Previously we isolated a collection of maternal mutants defective in blastoderm cellularization and/or germ-band extension (Pimenta-Marques et al., 2008). Complementation group 7 contained two different mutant alleles with similar defects in blastoderm cellularization. Through deficiency mapping and a candidate gene approach we concluded that both were allelic to the uncharacterized coding gene CG6197 (Flybase). To confirm the mutants’ identity, we rescued their zygotic lethality, female sterility (germ-line clones), and blastoderm cellularization defects (maternal mutant embryos) using a genomic fragment construct that contained a wild-type copy of CG6197 (Figure 1—figure supplement 1A, data not shown). Both isolated alleles of CG6197 showed identical phenotypes: maternal mutant embryos (hereafter referred to as mutant embryos) showed normal syncytial nuclear divisions (Figure 1A,B) but subsequently failed to elongate the cortical nuclei, which became mislocalized during blastoderm cellularization (Figure 1C–F, quantification in Figure 1G). The blastoderm cellularization phenotype was remarkably similar to that described for kugelkern/charleston mutant embryos (Brandt et al., 2006; Pilot et al., 2006). Based on the observed phenotypes, we named the corresponding gene fandango, after the Iberian folk dance.

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fandango encodes the Drosophila ortholog of yeast SYF1 (synthetic lethal with cdc41) (Russell et al., 2000) and human XAB2 (XPA binding protein 2) (Nakatsu et al., 2000; Kuraoka et al., 2008). These proteins were described as subunits of the NTC/Prp19 complexes, which are important for spliceosome stabilization and activation (Chan et al., 2003; Chang et al., 2009; Hogg et al., 2010). Fandango protein has multiple tetratricopeptide repeat (TPR) motifs, which is a protein–protein interaction module (Zeytuni and Zarivach, 2012). Sequencing both alleles of fandango (fand¹ and fand²) revealed distinct mutations within the fandango open reading frame (ORF). fand¹ contained a missense point mutation in a highly conserved residue within TPR domain VII (from an alanine to a valine; A401V), whereas fand² contained a microdeletion of 18 nucleotides within TPR domain VI, which deleted six conserved amino acids from position 355 to 360 (Figure 1—figure supplement 1B). In total protein extracts, both fand¹ and fand² mutant embryos showed a significant reduction in Fandango protein levels compared to control (Figure 1I). fandango mRNA levels, analyzed by real-time qPCR, were similar between control and fand¹ mutant embryos (Figure 1J), suggesting that the mutation did not alter the stability of the encoding pre-mRNA.

As noted above fandango maternal mutant embryos and kugelkern (kuk) mutant embryos showed remarkably similar blastoderm cellularization defects (Brandt et al., 2006; Pilot et al., 2006). Since fandango encodes a protein whose yeast and human orthologs are required for efficient spliceosome activity, we hypothesized that Fandango was required for splicing of kuk transcripts. kuk encodes two different transcripts, which vary in intron size (Figure 2A). Both transcripts are predicted to encode the same protein. Analysis of publicly available modENCODE transcriptome datasets (Graveley et al., 2011) suggested that the large kuk transcript was maternally expressed, whereas the small kuk transcript was only expressed zygotically. Through RT-PCR analysis we confirmed that similarly to control maternal genes (nanos and oskar) the large kuk transcript was maternally expressed (being present in unfertilized eggs), whereas the small kuk transcript was exclusively zygotically expressed (being present only in fertilized eggs) as the case of well-known early zygotic genes (even-skipped and krüppel) (Figure 2—figure supplement 1A).

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To investigate by RT-PCR whether Fandango was required for splicing of kuk pre-mRNAs, specific sets of primers (exon–exon, e–e; intron–exon, i–e) were designed for each kuk transcript, taking advantage of a longer 3′UTR in the small kuk transcript (Figure 2A). Surprisingly, whereas fandango embryos showed significant splicing defects of the small zygotic kuk transcript, the large maternal kuk transcript was correctly spliced (Figure 2B; Figure 2—figure supplement 1B). Splicing defects were fully rescued by a genomic fragment construct that contained a wild type copy of fandango (Figure 2—figure supplement 1C). The differential requirement of Fandango for splicing of kuk transcripts prompted us to investigate more than 20 other maternal and early zygotic genes. RT-PCR analysis of fandango embryos invariably showed splicing defects of early zygotic but not maternally encoded transcripts (Figure 2C, data not shown). High-throughput transcriptome sequencing (RNAseq) confirmed that splicing of early zygotic but not maternally encoded gene products was affected in fandango embryos (Figure 2D, Figure 2—figure supplement 2A). Maternal transcripts, whose intron size was equivalent to those observed in early zygotic transcripts, were unaffected (Figure 2—figure supplement 2B), which showed that Fandango was not specifically rate limiting for splicing of small introns. Comparison analysis of 5′ and 3′ splice site consensus sequences between maternal and zygotic pre-mRNA transcripts showed no significant differences (Figure 2—figure supplement 2C) and the two populations of transcripts displayed a similarly heterogeneous exon–intron structure (Figure 2—figure supplement 2D). RT-PCR analysis of maternally encoded transcripts from wild-type and fandango mutant ovaries (germ-line clones) also failed to detect splicing defects (Figure 2—figure supplement 1D). This suggested that the absence of splicing defects of maternally encoded transcripts in fandango embryos was not due to specific degradation of unspliced transcripts during oogenesis.

