Caenorhabditis elegans SWI/SNF Subunits Control Sequential Developmental Stages in the Somatic Gonad

Abstract

The Caenorhabditis elegans somatic gonadal precursors (SGPs) are multipotent progenitors that give rise to all somatic tissues of the adult reproductive system. The hunchback and Ikaros-like gene ehn-3 is expressed specifically in SGPs and is required for their development into differentiated tissues of the somatic gonad. To find novel genes involved in SGP development, we used a weak allele of ehn-3 as the basis for a reverse genetic screen. Feeding RNAi was used to screen ∼2400 clones consisting of transcription factors, signaling components, and chromatin factors. The screen identified five members of the C. elegans SWI/SNF chromatin remodeling complex as genetic enhancers of ehn-3. We characterized alleles of 10 SWI/SNF genes and found that SWI/SNF subunits are required for viability and gonadogenesis. Two conserved SWI/SNF complexes, PBAF and BAF, are defined by their unique array of accessory subunits around a common enzymatic core that includes a catalytic Swi2/Snf2–type ATPase. Tissue-specific RNAi experiments suggest that C. elegans PBAF and BAF complexes control different processes during somatic gonadal development: PBRM-1, a signature subunit of PBAF, is important for normal SGP development, whereas LET-526, the distinguishing subunit of BAF, is required for development of a differentiated cell type, the distal tip cell (DTC). We found that the SWSN-4 ATPase subunit is required for SGP and DTC development. Finally, we provide evidence that C. elegans PBAF subunits and hnd-1/dHand are important for the cell fate decision between SGPs and their differentiated sisters, the head mesodermal cells.

One of the fundamental questions in developmental and stem cell biology is how a single progenitor cell can differentiate into multiple cell types, leading to tissue and organ development. The C. elegans somatic gonadal precursors (SGPs) are multipotent progenitors that develop into all somatic cells of the adult reproductive system. Two SGPs are generated during embryogenesis and, together with two primordial germ cells (PGCs), comprise the four-celled gonadal primordium (Sulston et al. 1983). In hermaphrodites, each SGP generates one of the two U-shape “arms” of the reproductive system via nearly identical and highly stereotyped cell lineages (Kimble and Hirsh 1979). In total, there are 143 cells and five mature tissues in the hermaphrodite somatic gonad, including distal tip cells (DTCs), an anchor cell (AC), sheath, spermatheca, and uterus (Hubbard and Greenstein 2000). We previously identified four transcriptional regulators that are expressed and function early in SGPs: the dHand gene hnd-1 is required for SGP survival (Mathies et al. 2003); the GLI ortholog tra-1 controls SGP polarity (Mathies et al. 2004); and two hunchback and Ikaros-like (HIL) genes, ehn-3 and R08E3.4/ztf-16, are required for the development of SGPs into differentiated cell types (Large and Mathies 2010). None of these genes appears to be required for the specification of SGPs and very little is known about the determinants of SGP potency. We used a sensitized RNAi screen to identify additional SGP regulators and found evidence that SWI/SNF chromatin remodeling complexes control early SGP development.

SWI/SNF complexes are large, multi-subunit complexes that utilize the energy of ATP hydrolysis to alter the interaction between nucleosomes and DNA, thereby affecting the accessibility of DNA and influencing gene expression (Clapier and Cairns 2009). In humans, the complexes are approximately 2 mDa in size, contain 8–11 subunits, and are encoded by at least 21 genes (Hargreaves and Crabtree 2011; Ho et al. 2009; Wu 2012). The overall subunit composition of the complexes is conserved across phyla; however, individual subunits are often encoded by more than one gene in mammals (Figure 1A). The enzymatic core consists of four subunits that have full chromatin remodeling activity in vitro (Phelan et al. 1999). Central to this activity is a Swi2/Snf2-type ATPase, BRM or BRG1 in mammals and Brahma in Drosophila. Mutation of the core subunits results in early lethality in mice and flies (Brizuela et al. 1994; Bultman et al. 2000; Crosby et al. 1999; Dingwall et al. 1995; Guidi et al. 2001; Kim et al. 2001; Klochendler-Yeivin et al. 2000; Roberts et al. 2000; Tamkun et al. 1992), underscoring the importance of SWI/SNF for development.

