Plasticity in sensory signaling is partly mediated via regulated trafficking of signaling molecules to and from primary cilia. Tubby-related proteins regulate ciliary protein transport; however, their roles in remodeling cilia properties are not fully understood. We find that the C. elegans TUB-1 Tubby homolog regulates membrane morphogenesis and signaling protein transport in specialized sensory cilia. In particular, TUB-1 is essential for sensory signaling-dependent reshaping of olfactory cilia morphology. We show that compromised sensory signaling alters cilia membrane phosphoinositide composition via TUB-1-dependent trafficking of a PIP5 kinase. TUB-1 regulates localization of this lipid kinase at the cilia base in part via localization of the AP-2 adaptor complex subunit DPY-23. Our results describe new functions for Tubby proteins in the dynamic regulation of cilia membrane lipid composition, morphology, and signaling protein content, and suggest that this conserved family of proteins plays a critical role in mediating cilia structural and functional plasticity.https://doi.org/10.7554/eLife.48789.001
Primary cilia are sensory organelles that are specialized to detect and transduce external stimuli (Bangs and Anderson, 2017; Hilgendorf et al., 2016; May-Simera et al., 2017). Cilia contain a microtubule-based axoneme surrounded by a membrane that houses cell- and context-specific subsets of signal transduction molecules. The axoneme is built by the highly conserved process of intraflagellar transport (IFT) that traffics molecules such as tubulin and signaling proteins into and out of cilia via kinesin and dynein molecular motors (Goetz et al., 2009; Kozminski et al., 1993; Rosenbaum and Witman, 2002; Scholey, 2003; Taub and Liu, 2016). IFT mechanisms have been extensively studied across species, and both core and accessory IFT molecules have been identified and characterized (Cole et al., 1998; Scholey, 2003; Taschner and Lorentzen, 2016). However, the pathways necessary for cilia membrane biogenesis, and trafficking of ciliary signaling molecules, remain to be fully described.
Cilia membrane volume and signaling protein content is regulated dynamically both as a function of cell type and external stimuli (Doroquez et al., 2014; Falk et al., 2015; Goetz et al., 2009; Mesland et al., 1980; Mukhopadhyay et al., 2008; Mykytyn and Askwith, 2017; Silverman and Leroux, 2009). For instance, vertebrate photoreceptor outer segments are built and maintained by cell-specific membrane delivery and retrieval mechanisms (Goldberg et al., 2016; Molday and Moritz, 2015). In mammalian cells, Sonic Hedgehog (Shh) signaling regulates ciliary trafficking of the Smoothened and GPR161 G-protein-coupled receptors (GPCRs), as well as the Shh receptor Patched (Bangs and Anderson, 2017; Corbit et al., 2005; Huangfu et al., 2003; Mukhopadhyay et al., 2013; Rohatgi et al., 2007). Since there is no protein translation within cilia, bulk cilia membrane and associated proteins are delivered to the cilia base via vesicular trafficking prior to transport into cilia (Jensen and Leroux, 2017; Mukhopadhyay et al., 2017; Nachury and Mick, 2019). In one pathway, post-Golgi vesicles or recycling endosomes fuse to the membrane of a specialized domain at the cilium base referred to as the ciliary pocket or periciliary membrane compartment (PCMC) (Benmerah, 2013; Ghossoub et al., 2011; Kaplan et al., 2012). Vesicle fusion is followed by lateral diffusion, or more commonly IFT-mediated trafficking, of these proteins into the cilia membrane (Badgandi et al., 2017; Fu et al., 2016; Hirano et al., 2017; Milenkovic et al., 2009; Mukhopadhyay et al., 2010; Picariello et al., 2019). Removal of ciliary membrane proteins is mediated via ectocytosis from the cilia tip, endocytosis at the cilia base, or lateral diffusion (Besharse et al., 1977; Clement et al., 2013; Lechtreck et al., 2009; Nager et al., 2017; Pal et al., 2016; Ye et al., 2018). Cilia membrane delivery and retrieval mechanisms are tightly controlled to ensure effective and efficient signal transduction.
Members of the conserved family of Tubby (TUB) and Tubby-like (TULP) proteins link vesicular trafficking at the cilia base with IFT-mediated trafficking of membrane proteins within cilia (Mukhopadhyay and Jackson, 2011; Wang et al., 2018). TULP1 is expressed specifically in photoreceptors and regulates vesicular transport of phototransduction molecules in the inner segment, but does not travel into the photoreceptor cilium itself (Hagstrom et al., 2001; Hagstrom et al., 1999; Milam et al., 2000; North et al., 1997). In contrast, the more broadly expressed TULP3 and TUB proteins transport GPCRs and channels into cilia via interactions with the IFT-A complex (Badgandi et al., 2017; Loktev and Jackson, 2013; Mukhopadhyay et al., 2010; Sun et al., 2012). Similarly, the Tubby homologs dTULP in Drosophila melanogaster and TUB-1 in Caenorhabditis elegans mediate ciliary trafficking of channels and GPCRs in ciliated sensory neurons (Brear et al., 2014; Mak and Ruvkun, 2004; Mukhopadhyay et al., 2005; Park et al., 2013). Thus, TUB/TULP proteins represent excellent targets of regulatory pathways that dynamically modulate ciliary membrane protein trafficking.
All TUB/TULP proteins directly bind phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2] via their conserved C-terminal Tubby domains (Santagata et al., 2001). Binding of this phosphoinositide facilitates interaction of TUB/TULP proteins with ciliary transmembrane proteins in the PCMC/ciliary pocket and subsequent transport via the IFT-A complex into cilia (Badgandi et al., 2017; Mukhopadhyay et al., 2010). The PCMC membrane is enriched in PI(4,5)P2, consistent with a requirement of this lipid for exo- and endocytosis (De Craene et al., 2017; Martin, 2012; Martin, 2015; Posor et al., 2015). However, PI(4,5)P2 is depleted from the cilia membrane due to the presence of the phosphoinositide 5-phosphatase INPP5e within cilia (Chávez et al., 2015; Garcia-Gonzalo et al., 2015; Jensen et al., 2015; Park et al., 2015). Absence of PI(4,5)P2 in the cilia membrane is proposed to weaken interaction of TUB/TULP proteins with their cargo and promote cargo release (Badgandi et al., 2017). Consequently, precise regulation of membrane phosphoinositide composition is critical for cilia membrane morphogenesis and membrane protein trafficking. Whether modulation of cilia and PCMC membrane phosphoinositide composition underlies plasticity in cilia protein content is unknown.
As in other animals, cell-specific sets of signal transduction molecules are trafficked and localized to the cilia of the 12 sensory neuron pairs present in the bilateral amphid sense organs in the head of the C. elegans hermaphrodite (Nguyen et al., 2014; Roayaie et al., 1998; Tobin et al., 2002; Troemel et al., 1995; Wojtyniak et al., 2013). A notable feature of these sensory cilia is their diverse morphologies. Eight of the 12 sensory neuron pairs contain one or two rod-like cilia (‘channel’ cilia), whereas the AWA, AWB, and AWC sensory neurons contain cilia (‘wing’ cilia) with unique axonemal ultrastructures and specialized membrane morphologies (Doroquez et al., 2014; Perkins et al., 1986; Ward et al., 1975). The membrane morphologies of the wing but not channel cilia are subject to further remodeling based on sensory inputs (Mukhopadhyay et al., 2008). The mechanisms that regulate cilia membrane biogenesis during development, and dynamic remodeling in response to sensory signaling in the adult, are not fully characterized.