The differential requirement of Fandango for splicing of early zygotic encoded transcripts is fully consistent with the observation that maternally controlled oogenesis, primordial germ-cell formation, and syncytial nuclear divisions were normal in fandango mutants (Figure 1A,B,H,K,L), whereas the first detectable phenotype only occurred during zygotically controlled blastoderm cellularization (Figure 1C–F). Despite the fact that clonal analysis of the female germ line for both alleles of fandango showed normal oogenesis and egg laying (Figure 1H) (data not shown), Fandango protein levels were significantly reduced in the mutant ovaries (germ-line clones) (Figure 1I). fandango embryos also failed to initiate germ-band extension after blastoderm cellularization (data not shown). It was previously shown that anterior–posterior (A–P) patterning is required for germ-band extension (Zallen and Wieschaus, 2004). Consistently, fandango embryos showed A–P patterning defects in the early zygotic pair-rule gene even-skipped (Figure 1M,N).

The highly conserved NTC/Prp19 and NTC/Prp19-related complexes are essential for pre-mRNA splicing as they facilitate the formation and progression between distinct spliceosome conformations during the splicing reaction (Chan et al., 2003; Hogg et al., 2010).

Endogenous Fandango and Prp19 physically interacted in the early embryo (Figure 3A). Moreover, both endogenous Fandango and Prp19 physically interacted with endogenous ISY1 and CDC5L (Figure 3A), confirming that Fandango is a bona fide subunit of Drosophila NTC/Prp19 complexes. Immunoprecipitation of Myc-tagged Fandango and Myc-tagged Prp19 from embryonic protein extracts also identified an identical group of interacting proteins (Table 1; Supplementary file 1). Whereas Myc-Fandango mostly interacted with the NTC/Prp19-related complex subunits, Myc-Prp19 interacted principally with the NTC/Prp19 complex subunits. This illustrated that, as in humans, distinct but interacting NTC/Prp19 complexes exist in Drosophila, in agreement with the recent suggestion that a remarkable degree of conservation of distinct splicing complexes exists among metazoans (Herold et al., 2009).

Figure 3

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The differential requirements of Fandango for pre-mRNA splicing of maternal and early zygotic transcripts potentially suggest distinct interactions between Fandango and other splicing proteins during oogenesis and early embryonic development. Nevertheless, immunoprecipitation of Myc-Fandango specifically expressed in the female germ line during oogenesis and in the early embryo identified a virtually identical group of interacting proteins: mostly subunits of the NTC/Prp19-related complex, and to a lesser extent, subunits of the NTC/Prp19 complex (Table 1; Supplementary file 1). These results showed that Fandango physically interacts with a similar group of splicing proteins during oogenesis and in the early embryo.

To better understand the splicing defects observed in fandango embryos, we investigated if the integrity of NTC/Prp19 complexes was affected in this mutant. Size-exclusion chromatography showed detectable changes in the integrity of NTC/Prp19 complexes in fandango embryos (Figure 3B), with a significant reduction in the levels of ISY1 protein (Figure 3C). ISY1 is a NTC/Prp19-related complex subunit (Figure 3A). The loss of integrity of the ISY1-positive ∼600–800 kDa NTC/Prp19 complex (Figure 3B) and concomitant reduction in the stability of some of their subunits, most likely impaired efficient activation of the spliceosome (Villa and Guthrie, 2005) and were likely explanations for the splicing defects observed in fandango embryos. In agreement with the suboptimal spliceosome activation hypothesis, intron retention was the main splicing defect of early zygotic transcripts in fandango embryos (Figure 2B,C, Figure 2—figure supplement 2B; data not shown).

Levels of ISY1 were similarly affected in fandango mutants during oogenesis and in the early embryo (Figure 3C), suggesting this decrease did not explain the differential requirements of Fandango for splicing of early zygotic and maternally encoded transcripts. Mutant clonal analysis of a stronger allele of fandango (nonsense mutation), showed a complete loss of the female germ line in adult ovaries (data not shown). This demonstrated that the two isolated alleles of fandango are hypomorphic and suggested that Fandango was required, albeit at lower levels, for splicing of maternal transcripts. We concluded it is unlikely that a differential expression and/or association of core components of the spliceosome could potentially explain the differential requirements for Fandango between oogenesis and the early embryo. The most likely explanation is that Fandango is quantitatively (but not qualitatively) differentially required during early embryonic development.

Transcriptional elongation can affect co-transcriptional splicing (de la Mata et al., 2003; Ip et al., 2011). It was recently shown that Syf1, the yeast ortholog of Fandango, is also important for RNApol II transcriptional activity (Chanarat et al., 2011; David et al., 2011), therefore we decided to investigate transcription in fandango embryos. Three intronless early zygotic genes (nullo, snail, and scute) and two early zygotic genes with introns (even-skipped and tailless) were selected for further analysis by real-time qPCR. During mid/late-syncytial blastoderm (stage B) (Figure 4A, ‘Materials and methods’), no significant differences in transcript abundance were observed between control and fandango (Figure 4—figure supplement 1A), whereas embryos mutant for grapes showed the expected reduction of transcript levels (Figure 4—figure supplement 1A; Sibon et al., 1997).

