, Hugo Pereira for the help using BigStitcher and Nuno Granjeiro for helping to set up the live imaging apparatus. We also would like to thank the IGC and SCRM animal facilities, Fiona Rossi and Clair Cryer from the SCRM flow cytometry facility, João Sobral from the IGC genomics facility, and past and present members of the Mallo lab for useful comments and support during the course of this project. This work has been supported by grants PTDC/BEX-BID/0899/2014 and LISBOA-01–0145-FEDER-030254 (FCT, Portugal) and SCML-MC-60–2014 (Santa Casa da Misericórdia, Portugal) to M.M.; the research infrastructure Congento, project LISBOA-01–0145-FEDER-022170; PhD fellowships PD/BD/128426/2017 to AD and (PD/BD/128437/2017) to AL (FCT, Portugal); MRC (UK) grants MR/S008799/1 and MR/K011200/1 to V.W. and a Development Travelling Fellowship (DEV-170806) from ‘The Company of Biologists’ to AD.

Ethics

Animal experimentation: Experiments involving animals carried out in the Oeiras laboratory followed the Portuguese (Portaria 1005/92) and European (Directive 2010/63/EU) legislations, concerning housing, husbandry, and welfare. The project was reviewed and approved by the Ethics Committee of "Instituto Gulbenkian de Ciência" and by the Portuguese National Entity, "Direcção Geral de Alimentação Veterinária" (license reference: 014308).

Version history

  1. Received: March 3, 2020
  2. Accepted: June 18, 2020
  3. Version of Record published: June 29, 2020 (version 1)

Copyright

© 2020, Dias et al.

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

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  1. André Dias
  2. Anastasiia Lozovska
  3. Filip J Wymeersch
  4. Ana Nóvoa
  5. Anahi Binagui-Casas
  6. Daniel Sobral
  7. Gabriel G Martins
  8. Valerie Wilson
  9. Moises Mallo
(2020)
A Tgfbr1/Snai1-dependent developmental module at the core of vertebrate axial elongation
eLife 9:e56615.
https://doi.org/10.7554/eLife.56615

Share this article

https://doi.org/10.7554/eLife.56615

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