Here, we show that the C. elegans TUB-1 Tubby homolog is required for the biogenesis of specialized membrane morphologies in wing cilia. TUB-1 is also necessary for sensory signaling-dependent expansion of the membrane in AWB wing cilia. Intriguingly, compromised sensory signaling results in increased levels of PI(4,5)P2 as well as TUB-1 within AWB cilia, suggesting that ciliary membrane phosphoinositide composition can be dynamically altered in response to sensory inputs. This altered ciliary phospholipid composition is mediated via TUB-1-dependent ciliary localization of the type I phosphatidylinositol-4-phosphate 5-kinase (PIP5K) PPK-1. We further show that TUB-1 regulates PPK-1 and PI(4,5)P2 distribution in AWB dendrites in part via localization of the DPY-23 AP-2 μ2 subunit of the clathrin adaptor complex at the PCMC. Our results identify the conserved TUB-1 Tubby protein as a key regulator of membrane biogenesis in specialized cilia, demonstrate that cilia membrane phosphoinositide composition is subject to dynamic modulation as a function of sensory input, and describe a new function for TUB-1 in regulating cilia membrane lipid and protein content via regulated trafficking of a lipid kinase.
To characterize potential ciliary functions of TUB-1, we surveyed the morphologies of individual amphid sensory neuron cilia in tub-1 mutant adult hermaphrodites. Wild-type AWA cilia are complex and highly branched, whereas AWC cilia exhibit large wing-like structures (‘fans’) comprised of a flattened membrane surrounding splayed out axonemal microtubules (Doroquez et al., 2014; Evans et al., 2006; Perkins et al., 1986) (Figure 1A). Each AWB neuron has two cilia, containing short proximal axonemes and distal membraneous regions with few disorganized microtubules (Figure 1A) (Doroquez et al., 2014; Mukhopadhyay et al., 2008). AWA cilia complexity was reduced in tub-1 mutants; we also observed branches emanating from the AWA PCMC in these animals (Figure 1A). The extent of the membraneous ciliary fans was markedly decreased in AWC, and AWB cilia were severely truncated, in tub-1 mutants (Figure 1A–B). The mutant AWB cilia morphology phenotype was fully rescued upon expression of wild-type tub-1, but not human TULP1 or TULP3, sequences specifically in AWB (Figure 1B, Figure 1—figure supplement 1). These observations indicate that TUB-1 acts in a cell-specific manner to shape specialized wing cilia morphology.
The phenotypes of AWB and AWC cilia suggested that the membraneous expansions in these cilia are reduced or lost in tub-1 mutants. To test this notion, we labeled the AWB cilia membrane and the axoneme via co-expression of a myristoylated tagRFP reporter and the GFP-tagged OSM-6 IFT-B component, respectively. As reported previously, OSM-6::GFP was largely restricted to a short proximal segment corresponding to the region containing the organized axoneme (Mukhopadhyay et al., 2007b), whereas membrane-associated myr-tagRFP was present throughout the AWB cilia in wild-type animals (Figure 1C). The distal myr-tagRFP-labeled membraneous regions were lost in tub-1 mutants while OSM-6::GFP localization was unaltered (Figure 1C), indicating that the cilia membrane, but not axonemes, are affected upon loss of tub-1 in AWB cilia.
Loss of dTULP and TULP1 in Drosophila rhabdomeric and mammalian ciliary photoreceptors, respectively, leads to progressive retinal degeneration (Chen et al., 2012; Gu et al., 1998; Hagstrom et al., 1998). We asked whether AWB ciliary membrane is also progressively lost in tub-1 mutants. Ciliogenesis is initiated following amphid sensory neuron birth late in embryogenesis in C. elegans (Nechipurenko et al., 2017; Serwas et al., 2017). Interestingly, the lengths of AWB cilia in L1 larvae were similar in wild-type and tub-1(nr2004) animals (Figure 1B). However, while wild-type AWB cilia elongated through postembryonic stages into adulthood, AWB cilia lengths in tub-1 mutants were not further altered (Figure 1B). We infer that TUB-1 is required to extend the distal membraneous regions of AWB cilia during postembryonic development.
Unlike in wing cilia, axonemes span the lengths of channel cilia (Doroquez et al., 2014; Perkins et al., 1986; Ward et al., 1975) (Figure 1D). Consistent with the notion that TUB-1 does not regulate axoneme elongation, the lengths of the single rod-like channel cilia of the ASK sensory neurons were unaltered in tub-1 mutants, whereas the lengths of the ASH and ASI neuronal cilia were only slightly, albeit significantly, shortened in these animals (Figure 1D–E) (Brear et al., 2014). Knockout of TULP3 has also been recently reported to result in a slight but significant shortening of primary cilia in mammalian cells (Han et al., 2019). Together, these observations indicate that TUB-1 is necessary for elaboration of the cilia membrane in a subset of amphid sensory neurons in C. elegans.
Loss of cilia membrane is expected to be associated with defects in the localization of ciliary transmembrane proteins. We previously showed that TUB-1 is required for localization of ciliary GPCRs in AWB (Brear et al., 2014). In tub-1 mutants, all previously examined GPCR::GFP fusion proteins are depleted from AWB cilia and are instead enriched at the PCMC (Kaplan et al., 2012). Although localization of a subset of GPCRs is also TUB-1-dependent in ASK, ciliary localization of the SRBC-64 GPCR is TUB-1-independent in this neuron type (Brear et al., 2014). To ask whether TUB-1 acts in a neuron- or GPCR-specific manner to localize SRBC-64, we examined whether SRBC-64 localization in AWB requires TUB-1. We found that SRBC-64::GFP was mislocalized to the PCMC in tub-1 mutants (Figure 2A), similar to the localization defects of other examined GPCRs. These observations imply that TUB-1 is required to correctly traffic and/or localize multiple GPCRs to AWB cilia.