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During transcriptional elongation, RNApol II is specifically phosphorylated on the Ser2 residue of its carboxy-terminal domain (CTD) (Hsin and Manley, 2012). In agreement with the onset of early zygotic transcription, we observed a significant increase in RNApol II CTD Ser2 phosphorylation as the embryo developed from early/mid-syncytial blastoderm (stage A), into mid/late-syncytial blastoderm (stage B), and blastoderm cellularization (interphase 14) (stage C) (Figure 4A,B). Both control and fandango embryos showed a similar increase in global levels of RNApol II CTD Ser2 phosphorylation (Figure 4B,C). As transcriptional regulation during interphase 14 (stage C) relies on correct expression of early zygotic genes and degradation of many maternal RNAs (MZT) (Tadros and Lipshitz, 2009), we concluded that transcriptional changes at this stage (Figure 4—figure supplement 1A) were most likely a consequence of the widespread defects occurring during mid/late-syncytial blastoderm. Altogether, we concluded that the observed reduction in Fandango levels affects mainly its splicing function.

To investigate if the differential requirement of Fandango for splicing of early zygotic and maternally encoded transcripts potentially resulted from distinct transcript sequences, we generated an early zygotic kuk transcript (kuk-LacZ) under the control of an UAS/Gal4 inducible promoter, where the open reading frame (ORF) was replaced by LacZ (Figure 5A, see ‘Materials and methods’ for more details). As expected, when this construct was expressed zygotically, it was correctly spliced in control but not in fandango embryos (Figure 5B). In contrast, splicing of the kuk-LacZ construct occurred normally in both control and fandango mutants when it was expressed maternally (Figure 5B). Since maternal expression of an early zygotic transcript, in a fandango mutant background, was enough to suppress its splicing defects, we concluded that the differential requirement of Fandango for splicing of early zygotic transcripts was most likely due to the developmental context of gene expression and not a particularity in the early zygotic pre-mRNA sequences. Consistently, we failed to detect differences related to intron size, splice sites consensus, and exon–intron structure between maternal and zygotic transcripts (Figure 2—figure supplement 2B–D).

Figure 5

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fandango mutants showed a significant reduction in Fandango and ISY1 protein levels (Figure 3C), which most likely impaired efficient activation of the spliceosome (Villa and Guthrie, 2005). Since mitosis inhibits splicing (Shin and Manley, 2002), pre-mRNA splicing of early zygotic transcripts needs to be highly efficient for these genes to be correctly expressed. This suggests the existence of a developmental pre-requisite for highly efficient splicing, so that a suboptimal activation of the spliceosome would specifically impair pre-mRNA splicing of early zygotic but not maternal transcripts. Wild-type embryos already showed a detectable amount of intron retention in early zygotic transcripts (Figure 2B,D, Figure 2—figure supplement 2B), which was dramatically exacerbated in fandango embryos (Figure 2B,D, Figure 2—figure supplement 2B).

We hypothesized that regardless of transcript size, there was also a constraint on pre-mRNA splicing of early zygotic transcripts in wild-type embryos. We generated a gene where the 5′UTR sequence including the intron of the small zygotic kuk transcript was quadruplicate to test this hypothesis (Figure 6A,D see ‘Materials and methods’ for more details). Quadruplicate introns were linked by in-frame LacZ coding sequences, and the entire construct (4x intron kuk-LacZ) was under the control either of an endogenous early zygotic minimal promoter (nullo-4x intron kuk-LacZ, ∼2.5 Kb) (Figure 6A) or an inducible UAS/Gal4 promoter (UAS-4x intron kuk-LacZ, ∼2.5 Kb) (Figure 6D). The total size of the encoded pre-mRNAs was comparable to many other endogenous early zygotic genes (e.g., kugelkern, runt, krupple). As a control, we introduced point mutations in the splice sites of these constructs to generate comparable intronless transcripts (no intron kuk-LacZ) (Figure 6A,D).

Figure 6

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Only the first intron (int1) of the 4x intron kuk-LacZ construct was correctly spliced when it was zygotically expressed in wild-type embryos under the control of an endogenous early zygotic minimal promoter (Figure 6B). Likewise, when the 4x intron kuk-LacZ construct was early zygotically expressed under the control of the inducible promoter UAS/Gal4 there were similar splicing defects (intron retention) (Figure 6E).

Measurement of in vivo kinetics of mRNA splicing showed that half-lives for splicing reactions are <1 min for the first intron, but 2–8 min for both second and third introns (Audibert et al., 2002). Hence, splicing of two or more introns requires more time than transcription and becomes rate limiting. Consistent with the hypothesis of a temporal constraint on pre-mRNA splicing, when the 4x intron kuk-LacZ construct was zygotically expressed, the splicing defects of the firstly transcribed 5′-localized introns (Int1 and Int2) were significantly weaker than those observed in the later transcribed 3′-localized introns (Int3 and Int4) (Figure 6E). Importantly, maternal expression of this construct was sufficient to significantly suppress its splicing defects (Figure 6E). Real-time qPCR analysis showed that these constructs were equivalently zygotically and maternally expressed (Figure 6C,F). This suggested that splicing did not quantitatively impair early zygotic transcription, which was consistent with the observation that the rates of transcriptional elongation proceed independently of splicing (Brody et al., 2011).