In addition to GPCRs, Tubby family proteins traffic multiple classes of ciliary transmembrane proteins in ciliated mammalian cells and Drosophila sensory neurons (Badgandi et al., 2017; Grossman et al., 2011; Park et al., 2013; Park et al., 2015). In C. elegans, the ciliary localization of the cyclic nucleotide-gated channel protein TAX-4 was also TUB-1-dependent in AWB, such that this protein was depleted from cilia and mislocalized to the PCMC in tub-1 mutants (Figure 2B). The protein mislocalization phenotype in AWB is unlikely to simply be a secondary consequence of shortened cilia since TAX-4 localization was unaltered in odr-3(gof) Gα mutants in which AWB cilia are also severely shortened (Figure 2—figure supplement 1) (Mukhopadhyay et al., 2008). Recently, TULP3 was shown to regulate localization of the small GTPase ARL13b in mammalian cilia (Han et al., 2019; Hwang et al., 2019; Legué and Liem, 2019). In C. elegans, ARL-13 is also restricted to cilia, and regulates ciliary localization of multiple classes of transmembrane proteins (Cevik et al., 2010; Li et al., 2010; Li et al., 2012; Nguyen et al., 2014; Wojtyniak et al., 2013). While ARL-13::tagRFP was restricted to AWB cilia in wild-type animals, this fusion protein was also present at the AWB PCMC and distal dendritic regions in tub-1 mutants (Figure 2C). Localization of the DYF-19 basal body and MKS-5 transition zone proteins (Wei et al., 2013; Williams et al., 2011) was unaltered in the AWB cilia of tub-1 mutants (Figure 2D–E), suggesting that mislocalization of transmembrane and membrane-associated proteins in tub-1 mutants was likely not due to gross defects in transition zone organization.
Since TUB-1 is also required to localize a subset of GPCRs in ASK channel cilia (Brear et al., 2014) despite playing only a minor role in regulating channel cilia length, we examined the localization of additional ciliary proteins in channel cilia in tub-1 mutants. The TAX-2::GFP channel subunit was mislocalized to the distal dendritic ends of ASK in tub-1 mutants, similar to the mislocalization phenotype of TAX-4::GFP in AWB (Figure 2F). However, in contrast to AWB, ARL-13::RFP localization was unaltered in tub-1 mutants in ASH cilia (Figure 2G). These data suggest that the role of TUB-1 in regulating ciliary trafficking and localization of transmembrane and membrane-associated proteins in AWB and channel cilia are likely distinct.
To begin exploring the mechanisms by which TUB-1 regulates wing cilia membrane morphogenesis, we examined its subcellular localization in AWB. TUB-1 has been reported to be cytoplasmic and present throughout the cell including within the cilia of sensory neurons in C. elegans (Mak et al., 2006; Mukhopadhyay et al., 2005). Consistent with these observations, a functional tagRFP::TUB-1 fusion protein (Figure 1B) was present in the cytoplasm and excluded from the nucleus in AWB (Figure 3A). We noted marked enrichment of the protein at the PCMC with lower levels within the cilia proper (Figure 3A).
Tubby-like proteins contain a divergent N-terminal domain (NTD) and a conserved C-terminal Tubby domain (Ikeda et al., 2002; Mukhopadhyay and Jackson, 2011; Wang et al., 2018) (Figure 3B). Interaction of TULP3/TUB with diverse ciliary localization sequences present on ciliary transmembrane proteins is facilitated by binding of PI(4,5)P2 via a pair of conserved positively charged residues in the Tubby domain (Figure 3B) (Badgandi et al., 2017; Mukhopadhyay et al., 2010; Quinn et al., 2008; Santagata et al., 2001). Residues in the NTDs of TULP3 and TUB interact with IFT-A complex proteins (Figure 3B) that in turn traffic the TULP3/TUB-associated transmembrane protein complex into cilia (Badgandi et al., 2017; Mukhopadhyay et al., 2010). Thus, both the NTD and Tubby domains are required for ciliary trafficking functions of TULP3/TUB in mammalian cells (Badgandi et al., 2017; Mukhopadhyay et al., 2010; Park et al., 2013).
Consistent with trafficking into the cilium being mediated by residues in the TUB-1 NTD, we found that the TUB-1 Tubby domain alone [tagRFP::TUB-1(CTD)] was excluded from AWB cilia and restricted to an expanded domain at the cilia base (Figure 3C, Figure 3E). In contrast, a fusion protein containing the NTD alone [tagRFP::TUB-1(NTD)] and lacking the PI(4,5)P2-binding Tubby domain was no longer enriched at the PCMC and was present uniformly in the AWB dendrites and cilia (Figure 3C, Figure 3E). Expression of neither fusion protein alone was sufficient to rescue the AWB cilia phenotype of tub-1 mutants (Figure 3F). These observations imply that TUB-1 functions at both the PCMC and within cilia to shape AWB cilia morphology.
We next characterized the residues within the NTD and Tubby domains that mediate TUB-1 localization to distinct regions in AWB. Residues in the NTDs of TULP3 and TUB that mediate interaction with IFT-A complex proteins were predicted to be absent in TUB-1 (Mukhopadhyay and Jackson, 2011). However, upon closer examination of the TUB-1 NTD sequence, we identified a subset of conserved residues in the homologous IFT-A binding domain (Figure 3B). Mutations in these residues resulted in depletion of the mutant protein [tagRFP::TUB-1(QRKRmut)] from cilia and localization to an expanded domain at the AWB ciliary base and distal dendritic region (Figure 3C, Figure 3E). This fusion protein also failed to rescue the AWB ciliary morphology defects of tub-1 mutants (Figure 3F). Consistent with the notion that TUB-1 is trafficked via IFT into the AWB cilia, both tub-1 and daf-10 IFT122 IFT-A mutants exhibit similar phenotypes of ciliary GPCR accumulation at the AWB PCMC (Brear et al., 2014), and resulted in similar AWB cilia truncation phenotypes (Figure 3—figure supplement 1A). Localization of DAF-10 was unaltered in the AWB cilia of tub-1 mutants (Figure 3—figure supplement 1B). However, while mutations in the kap-1 kinesin II subunit required for IFT did not affect ciliary TUB-1 localization, we observed increased accumulation of TUB-1 at the PCMC (Figure 3D), further suggesting that TUB-1 is trafficked into cilia via IFT.
Mutating the predicted PI(4,5)P2-binding residues (Figure 3B) in the Tubby domain of TUB-1 [tagRFP::TUB-1(KRmut)] resulted in loss of PCMC enrichment similar to the localization pattern of tagRFP::TUB-1(NTD) (Figure 3C, Figure 3E), and abolished the ability of this protein to rescue the AWB cilia phenotype of tub-1 mutants (Figure 3F). Although Tubby proteins have also been reported to localize to the nucleus under specific conditions (Boggon et al., 1999; He et al., 2000; Kim et al., 2017; Park et al., 2013; Santagata et al., 2001), we did not detect nuclear localization of full-length TUB-1, TUB-1(NTD) or TUB-1(KRmut) fusion proteins (Figure 3A, Figure 3—figure supplement 1C). We infer that TUB-1 is trafficked into cilia via interaction of its NTD with the IFT machinery, whereas enrichment of TUB-1 at the AWB PCMC requires interaction with PI(4,5)P2 via its Tubby domain.
We previously showed that under conditions of reduced or absent sensory signaling, the ciliary membrane in AWB is significantly expanded resulting in a membraneous fan-like shape (Mukhopadhyay et al., 2008). Given a role for TUB-1 in regulating AWB cilia membrane morphogenesis during development, we tested whether TUB-1 is necessary for sensory signaling-dependent remodeling of AWB cilia.
As reported previously (Mukhopadhyay et al., 2008), AWB cilia width is significantly increased in odr-1 receptor guanylyl cyclase signaling mutants (Figure 4A). This sensory signaling-dependent ciliary membrane expansion was fully suppressed upon loss of tub-1 (Figure 4A). Loss-of-function mutations in daf-10 also suppressed the expanded fan phenotype of odr-1 mutants (Figure 4—figure supplement 1). The subcellular localization of Tubby proteins can be altered by cellular signaling (Chen et al., 2012; Kim et al., 2014; Santagata et al., 2001); we asked whether the expanded fan-like structure in odr-1 mutants is accompanied by increased ciliary TUB-1 levels. Indeed, we found that odr-1 mutants showed enrichment of a TUB-1 fusion protein in AWB cilia as compared to levels at the PCMC (Figure 4B). These results raise the possibility that reduced sensory signaling in odr-1 mutants requires increased ciliary localization of TUB-1 to modulate ciliary membrane expansion. However, it remains possible that the severely truncated cilia in tub-1 and daf-10 mutants are unable to elaborate fans.
While TUB-1 has previously been suggested to undergo IFT in C. elegans sensory cilia (Mukhopadhyay et al., 2005), we were unable to perform live imaging of TUB-1 movement in wild-type AWB cilia due to low ciliary expression levels of this protein (Figure 3A) and the occurrence of IFT primarily in the short proximal region containing the axoneme (Mukhopadhyay et al., 2007b). To examine TUB-1 ciliary dynamics, we instead quantified recovery of GFP::TUB-1 fluorescence in the AWB cilia of wild-type and odr-1 mutants following photobleaching (FRAP). We found that while fluorescence recovery occurred at a similar rate in wild-type and odr-1 mutants, a significantly higher fraction of the TUB-1 fusion protein was mobile in the AWB cilia of odr-1 mutants as compared to wild-type animals (Figure 4C–E). These results further support the notion that decreased sensory signaling in odr-1 mutants increases trafficking of TUB-1 within AWB cilia.
The increased presence of TUB-1 in the AWB cilia of odr-1 mutants is reminiscent of phenotypes observed upon manipulation of ciliary membrane PI(4,5)P2 levels. PI(4,5)P2 is excluded from the cilia membrane in both vertebrates and Drosophila, primarily due to ciliary localization of the phosphatases such as INPP5e which converts PI(4,5)P2 to PI(4)P (Bielas et al., 2009; Chávez et al., 2015; Garcia-Gonzalo et al., 2015; Jacoby et al., 2009; Park et al., 2015; Prosseda et al., 2017). Since TULP3/TUB proteins interact directly with PI(4,5)P2, absence of ciliary PI(4,5)P2 is associated with low levels of these proteins in wild-type cilia. However, upon depletion of INPP5e, increased ciliary PI(4,5)P2 markedly enhances ciliary levels of TULP/TUB proteins (Chávez et al., 2015; Garcia-Gonzalo et al., 2015; Park et al., 2015). We asked whether increased ciliary localization of TUB-1 in odr-1 mutants is associated with changes in ciliary membrane PI(4,5)P2 distribution.
We first examined PI(4,5)P2 distribution in wild-type AWB cilia using a GFP::PLCδ1-PH fusion protein (Jensen et al., 2015). Similar to observations in other organisms, C. elegans sensory cilia membranes are depleted in PI(4,5)P2, although individual sensory cilia have not been examined (Jensen et al., 2015). We confirmed that GFP::PLCδ1-PH was associated with the dendritic and PCMC, but not the ciliary, membranes of AWB (Figure 5A–B, also see Figure 6D–F). In AWB dendrites, we observed that GFP::PLCδ1-PH exhibited maximal fluorescence intensity ~2–3 μm proximally from the cilia base (Figure 5A, also see Figure 6D–E).
We tested whether increasing ciliary PI(4,5)P2 levels is sufficient to increase ciliary localization of TUB-1. The CIL-1 and INPP-1 phosphatases are the closest homologs of INPP5e in C. elegans (Bae et al., 2009). CIL-1 does not appear to regulate PI(4,5)P2 levels (Bae et al., 2009). However, in inpp-1 mutants, PLCδ1-PH was now also present in AWB cilia (Figure 5A–B). Consistent with the preferential association of TUB-1 with PI(4,5)P2, we also observed higher levels of tagRFP::TUB-1 in AWB cilia in inpp-1 mutants; this altered localization phenotype was rescued upon expression of a wild-type inpp-1 cDNA (Figure 5C). We next asked whether similar to inpp-1 mutants, ciliary PI(4,5)P2 levels are also increased in odr-1 mutants to account for the increased ciliary localization of TUB-1. Indeed, we found that the AWB cilia membrane contained higher levels of PI(4,5)P2 relative to dendritic concentrations in odr-1 mutants as compared to the ratio in wild-type animals (Figure 5A–B, also see Figure 6D, Figure 6F). We conclude that compromised sensory signaling in odr-1 mutants is associated with increased ciliary PI(4,5)P2 distribution, which in turn is correlated with increased ciliary TUB-1 localization. However, since AWB cilia did not exhibit a fan-like phenotype in inpp-1 mutants (Figure 5A), increased ciliary PI(4,5)P2 and TUB-1 levels are not sufficient to remodel AWB cilia morphology (see Discussion).
How might reduced sensory signaling increase ciliary PI(4,5)P2? Reduced sensory signaling could result in depletion of ciliary INPP-1 and/or increased ciliary localization of a PIP5K that generates PI(4,5)P2 from PI(4)P. Unlike in mammalian cells or in Drosophila (Chávez et al., 2015; Garcia-Gonzalo et al., 2015; Park et al., 2015), a functional INPP-1::GFP fusion protein (Figure 5C) was present at similar levels throughout the dendrites and cilia of wild-type AWB neurons (Figure 5—figure supplement 1). Localization of this fusion protein was unaltered in odr-1 or tub-1 mutants (Figure 5—figure supplement 1). We, therefore, considered it unlikely that differential localization of INPP-1 accounts for PI(4,5)P2 distribution in wild-type or odr-1 mutant AWB cilia, although we cannot rule out the presence of additional PI(4,5)P2 5-phosphatases or spatially restricted modulation of INPP-1 activity (Coon et al., 2012; Luo et al., 2012).
C. elegans encodes a single type I PIP5K homolog that is highly expressed in the nervous system (Weinkove et al., 2008; Xu et al., 2016; Xu et al., 2007). In AWB, a GFP::PPK-1 fusion protein injected at a low concentration was membrane-associated and exhibited a localization pattern that was similar to that of GFP::PLCδ1-PH (Figure 5D–E, also see Figure 6A). This fusion protein was absent in all examined AWB cilia and also exhibited maximal fluorescence intensity in a region approximately 2–3 μm proximal from the cilia base (Figure 5D–E, also see Figure 6A–B). In odr-1 mutants, we observed significantly increased relative levels of GFP::PPK-1 in AWB cilia (Figure 5D–E, also see Figure 6A, Figure 6C). We conclude that in odr-1 mutants, increased ciliary localization of PPK-1 contributes in part to increased ciliary levels of PI(4,5)P2.