We showed that in wild-type embryos pre-mRNA splicing imposed significant constraints on early zygotic expression, which is a likely explanation why most early zygotic genes are intronless (De Renzis et al., 2007). Although a moderate decrease in the length of syncytial blastoderm interphases (seen in grapes mutant embryos [Sibon et al., 1997]) was not sufficient to induce splicing defects in otherwise wild-type embryos (data not shown), we hypothesize that avoidance of pre-mRNA splicing during early zygotic expression is a consequence of the extremely short interphases and frequent mitotic cycles. Similarly to Drosophila, mosquito Aedes aegypti and the zebrafish Danio rerio early zygotic transcripts are frequently intronless when compared with the rest of the transcriptome (Biedler et al., 2012; Heyn et al., 2014). This suggests that highly proliferative tissues need coordination between cell cycle and gene architecture for correct gene expression and avoidance of abnormally processed transcripts.

Our results highlight cell cycle constraints during early embryonic development as a force capable of driving changes in gene architecture of multicellular organisms. In unicellular organisms intron paucity correlates with a bias toward the 5′ ends, whereas introns from multicellular genomes are evenly distributed throughout the genes (Mourier and Jeffares, 2003). This suggests that similar constraints on gene architecture are also likely to exist in yeast and other fast-dividing single cell eukaryotes.

The way splicing efficiency might be regulated through changes in constitutive spliceosome factors and how it might influence differential gene expression is a new area of interest. In this study, we present experimental evidence supporting the hypothesis of a requirement for highly efficient pre-mRNA splicing during early embryonic development. Since the NTC/Prp19 complexes are known to be important for efficient spliceosome activation, and our mutant alleles specifically impaired pre-mRNA splicing of early zygotic but not maternally encoded transcripts, we propose that overall requirements for splicing efficiency are likely to vary during development, being the NTC/Prp19 complexes a key modulator of spliceosome activation rates. In agreement with this hypothesis, Prp19 expression varies during neuronal differentiation (Urano et al., 2006).

In plants it was recently shown that removal of retained introns regulates translation in rapidly developing gametophytes (Boothby et al., 2013). In Drosophila, a sub-population of early zygotic transcripts with introns similarly showed some degree of intron retention in wild-type embryos (Figure 2B,D, Figure 2—figure supplement 2B). Our results also suggest that the pre-requisite for highly efficient splicing during early embryonic development is paradoxically also likely to play an important regulatory role in the expression of a subset of early zygotic transcripts, which further supports the possibility that modulation of spliceosome activation per se is important for differential regulation of gene expression during development.

Flies were raised using standard techniques. The fandango alleles were isolated in a previously reported maternal screen (Pimenta-Marques et al., 2008). Maternal mutant embryos and germ-line mutant clones were generated using the FLP/FRT ovo^D system (Chou and Perrimon, 1992). Germ-line clones of fand¹ and fand² were established by crossing FRT42B fand¹/CyO or FRT42B fand²/CyO virgins to hs-FLP; FRT42B ovo^D/CyO males and the progeny was heat shocked once at 37°C for 1 hr during second and third larval instar stages. As control we generated germ-line clones with FRT42B by crossing FRT42B/CyO virgins to hs-FLP; FRT42B ovo^D/CyO males and followed by the heat shock procedure described before.

To generate homozygous mutant clones in ovaries for fand¹ (negative for nuclear GFP label, nGFPminus) we used FLP/FRT to induce mitotic recombination. Females y, w, hs-FLP; FRT42B nGFP/CyO hs-hid flies were crossed with w; FRT42B, fand¹/CyO hs-hid males. Recombination was induced by 1-hr heat shock at 37°C at second and third instar larval stage. Adult ovaries were harvested from 4–5-day-old females and subsequently processed for immunofluorescence.

Viability and phenotypes of fandango alleles were complemented by crossing a transgenic fly carrying a genomic fragment construct that contained a wild-type copy of CG6197 (wt-fandango). w; FRT42B, fand¹/CyO virgins were crossed to wt-fandango; FRT42B, fand²/CyO males; reciprocal crosses were also performed. Offspring were counted to determine viability. Rescue of maternal phenotypes (cellularized blastoderm defects and splicing defects in early zygotic transcripts) was also analyzed in embryos laid by F1 wt-fandango/ +; FRT42B, fand¹/FRT42B fand² females. Germ-line clones of fand¹ and fand² were also rescued (cellularized blastoderm defects and splicing defects in early zygotic transcripts) by a copy of wt-fandango in the third chromosome. FRT42B fand¹/CyO; wt-fandango or FRT42B fand²/CyO; wt-fandango virgins were crossed with hs-FLP; FRT42B ovo^D/CyO males and heat shock performed as described above.