We next investigated the mechanisms by which PPK-1 distribution in the AWB dendrites and cilia is regulated in wild-type and odr-1 mutant animals. Unexpectedly, we identified a role for TUB-1 in regulating PPK-1 localization. As shown in Figure 6A–B, as compared to PPK-1 distribution in wild-type animals, the majority of tub-1 mutant animals exhibited a proximal shift in GFP::PPK-1 localization with maximal enrichment starting at >4 μm from the cilia base in AWB dendrites (Figure 6A–B). Consistent with the observed change in GFP::PPK-1 distribution, GFP::PLCδ1-PH distribution in the AWB dendritic membrane was also altered upon loss of tub-1. In tub-1 mutants, localization of this fusion protein shifted proximally in the AWB dendrites with maximal fluorescence intensity at >4 μm from the cilia base (Figure 6D–E). This phenotype was partially rescued upon expression of full-length TUB-1 protein in AWB (Figure 6—figure supplement 1). We conclude that TUB-1 itself regulates dendritic phosphoinositide composition by regulating localization of PPK-1 in AWB.
If TUB-1-mediated ciliary localization of PPK-1 is necessary for sensory signaling-dependent redistribution of PI(4,5)P2, we would expect that loss of tub-1 would suppress the altered ciliary phosphoinositide phenotype of odr-1 mutants. Consistent with this notion, we found that loss of tub-1 significantly suppressed the increased ciliary PI(4,5)P2 localization phenotype of odr-1 mutants (Figure 6D, Figure 6F). Similarly, GFP::PPK-1 was no longer found in the cilia of tub-1; odr-1 double mutants (Figure 6A, Figure 6C). However, the dendritic localization patterns of the PI(4,5)P2 sensor and GFP::PPK-1 in AWB in tub-1; odr-1 double mutants were not identical to those of tub-1 single mutants alone. Few animals exhibited the proximal dendritic shift of GFP::PLCδ1-PH or GFP::PPK-1 localization observed in tub-1 single mutants. Instead, both proteins were shifted towards the ciliary base, although excluded from the AWB cilia proper, in tub-1; odr-1 double mutants (Figure 6). We interpret these results to suggest that TUB-1 is necessary to localize PPK-1 within AWB cilia in odr-1 mutants, but that an alternative mechanism partly compensates for loss of TUB-1 to localize PPK-1 to the ciliary base in tub-1; odr-1 double mutants.
Given the distinct roles of TUB-1 in wing and channel cilia, we asked whether TUB-1 also regulates ciliary PI(4,5)P2 distribution in ASK. As in AWB, TUB-1 was enriched at the PCMC of wild-type ASK (Figure 6—figure supplement 2A). Moreover, similar to observations in AWB, both GFP::PLCδ1-PH and GFP::PPK-1 were excluded from ASK cilia and exhibited maximal fluorescence at a distance of >3 μm from the cilia base in wild-type animals (Figure 6—figure supplement 2B–C). We observed no changes in the distribution pattern of either protein in tub-1 mutants (Figure 6—figure supplement 2B–C). We conclude that TUB-1 regulates localization of PPK-1 and PI(4,5)P2 specifically in AWB but not in ASK.
We next asked how TUB-1 might regulate PPK-1 and PI(4,5)P2 distribution in AWB dendrites. PIP5Ks are recruited to specific membrane subdomains via multiple mechanisms including direct interaction with AP-2 μ2 subunits (Krauss et al., 2006; Ling et al., 2007; Nakano-Kobayashi et al., 2007; Padrón et al., 2003). Tubby family proteins including C. elegans TUB-1 have previously been implicated in the regulation of endocytosis in multiple cellular contexts (Chen et al., 2012; Mukhopadhyay et al., 2007a; Wahl et al., 2016). Moreover, TUB interacts directly with Dynamin (Xi et al., 2007). We asked whether TUB-1 might regulate PPK-1 recruitment at the AWB PCMC in part via regulation of endocytic protein localization.
In wild-type animals, a DPY-23::GFP AP-2 μ2 subunit fusion protein was enriched at the PCMC of AWB in a domain similar to that occupied by TUB-1 (Kaplan et al., 2012) (Figure 7A). Levels of this fusion protein at the PCMC were significantly decreased although not abolished in tub-1 mutants in AWB (Figure 7A). If DPY-23 plays a role in recruiting PPK-1, we would expect PPK-1 and PI(4,5)P2 distribution in AWB to be affected in dpy-23 mutants. Although we were unable to examine the distribution of GFP::PPK-1 due to technical reasons, the distribution pattern of GFP::PLCδ1-PH was shifted proximally in the AWB dendrite in dpy-23 mutants, in a pattern similar but not identical to the distribution observed in tub-1 mutants (Figure 7B). We observed no changes in the localization of a DYN-1::GFP dynamin fusion protein at the AWB PCMC in tub-1 mutants (Figure 7—figure supplement 1A). A role for TUB-1 in regulating DPY-23 localization was specific for AWB, since localization of both DPY-23 and DYN-1 at the ASK PCMC was unaffected in tub-1 mutants (Figure 7—figure supplement 1B–C). We conclude that disrupted localization of DPY-23 in tub-1 mutants may in part contribute to the altered PPK-1 and PI(4,5)P2 distribution at the AWB PCMC.
Although tub-1 and dpy-23 mutants exhibit related defects in PI(4,5)P2 distribution in the AWB dendrite, their AWB cilia phenotypes are distinct. Unlike the truncated cilia phenotype of tub-1 mutants, endocytic mutants exhibit expanded ciliary membraneous fans in AWB similar to the phenotypes of sensory signaling mutants (Kaplan et al., 2012) (Figure 7C). As in odr-1 mutants, loss of tub-1 fully suppressed the expanded ciliary membrane phenotype of dpy-23 mutants (Figure 7C); AWB cilia lengths in tub-1; dpy-23 mutants were similar to those in tub-1 mutants alone (Figure 7C). However, in contrast to observations in odr-1 animals in which ciliary TUB-1 levels are increased, we observed no changes in ciliary concentrations of tagRFP::TUB-1 in dpy-23 mutants (Figure 7D). Instead, this fusion protein occupied a larger area at the ciliary base in dpy-23 animals (Figure 7D), similar to the mislocalization phenotype of a subset of ciliary IFT and transmembrane proteins in endocytic mutants (Kaplan et al., 2012). These observations imply that while TUB-1 is necessary for elaboration of the AWB ciliary membrane in wild-type, odr-1, and dpy-23 mutants, the phosphoinositide and protein content of these fan-like structures are distinct in these mutant backgrounds.
We show here that the TUB-1 Tubby protein acts both at the PCMC and within cilia to regulate ciliary membrane morphogenesis, and ciliary and dendritic membrane phosphoinositide composition, in part via localization of the PPK-1 lipid kinase (Figure 8). Under normal growth conditions, TUB-1 excludes PPK-1, and thus PI(4,5)P2, from cilia and regulates their distribution in AWB dendrites. This distribution may play an important role in regulating the correct balance between exocytosis and endocytosis at the PCMC, and trafficking of membrane proteins into cilia. In the absence of TUB-1, ciliary membrane proteins are mislocalized to the PCMC and the membraneous expansions of wing cilia are lost. TUB-1 is also necessary for sensory signaling-dependent remodeling of AWB cilia in odr-1 mutants. In odr-1 mutant animals, TUB-1 traffics PPK-1 into AWB cilia, thereby altering ciliary membrane phosphoinositide composition (Figure 8). Expanded cilia membrane volume together with increased ciliary signaling may represent a homeostatic mechanism that attempts to compensate for decreased sensory inputs in signaling mutants. We suggest that regulation of TUB-1-mediated transport represents a key mechanism underlying cell- and context-dependent ciliary morphological and functional diversification in a subset of C. elegans olfactory neurons.
How might TUB-1 regulate PPK-1 localization? The μ2 subunit of the AP-2 complex directly binds to and activates PIP5Ks (Krauss et al., 2006; Nakano-Kobayashi et al., 2007; Posor et al., 2015; Wallroth and Haucke, 2018). Localization of the DPY-23 AP-2 μ2 subunit at the AWB PCMC is decreased, although not abolished in tub-1 mutants, suggesting that TUB-1 recruits PPK-1 at the PCMC in part via DPY-23 (Figure 8). Consistent with this hypothesis, the pattern of PI(4,5)P2 distribution in AWB dendrites is similar in tub-1 and dpy-23 mutants. However, it is unlikely that TUB-1 acts via DPY-23 to increase PPK-1 levels within cilia in odr-1 mutants. The small G protein ARF6 also binds and activates PIP5Ks in multiple contexts (Funakoshi et al., 2011; Jones et al., 2000). Several small GTPases including ARL13b have been implicated in ciliogenesis and ciliary membrane morphogenesis (Blacque et al., 2018; Dilan et al., 2019; Li and Hu, 2011; Lu et al., 2015), and TULP3/TUB regulates ciliary localization of ARL13b (Han et al., 2019; Hwang et al., 2019; Legué and Liem, 2019) (this work). Given a specific role of TUB-1 in localizing ARL-13 to AWB but not channel cilia, we speculate that TUB-1 may act via a related small GTPase in a cell-specific manner to increase PPK-1 and PI(4,5)P2 levels in specialized cilia of sensory signaling mutants in C. elegans. However, it is also possible that disruption of transition zone architecture in odr-1 mutants enables ciliary access by PPK-1 (Garcia-Gonzalo et al., 2011; Jensen et al., 2015).
Altered PI(4,5)P2 distribution at the PCMC in tub-1 mutants is expected to significantly affect both endo- and exocytosis as well as entry and exit of ciliary proteins (Grossman et al., 2011; Martin, 2012; Park et al., 2015; Posor et al., 2015; Wallroth and Haucke, 2018). PI(4,5)P2 levels also alter multiple aspects of ciliogenesis including transition zone maturation (Gupta et al., 2018; Xu et al., 2016; Xu et al., 2019). However, since initial steps of ciliogenesis appear to be unaffected in tub-1 L1 larvae (see Figure 1B), we favor the hypothesis that TUB-1 regulates membrane biogenesis in AWB via regulation of vesicular trafficking at the cilia base and membrane transport within cilia. TUB-1 was previously suggested to target the RAB-7 small GTPase implicated in endocytic trafficking in C. elegans (Mukhopadhyay et al., 2007a), and Tubby proteins have similarly been implicated in the regulation of both exo- and endocytosis in multiple contexts including in cilia and photoreceptor ribbon synapses (Chen et al., 2012; Grossman et al., 2011; Hagstrom et al., 2001; Hagstrom et al., 1999; Park et al., 2013; Wahl et al., 2016). Our results raise the possibility that TULP1/dTULP modulates these processes via regulation of local PI(4,5)P2 pools.
The distribution and function of transmembrane signaling proteins is highly regulated by membrane lipids (Balla, 2013; Gamper and Shapiro, 2007; Hansen, 2015; Yen et al., 2018). Consistently, ciliary membrane lipid composition regulates targeting of ciliary transmembrane proteins including those required for Shh signaling, mechanotransduction, and phototransduction (Bae et al., 2009; Boesze-Battaglia and Schimmel, 1997; Chávez et al., 2015; Garcia-Gonzalo et al., 2015; Giusto et al., 2010; Park et al., 2015; Raleigh et al., 2018; Tyler et al., 2009). In C. elegans, under conditions of decreased sensory input as in odr-1 mutants, increasing ciliary surface to volume ratio together with alterations in ciliary PI(4,5)P2 levels may increase sensitivity to external stimuli. Do TULP/TUB proteins also regulate PI(4,5)P2 distribution within mammalian cilia? Although to our knowledge ciliary PI(4,5)P2 levels in TULP/TUB mutants have not been directly examined in mammalian cells, recent observations indicate that TULP3/TUB regulate ciliary enrichment of INPP5e via localization of ARL13b (Han et al., 2019; Humbert et al., 2012; Hwang et al., 2019; Legué and Liem, 2019). Based on the phenotype of inpp5e mutants, altered localization of INPP5e in TULP3/TUB mutants would be expected to increase ciliary membrane PI(4,5)P2 levels (Chávez et al., 2015; Garcia-Gonzalo et al., 2015; Park et al., 2015), suggesting a conserved role for Tubby proteins in regulating membrane phosphoinositide composition. These observations raise the intriguing possibility that dynamic TULP3/TUB-mediated ciliary transport of lipid-modification enzymes may represent a conserved mechanism that mediates plasticity in ciliary membrane protein composition and function in multiple contexts.
Although TUB-1 is necessary for membrane expansion in both odr-1 and dpy-23 mutants, increased ciliary localization of TUB-1 and/or PI(4,5)P2 is neither necessary nor sufficient for ciliary membrane expansion. The expanded AWB ciliary membrane in dpy-23 mutants does not contain increased TUB-1 or PI(4,5)P2, and increasing TUB-1 and PI(4,5)P2 within cilia does not lead to membrane expansion in inpp-1 mutants. In odr-1 mutants, increased TUB-1-mediated transport of membrane cargoes and PPK-1 to cilia may cause expansion of the ciliary membrane together with altered membrane phosphoinositide composition (Figure 8). In this model, while ciliary PI(4,5)P2 is also increased in inpp-1 mutants, TUB-1-mediated cargo delivery to cilia may not be enhanced similarly to odr-1 mutants, resulting in a failure to enlarge the cilia membrane. In endocytic mutants, while TUB-1 function at the PCMC and cilia continues to be necessary for membrane biogenesis, disruption of membrane retrieval mechanisms relative to membrane delivery results in AWB membrane volume remodeling (Kaplan et al., 2012). Regulation of ciliary membrane volume, lipid composition and protein content via multiple independent mechanisms may provide additional flexibility in reshaping cilia structure and function (Garcia et al., 2018; Lechtreck et al., 2013; Nachury, 2018; Phua et al., 2017). It will be particularly interesting to determine whether distinct mechanisms operate to modulate cilia morphology in different sensory signaling regimes.