To induce maternal and zygotic expression of the UAS-kuk-LacZ construct in control and fandango maternal mutant embryos, we performed the following crosses:

Maternal expression in control genetic background: virgin females +/+; Nanos-Gal4, UAS-kuk-LacZ/TM6B crossed with wild-type males.

Zygotic expression in control genetic background: virgin females +/+; actin-Gal4/TM6B crossed with +/+; UAS-kuk-LacZ males.

Maternal expression in fandango maternal mutant genetic background: firstly, virgin females FRT42B fand¹/CyO; Nanos-Gal4, UAS-kuk-LacZ/TM6B crossed with hs-FLP; FRT42B ovo^D/CyO males, and heat shocked as described above. After eclosion, Cy⁺ and Tb⁺ females were selected from the progeny and crossed to wild-type males.

Zygotic expression in fandango maternal mutant genetic background: firstly, virgin females FRT42B fand¹/CyO; actin-Gal4/TM6B were crossed with hs-FLP; FRT42B ovo^D/CyO males, and heat shocked as described. After eclosion, Cy⁺ and Tb⁺ virgin females were selected from the progeny and crossed to +/+; UAS-kuk-LacZ males.

To induce maternal and zygotic expression of the 4x intron kuk-LacZ and no intron kuk-LacZ constructs we performed following crosses:

Maternal expression: firstly, virgin females +/+; actin-Gal4/TM6B crossed with +/+; UAS-4xintron-kuk-LacZ/TM6B or UAS-nointron-kuk-LacZ/TM6B males. After eclosion, females Tb⁺ (+/+; actin-Gal4/UAS-4xintron-kuk-LacZ or +/+; actin-Gal4/UAS-nointron-kuk-LacZ) were selected and crossed with wild-type males.

Zygotic expression: virgin females +/+; actin-Gal4/TM6B were crossed with +/+; UAS-4xintron-kuk-LacZ/TM6B or UAS-nointron-kuk-LacZ/TM6B males.

To analyze zygotic expression of the 4x intron kuk-LacZ and no intron kuk-LacZ constructs under the control of the minimal promoter of the gene nullo, females carrying the corresponding construct were selected and crossed with wild-type males.

To drive embryonic and ovarian expression of Myc-tagged Fandango and Myc-tagged Prp19 proteins, Nanos-Gal4 homozygous virgins were crossed with UAS-Fandango-6xMyc males or UAS-Prp19-6xMyc/TM6B males, respectively. After eclosion females (in case of Myc-Fandango) or Tb⁺ females (in case of Myc-Prp19) were selected, dissected ovaries from 4–5-day-old females, or laid embryos after a cross with wild-type males were used for protein extraction.

To identify the gene responsible for lethality in fandango alleles, we performed a complementation analysis using the Bloomington 2R Deficiency kit.

Deficiency Df(2R)CX1 (covering an interval from cytological band 49C1 to 50D2, Bloomington stock number 442) failed to complement zygotic viability of both fandango alleles (complementation group 7). All additional 22 overlapping deficiencies complemented both fandango alleles. The cytological interval between bands 50B4-B6 (comprising 6 genes) was not covered by the 22 deficiencies. We cloned and sequenced these 6 genes from genomic DNA of both control and fandango alleles and identified mutations in gene CG6197 in both fandango alleles.

To confirm the identity of our mutants, we digested DNA from genomic clone (BACR14P04, Flybase) with restriction enzymes XbaI and EcoRI to generate a genomic fragment comprising the wild-type gene sequence of CG6197 (wt-fandango). Then we cloned the fragment into pCasper vector and used it to generate transgenic stocks (Bestgene, Chino Hills, CA, USA). A genomic wild-type copy of CG6197 under the control of its endogenous promoter fully complemented all known phenotypes in both fandango alleles.

0–3 hr (after egg laying) embryos, both maternally mutant for fandango and control, were fixed and stained using standard procedures (Pimenta-Marques et al., 2008). For Neurotactin and Slam immunostaining, the fixation procedure was modified: embryos were added to boiling heat fix solution (68 mM NaCl +0.1% Triton) and stirred for 1 min, then cooled by adding an equal volume of cooled fix solution. Immunostaining for oogenesis phenotypic analysis was performed as described in Guilgur et al. (2012). Following primary antibodies used were: mouse anti-Neurotactin clone BP106 at 1:133 (DSHB, Iowa City, Iowa, USA); mouse anti-pTyr at 1:1000 (9411; Cell Signaling, Danvers, MA, USA), and rabbit anti-slam at 1:1000 (Ruth Lehman Lab). For F-actin staining, a 5-min incubation with phalloidin-Rhodamine at 1:200 dilution (Sigma, St Louis, MO, USA; stock concentration 1 mg/ml) was employed at room temperature. For DNA staining, we used SYTOX Green (Invitrogen, Grand Island, NY, USA) at 1:5000 dilution with 5 mg/ml RNase A in PBT (PBS+0.1% Tween-20) for 30 min at room temperature. Cy3- or Cy5-conjugated secondary antibodies were used at 1:1000 dilution (Jackson ImmunoResearch, West Grove, PA, USA) and anti-rabbit Alexa Fluor 488 at 1:1000 dilution (Molecular Probes, Grand Island, NY, USA).