Dynamic modulation of intracellular trafficking and cellular structures is a hallmark of cellular functional plasticity (Jin and Qi, 2018; Jontes and Smith, 2000; Nakahata and Yasuda, 2018; Sugie et al., 2018). This plasticity is particularly critical in neurons which must continuously modulate their properties in response to the animal’s experience and environment. Sensory cilia are subject to similar experience-dependent plasticity in their structures and signaling functions (Besschetnova et al., 2010; Caspary et al., 2007; Mesland et al., 1980; Mukhopadhyay et al., 2008); this work implicates the conserved TUB-1 protein in mediating this plasticity. An important open issue for the future will be to establish how sensory signals are interpreted and translated to alter TUB-1 properties in wing cilia, and the consequences of ciliary remodeling on neuronal functions.
Wild-type animals were C. elegans variety Bristol, strain N2. C. elegans strains were grown at 20°C on standard nematode growth media (NGM) plates seeded with the Escherichia coli strain OP50. Standard genetic techniques were used to introduce transgenes into mutant genetic backgrounds. Transgenic animals were generated by microinjection of test plasmid(s) at 0.5 ng–50 ng/μl of plasmid(s) together with a co-injection marker (unc-122p::gfp, unc-122p::mCherry, or unc-122p::dsRed) at 50 ng/μl. Mutations were confirmed by PCR and/or sequencing. Except where indicated, the same transgenic array was examined in both wild-type and mutant backgrounds. Animals from at least two independent lines were examined for each transgenic strain, and one representative line was typically chosen for further analysis. A complete list of all strains used in this work is provided in Supplementary file 1.
Constructs driving expression specifically in AWB were generated by fusing relevant cDNAs to 3.0 kb str-1 (Troemel et al., 1997) or the ~3.0 kb srd-23 (Colosimo et al., 2004) upstream regulatory sequences. Constructs driving expression specifically in ASK were generated by fusing relevant cDNAs to 1.9 kb srbc-64, 1.6 kb srbc-66 (Kim et al., 2009), or 2.9 kb sra-9 (Troemel et al., 1995) upstream regulatory sequences. The arl-13 cDNA was expressed in ASH under 3.8 kb sra-6 (Troemel et al., 1995) upstream regulatory sequences. tub-1, inpp-1 (isoform a), dyn-1 (isoform b), dpy-23 (isoform b), and ppk-1 cDNAs were amplified from a mixed stage N2 cDNA library using gene-specific primers. tax-2 and tax-4-expression constructs have been reported previously (Wojtyniak et al., 2013). The PLCδ1-PH-encoding cDNA was a gift from A. Rodal (Brandeis University). Human Tulp1 and Tulp3 cDNAs were a gift from S. Mukhopadhyay (UT Southwestern Medical Center). TUB-1 N- and C-terminal domain-encoding sequences were identified based on homology with Mus musculus Tubby sequences. All sequences were cloned into pPD95.77 (gift of A. Fire) or pMC10 (gift of M. Colosimo). N- and C-terminal reporter-tagged constructs were generated by subcloning fluorescent reporter sequences in-frame into expression vectors containing the gene of interest. In some cases, SL2::mScarlet coding sequences were also inserted to visualize neuron morphology. Point mutations in the tub-1 cDNA were generated using site-directed mutagenesis. All constructs were confirmed by sequencing. A full list of plasmids used in this work is provided in Supplementary file 2.
Except where indicated, all hermaphrodites were imaged as one day old adults, and one neuron per animal was examined. L1 larvae imaged in Figure 1B were obtained from growth synchronized adults, and imaged at 3–5 hr after hatch. All animals were mounted on 10% agarose pads set on microscope slides and immobilized using 10 mM tetramisole (Sigma). Unless noted otherwise, all imaging was performed on an inverted spinning disk confocal microscope (Zeiss Axiovert with a Yokogawa CSU22 spinning disk confocal head and a Photometerics Quantum SC 512 camera). Optical sections were acquired at 0.27 μm intervals using a 100X oil immersion objective and SlideBook 6.0 software (Intelligent Imaging Innovations, 3i). Images in Figure 4A were acquired at 0.25 μm intervals using a 63X oil immersion objective on an upright microscope (Zeiss Imager.M2 with a Hamamatsu C4742.95 camera) and were collected using Zeiss Zen software. Images in Figures 5D and 6A–C were acquired at 0.3 μm intervals using a 100X oil immersion objective on an upright spinning disk microscope (Nikon Ni-E with a Yokogawa CSU-W1 spinning disk head and an Andor iXon 897U EMCCD camera) and were collected using Nikon Elements AR software. Optical sections were z-projected at maximum intensity using SlideBook 6.0 software or FIJI/ImageJ [National Institutes of health (NIH), Bethesda, MD].
Fluorescence microscopy image processing and analyses were performed using FIJI. All quantifications were performed using data from a minimum of two and typically three biologically independent experiments performed on independent days. Methods used for specific analyses are described below.
Line segments were drawn from the cilia tip to the base and lengths of both AWB cilia per neuron were summed.
Cilium widths were quantified using line segments to identify the widest point of each AWB cilium, and the summed total was calculated.
Protein fluorescence intensities were quantified by outlining the cilia area in 2D maximum projected images and measuring the mean intensity. The average of three mean background intensities was subtracted from the mean intensity to arrive at the final value.
Fluorescence intensities in dendrites were quantified by outlining a 0.5 μm area region of the dendrite 5–8 μm from the cilia base and measuring the mean fluorescence intensity after background subtraction. DPY-23, DYN-1, or TUB-1 fusion protein fluorescence intensities at the cilia base were quantified by drawing a 1 μm diameter circular region of interest at the cilia base in the 2D maximum projected images and measuring the mean fluorescence intensity after background subtraction.
Protein fluorescence intensity ratios were analyzed in some instances to control for known expression differences driven by specific promoters such as str-1 and srd-23 in odr-1 mutants (van der Linden et al., 2007; van der Linden et al., 2008). Ratios were calculated by normalizing cilia protein fluorescence intensities by dendritic or base protein fluorescence intensities (calculated as described above).
To measure the length of TUB-1 enrichment at the cilia base, line segments were drawn from cilia base to the proximal end of the enrichment domain in the dendrite.
Line scans were generated by drawing lines from the ciliary base and along the dendrite, and measuring fluorescence intensities along the line using the plot profile tool in FIJI. Fluorescence intensities were normalized to the maximum intensity for each individual animal across the measured region, and the percent of this maximum intensity was quantified at each location to create individual line scans.