The kuk-LacZ construct was synthesized using the 5′UTR and intron of the kuk small transcript (kuk-RB, Flybase). The kuk ORF was replaced by the LacZ coding sequence and was followed by the 3′ UTR of the original transcript (Figure 5A). The kuk-LacZ construct was fused to a UASg promoter (Gateway system, Invitrogen, Grand Island, NY, USA).

The 4x intron kuk-LacZ construct was synthesized using 4 repeats of the fragment of 5′UTR and intron of the kuk small transcript, separated by 201 nucleotides of in-frame LacZ sequence. The stop codon is followed by the 3′UTR kuk small transcript sequence and 300 bp of the 3′-located genomic region to promote transcriptional termination (Figure 6A,D). In the case of the no intron kuk-LacZ, all splice sites (meaning 5′ splice site, branch point, and 3′ splice site) were mutated to thymidines (Figure 6A,D). To induce expression of these constructs, they were fused to UAS promoter or nullo minimal promoter. The 4x intron kuk-LacZ and no intron kuk-LacZ constructs were cloned into pWALIUM22.

Fandango open reading frame, kuk-LacZ, 4x intron kuk-LacZ, and no intron kuk-LacZ constructs were synthetized (GenScript, Piscataway, NJ, USA). Prp19 open reading frame was cloned into pDONR221 from DGC gold BDGP clone LD09231.

Prp19 and Fandango ORFs were subcloned into a vector containing the UASp promoter and 6x C-terminal Myc-tag (Gateway, Invitrogen, Grand Island, NY, USA). All constructs were then used to generate transgenic flies stocks (BestGene, Chino Hills, CA, USA).

Total RNA was extracted from 0–3 hr (after egg laying) embryos, unfertilized embryos, and 4-day-old female ovaries mutant for fandango and control (FRT42B) following standard procedures (PureLink RNA Mini Kit, Ambion, Grand Island, NY, USA). 1 μg of RNA was then used for reverse transcription with Oligo(dT)12–18 and/or random hexamers primers following the manufacturer’s protocol (Transcriptor First Strand cDNA Synthesis Kit, ROCHE, Germany). Primer combinations used were designed with PrimerSelect (Lasergene, Madison, WI, USA) and PCR was performed using GoTaq DNA polymerase (Promega, Fitchburg, WI, USA). Sequences of all primers used are listed in Supplementary file 2.

To measure transcription levels, embryos were staged in three different groups based on the embryonic morphology: stage A (embryos from cycle 1 to 8, no pole cells, and no cortical nuclei are observed); stage B (embryos from cycle 8/9 to 13, pole cells present, and cortical nuclei are observed); and stage C (embryos at interphase 14, blastoderm cellularized). Three independent replicas for each stage, containing each 10 manually selected embryos were generated. Three different genetic backgrounds were analyzed (control (FRT42B), FRT42B fandango, and grapes as positive control). To measure fandango mRNA levels, unfertilized eggs were analyzed (three replicas). To measure transcription level of the 4x intron kuk-LacZ and no intron kuk-LacZ constructs, 0–3 hr (after egg laying) embryo collections were used to analyze both maternal and zygotic induced expression.

Total RNA was extracted from samples and then used for reverse transcription with Oligo(dT)12–18 as described above. Real-time mRNA quantification was performed following the manufacturer’s protocol (QuantiFast SYBR Green RT-PCR Kit, Qiagen, Germany). For analysis of transcription levels of early zygotic genes (nullo, snail, scute, even-skipped, and tailless) the Drosophila QuantiTect Primer Assay (Qiagen, Germany) was used. For mRNA level measurements of fandango, 4x intron kuk-LacZ and no intron kuk-LacZ constructs primers were designed with Primer3 (Supplementary file 2).

Anti-Fandango and anti-Prp19 rabbit polyclonal antibodies were raised against recombinant proteins corresponding to amino acids 551–750 of Fandango/CG6197-PA, and to amino acids 20–219 of Prp19-PA, respectively (Metabion international AG, Germany). In both cases it was used His-tagged recombinant proteins as antigen and the antibodies were affinity purified.

Protein extracts were obtained from 0–3 hr (after egg laying) embryos or 4-day-old female ovaries. Embryos were dechorionated with 50% commercial bleach solution and ovaries dissected in PBS, samples then homogenized in NB buffer (150 mM NaCl, 50 mM Tris–HCl pH 7,5, 2 mM EDTA, 0,1% NP-40, 1 mM DTT, 10 mM NaF, and EDTA-free protease inhibitor cocktail, Roche, Germany), and centrifuge at 20000×g for 3 min. Supernatant was recovered and centrifuged twice.

To analyze NTC/Prp19 complex composition (Table 1), co-immunoprecipitation was done using protein extracts from embryo or ovary tissues expressing Myc-tagged Fandango or Prp19. Briefly, 1 mg of protein was diluted in 1 ml NB buffer and incubated with 1 µg/ml of mouse c-Myc antiboby (9E10) (Santa Cruz Biotechnology, Dallas, Texas, USA) for 1 hr at 4°C. Subsequently, 0.9 mg of Dynabeads Protein G (Invitrogen, Grand Island, NY, USA) were added to the immune complex and incubated 1 hr at 4°C. Beads were washed three times with NB buffer and protein elution performed with 50 µl of 100 mM Glycine pH 2.5 during 2 min at RT and stopped with 5 µl of 1M Tris–HCl pH 10.85. Eluted proteins were then precipitated in five times the volume of acetone at −20°C and samples analyzed by liquid chromatography coupled to tandem mass spectrometry (Mass Spectrometry Laboratory, Institute of Biochemistry and Biophysics, Poland).