Animals were mounted on 10% agarose pads and immobilized using 10 mM tetramisole. Animals were imaged at 0.6 μm interval z-stacks using a 100X oil immersion objective on an upright spinning disk microscope (Nikon Ni-E with a Yokogawa CSU-W1 spinning disk head and an Andor iXon 897U EMCCD camera). Images were collected using Nikon Elements AR software. Cilia were photobleached using a 405 nm laser (at 40% power), directed by an Andor Mosaic three digital micromirror device. One or both AWB cilia were photobleached in wild-type and odr-1 mutants. Cilia were imaged at least 12 s prior to bleaching, and up to 2 min following the bleaching event at 3 s intervals to assess fluorescence recovery. Images were corrected for photobleaching using the Bleach Correction plugin and Simple Ratio Method in FIJI/Image J [National Institutes of health (NIH), Bethesda, MD]. Pre-bleach fluorescence was normalized to 100% in order to calculate the fraction of fluorescence recovery. The recovery half-times (t1/2) and mobility fractions (Mf) were calculated using Prism 6 Software (Graphpad, La Jolla, CA) by fitting individual recovery curves using one phase association nonlinear regression. The mean fluorescence recovery curves were created by plotting the mean and SEM of fluorescence intensities at individual time points after bleaching using Prism 6 Software (Graphpad, La Jolla, CA).
All plots were generated using Prism seven software. All scatterplots show mean ± SEM. Statistical significances among multiple strains were calculated using one-way ANOVA followed by Tukey’s multiple comparisons test. For comparisons between two groups, an unpaired student’s t test with equal SD was used.
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Oliver HobertReviewing Editor; Howard Hughes Medical Institute, Columbia University, United States
Anna AkhmanovaSenior Editor; Utrecht University, Netherlands
Maureen M BarrReviewer; Rutgers University, United States
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Congratulations, we are pleased to inform you that your article, "The C. elegans Tubby homolog dynamically modulates olfactory cilia membrane morphogenesis and phospholipid composition", has been accepted for publication in eLife.
As you will see, the reviewers were very impressed by the work described in the manuscript, including rigor and clarity. One reviewer had a comment that you can consider when uploading the final version of the manuscript.
The manuscript by DiTirro, Philbrook et al. examines the function of the Tubby homolog TUB-1 in ciliary membrane morphology of the C. elegans amphid wing AWB cilia. Authors convincing show that TUB-1 regulates morphology in a cell-type dependent manner (AWB but not ASK) and ciliary protein localization (TAX-4 and ARL-13 but not transition zone or IFT components). Next, they identify ciliary targeting determinants (IFT-A binding sites in the N-terminal domain). To link structure with function, authors show that tub-1 is required for sensory signaling ciliary membrane expansion (in odr-1 receptor guanylyl cyclase mutant). PIP2 and the PIP5K PPK-1 are normally excluded from AWB cilia but is present in the odr-1 mutant. From here, authors show that TUB-1 regulates PIP2 distribution via PPK-1 localization but not the localization of the INPP5e phosphatase INPP-1. Finally, authors connects PIP2 and the AP-2 μ2 endocytic adaptor DPY-23. The model for TUB-1 function in AWB is comprehensive and supported by strong data. This is a logically flowing and easy to read manuscript that will appeal to the readership of eLife.
While not the point of the experiment, it is interesting that ARL-13 localizes along the entire length of the AWB cilium. In amphid channel cilia, ARL-13 is restricted to the doublet/middle segment. Could authors comment on this?
In this paper, the authors report on the functions of a C. elegans Tubby homolog, TUB-1, in controlling the shape of sensory neuron cilia, and localization of sensory proteins within these compartments. The authors reveal that TUB-1 is required for both initial, and activity-dependent formation of ciliary elaborations, and that this is mediated in part by trafficking of a PIP5 kinase. Consistent with this, changes in phosphoinositides in ciliary membranes are documented.
Cilia are ubiquitous structures in animals, and are thought to adorn most mammalian cells. In general, these structures serve as signaling compartments, and understanding how these structures are formed and signaling proteins localized within them has broad implications for cell-cell signaling in the nervous system and outside the nervous system.
The studies presented here are outstanding in rigor and clarity. The authors' interpretations of their results are plausible and consistent with other observations in the field, but provide a step forward in implicating TUB-1 in neuronal plasticity. In my opinion, the paper is fine as is.
Nonetheless, if the authors are inclined, it would be interesting to understand more about the effects of tub-1 mutations on animal behavior. Are responses to environmental odors altered? Are these alterations consistent with the cell biological defects?https://doi.org/10.7554/eLife.48789.028
While not the point of the experiment, it is interesting that ARL-13 localizes along the entire length of the AWB cilium. In amphid channel cilia, ARL-13 is restricted to the doublet/middle segment. Could authors comment on this?
As the reviewer notes, the localization pattern of ARL-13 is indeed distinct between the AWB and channel cilia (first reported by Cevik et al., 2010). Since we do not currently know the reason or the mechanism underlying this cell-specific difference in subcellular localization pattern, we prefer to not speculate at this time.
Nonetheless, if the authors are inclined, it would be interesting to understand more about the effects of tub-1 mutations on animal behavior. Are responses to environmental odors altered? Are these alterations consistent with the cell biological defects?
A previous report showed that tub-1 mutants exhibit defects in their responses to a subset of volatile attractive odorants, including chemicals known to be sensed by AWC and AWA (Mak et al., 2006). We plan to follow up on these observations in the future with more detailed comparisons and analyses of the effects of tub-1 mutations on both odorant-evoked behaviors as well as neuronal activity in sensory neurons with ‘wing’ and ‘channel’ cilia.https://doi.org/10.7554/eLife.48789.029
- Piali Sengupta
- Alison Philbrook
- Danielle DiTirro
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We are grateful to the Caenorhabditis Genetics Center and Shohei Mitani (NRBP, Japan) for strains, Avital Rodal and Saikat Mukhopadhyay for reagents, and Avital Rodal, Steven Del Signore and Ashish Maurya for advice regarding FRAP. We thank the Sengupta lab and Saikat Mukhopadhyay for advice and comments on the work and manuscript. We are particularly grateful to Inna Nechipurenko for the illustration shown in Figure 8. This work was supported in part by the NIH (R35 GM122463 – PS.; T32 NS007292 – AP; T32 GM007122 – DD).
- Anna Akhmanova, Utrecht University, Netherlands
- Oliver Hobert, Howard Hughes Medical Institute, Columbia University, United States
- Maureen M Barr, Rutgers University, United States
© 2019, DiTirro 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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Heterodimeric motor organization of kinesin-II is essential for its function in anterograde IFT in ciliogenesis. However, the underlying mechanism is not well understood. In addition, the anterograde IFT velocity varies significantly in different organisms, but how this velocity affects ciliary length is not clear. We show that in Chlamydomonas motors are only stable as heterodimers in vivo, which is likely the key factor for the requirement of a heterodimer for IFT. Second, chimeric CrKinesin-II with human kinesin-II motor domains functioned in vitro and in vivo, leading to a ~2.8-fold reduced anterograde IFT velocity and a similar fold reduction in IFT injection rate that supposedly correlates with ciliary assembly activity. However, the ciliary length was only mildly reduced (~15%). Modelling analysis suggests a nonlinear scaling relationship between IFT velocity and ciliary length that can be accounted for by limitation of the motors and/or its ciliary cargoes, e.g. tubulin.
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