To analyze NTC/Prp19 complex composition (showed in Figure 3A), protein co-immunoprecipitation was performed using nuclear protein extracts (adapted from Kamakaka and Kadonaga, 1994) from a collection of 0–3 hr (after egg laying) wild-type embryos (Oregon-R). 1 mg of protein extract was incubated with rabbit anti-Prp19 (1:1000 dilution) or the pre-immune (1:10,000 dilution) as control, in HNEB2 buffer (100 mM NaCl, 2,5 mM MgCl₂, 10 mM Tris–HCl pH 7,5, 0,5% Triton X-100, and EDTA-free protease inhibitor cocktail, Roche, Germany) during 1 hr at 4°C. The procedure was carried out as described in previous co-immunoprecipitation and eluted complexes were boiled in Laemmli sample buffer and analyzed by Western Blot.

Size-exclusion chromatography was performed in protein extracts of 0–3 hr (after egg laying) embryo collections from FRT42B fand¹ mutants or control (FRT42B). Extracts were prepared as described before in NB2 buffer (150 mM NaCl, 50 mM Tris–HCl pH 7,5, 2 mM EDTA, 0,01% NP-40, 1 mM DTT, and EDTA-free protease inhibitor cocktail, Roche, Germany). Subsequently, 2 mg of protein extract were fractionated using Superose 6 10/300 GL column (GE Healthcare, United Kingdom) in NB2 buffer and fractions collected and analyzed by Western blot.

To analyze protein amount in ovaries and embryos (showed in Figures 1I and 3C), embryos were dechorionated and ovaries dissected as described above. Samples were homogenized in PBS supplemented with EDTA-free protease inhibitor cocktail (Roche, Germany) and centrifuged at 20000×g for 3 min at 4°C. Supernatant was collected and protein concentration determined using the Bradford method (BioRad, Hercules, CA, USA). Samples were immediately boiled in Laemmli sample buffer and 10 µg of protein was run in SDS-PAGE gel and analyzed by immunoblot.

Levels of RNApol II CTD Ser2 phosphorylation were analyzed in embryos dechorionated and manually selected at specific developmental stages based on the embryonic morphology (as described above). 15 embryos were selected for each stage and protein sample was obtained by lysing the embryos with a needle in Laemmli sample buffer and heating for 5 min at 100°C. Protein amounts corresponding to ∼7 embryos were running in SDS-PAGE and analyzed by immunoblot. Five independent replicas were analyzed.

Antibodies used were: polyclonal rabbit anti-Prp19 at 1:8000 dilution; polyclonal rabbit anti-Fandango at 1:1000 dilution; mouse anti-alpha-Tubulin Dm1A at 1:50,000 dilution (Sigma, St Louis, MO, USA); mouse anti-RNA Polymerase II H5 at 1:500 dilution (MMS-129R, Covance, Princeton, NJ, USA); rabbit anti-ISY1 at 1:500 dilution (ab121250; Abcam, United Kingdom); and mouse anti-CDC5L [2136C1a] at 1:200 dilution (ab51320; Abcam, United Kingdom).

Peptides mixtures were analyzed by LC-MS-MS/MS (liquid chromatography coupled to tandem mass spectrometry) using Nano-Acquity (Waters, Milford, MA, USA) LC system and Orbitrap Velos mass spectrometer (Thermo Electron Corp., San Jose, CA, USA). Prior to analysis, proteins were subjected to standard ‘in-solution digestion’ procedure, during which proteins were reduced with 100 mM DTT (for 30 min at 56°C), alkylated with 0,5 M iodoacetamide (45 min in darkroom at room temperature), and digested overnight with trypsin (sequencing Grade Modified Trypsin—Promega V5111). The peptide mixture was applied to an RP-18 precolumn (nanoACQUITY Symmetry C18—Waters 186003514) using water containing 0,1% TFA as mobile phase, then transferred to nano-HPLC RP-18 column (nanoACQUITY BEH C18–Waters 186003545) using an acetonitrile gradient (0%–35% AcN in 180 min) in the presence of 0.05% formic acid with a flow rate of 250 nl/min. The column outlet was directly coupled to the ion source of the spectrometer, operating in the regime of data dependent MS to MS/MS switch. A blank run ensuring no cross contamination from previous samples preceded each analysis.

Raw data were processed by Mascot Distiller followed by Mascot Search (Matrix Science, London, UK, on-site license) against Flybase database. Search parameters for precursor and product ions mass tolerance were 100 ppm and 0.6 Da, respectively, enzyme specificity: trypsin, missed cleavage sites allowed: 0, fixed modification of cysteine by carbamidomethylation, and variable modification of methionine oxidation. Peptides with Mascot Score exceeding the threshold value corresponding to <5% False Positive Rate, calculated by Mascot procedure, and with the Mascot score above 30 were considered to be positively identified.

Human orthologs were determined using DSRC Integrative Ortholog Prediction Tool (DIOPT) (http://www.flyrnai.org/cgi-bin/DRSC_orthologs.pl). Only scores above two were considered such as the best matches when there was more than one match per input.

Total RNA was isolated from 0–3 hr collections of fandango maternal mutant and control (FRT42B) embryos using TRIzol Reagent (Invitrogen, Grand Island, NY, USA), following standard protocol. DNAse I (Promega, Fitchburg, WI, USA) treatment was performed during 30 min at 37°C. DNAse was extracted by Phenol-Chloroform extraction; the RNA was precipitated with ethanol, and dissolved it in 25 µl of DEPC water. Bioanalyzer testing was used to analyze quality and concentration of the samples and made up to the volume to 100 µl with water, 50 µl of 7.5 M NH4OAc added, 0.5 µl of glycogen, and 250 µl of absolute ethanol. cDNA library was generated applying the standard Illumina protocol for RNA-Seq (polyA RNAs) and sequenced with an Illumina HiSeq (Oklahoma Medical Research Foundation, Oklahoma City, OK, USA). These generated RNA-Seq data for two biological replicates each of wild-type and fandango mutant (fand¹), consisting of about 150 million illumina paired-end 100 bp reads per sample.

Paired-end reads were mapped with tophat (Trapnell et al., 2009) version 2.0.3 against the Drosophila melanogaster BDGP5 reference genome, using Flybase gene annotations downloaded from Ensembl e66 as guide.

To analyze splicing defects, we first extracted exon–intron boundaries from gene annotations. To avoid potential confounding effects, we removed all boundaries that had overlapping exon sequence (from different genes or transcripts). Subsequent analysis used this set of ‘safe’ exon–intron boundaries.

For coverage plots in Figure 2D, we also excluded boundaries where the intron or the exon were less than 50 b long. At each base within 50 bp either side of a splice site we count the number of reads that overlap that base, then divide by the total number of reads within the 100 bp centered around the splice site. To minimize noise, we require that at least 50 reads fall within the −50:50 window around the exon–intron boundary (reads that only partially overlap the window are also counted).

To determine the frequency of splicing defects for each boundary, we extracted all reads that overlap the 5′ splice site by at least 10 bp to either side of the boundary. We classified each read as correctly spliced (if the read is split from the 5′ to the 3′ splice site), unspliced (if the read is not split) or mis-spliced (if the read is split but not matching the expected 5′ or/and 3′ sites). To reduce noise, we only include an exon–intron boundary if at least 10 fragments overlap that boundary.

To determine the exon–intron gene structure (Figure 2—figure supplement 2D), each gene was divided in 1000 equal segments. For each segment of each gene, we checked for the presence (or absence) of an exon in that segment. For each segment, we then plotted the frequency of exon presence in all genes. If an exon randomly appears in a given segment, it appears in ∼50% of genes. For example, a set of intronless genes would produce a plot that would be always at 100%.

To determine the splice site motif (Figure 2—figure supplement 2C), sequences around exon–intron boundaries were extracted and motifs drawn using Weblogo.

Early zygotic and maternal genes were defined using RNA-Seq developmental gene expression data from Flybase (Graveley et al., 2011). A gene was defined as an early zygotic gene when its expression at 2–4 hr is at least moderate (more than 10 expression units, as defined in the Flybase dataset) and at least 5× greater than its expression at 0–2 hr (irrespective of the 0–2 hr value). Maternal genes are those genes that are not early zygotic and have high expression (more than 50 expression units) at 0–2 hr. To avoid potential artifacts, genes that have an extremely high expression (more than 1000 expression units) were not considered. Applying this definition we obtained 270 early zygotic genes (including 43 genes from De Renzis et al., 2007) and 2048 maternal genes.

All scripts used for this analysis are available upon request. RNA-Seq data are available in the ArrayExpress database (www.ebi.ac.uk/arrayexpress) under accession number E-MTAB-2321.

The procedure has been described in Stein et al. (2002). Antisense digoxigenin-labeled RNA probes were synthesized using the DIG RNA labeling Kit (Roche, Germany). eve and nos probes were made from pBluescript plasmids containing the respective cDNAs.

Sequences were aligned using ClustalW2 (http://www.ebi.ac.uk/Tools/msa/clustalw2/) and BoxShade 3.21 (http://www.ch.embnet.org/software/BOX_form.html) for printing and shading of multiple alignment file.

Unpaired t test and two-way ANOVA were performed using Prism 5.00 for Windows (GraphPad Software, San Diego, CA, USA).

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

Both fandango mutant alleles were isolated in the laboratory of Ruth Lehmann. We thank Kohtaro Tanaka for help with the in situs; our colleagues, Moises Mallo, Miguel Ferreira for discussion, and suggestions that greatly improved the manuscript; Jessica Thompson and Richard Hampson for manuscript editing. Proteins were identified at the Mass Spectrometry Laboratory Institute of Biochemistry and Biophysics Polish Academy of Science.

© 2014, Guilgur et al.

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