Figure 1.

C. elegans SWI/SNF chromatin remodeling complexes. The C. elegans genome contains homologs of all SWI/SNF subunits. We classified them as core (dark gray), accessory (light gray), or complex-specific (PBAF, blue; BAF, orange) based on the purified mammalian complexes. SWSN-9 is considered a potential BAF or PBAF subunit because of its similarity to BRD7 and BRD9, which are subunits of PBAF and BAF, respectively. (A) Mammalian, Drosophila, and C. elegans proteins are listed. Subunits identified in our ehn-3 enhancer screen are indicated with asterisks (*). (B) By analogy with mammalian SWI/SNF, the C. elegans subunits are predicted to combine to form molecularly and functionally distinct complexes. (C) C. elegans SWI/SNF proteins, including all major domains. Only the longest isoform is listed.

In addition to the enzymatic core, SWI/SNF complexes contain common and complex-specific accessory subunits (Figure 1A). Two major subfamilies of SWI/SNF, called Brg/Brm–associated factors (BAF) and Polybromo-BAF (PBAF), are distinguished by their unique accessory subunits. The homologous complexes in Drosophila are called BAP and PBAP. BAF/BAP complexes contain the ARID protein, BAF250a or BAF250b in mammals and Osa in Drosophila. PBAF/PBAP complexes contain two well-characterized subunits: the bromodomain protein BAF180 in mammals and Bap180/Polybromo in Drosophila and the ARID protein BAF200 in mammals and Bap170 in Drosophila (Chalkley et al. 2008; Kwon and Wagner 2007; Mohrmann and Verrijzer 2005). BAF/BAP and PBAF/PBAP have overlapping and distinct functions in mammalian gene regulation and Drosophila development (Gao et al. 2008; Huang et al. 2008; Lemon et al. 2001; Moshkin et al. 2007; Wang et al. 2004; Yan et al. 2005; Yan et al. 2008). These functional differences likely result from targeting of the two complexes to different chromosomal regions, as has been demonstrated in Drosophila (Mohrmann et al. 2004).

The in vivo roles of common accessory subunits are less well-characterized, but evidence to date suggests that they are important for the functional specificity of the complexes. For example, mammalian neural progenitors utilize a complex called npBAF that contains BAF45a and BAF53a, whereas differentiated neurons use a complex called nBAF that contains BAF45b and BAF53b (Lessard et al. 2007). The switch from npBAF to nBAF is essential for the cessation of proliferation and the differentiation of neuronal subtypes. Furthermore, BAF53a cannot substitute for BAF53b in neurons (Wu et al. 2007), suggesting that this accessory protein provides biological specificity to the complex. Therefore, specific combinations of accessory subunits play a key role in determining the functional diversity of SWI/SNF complexes.

C. elegans SWI/SNF genes were initially identified for their role in the asymmetric division of a tail hypodermal cell, the T cell (Sawa et al. 2000). They have since been identified as genetic regulators of larval development (Cui et al. 2004), the UV DNA damage response (Lans et al. 2010), hermaphrodite-specific neuron (HSN) development (Weinberg et al. 2013), and gonadogenesis (Shibata et al. 2012). More recently, proteomics approaches identified SWI/SNF subunits in association with two transcription factors, DAF-16 and SOMI-1 (Hayes et al. 2011; Riedel et al. 2013). Genetic, developmental, and proteomic analyses of predicted SWI/SNF subunits are beginning to reveal key similarities and differences between C. elegans SWI/SNF complexes and their mammalian counterparts.

Here, we characterized alleles of several C. elegans SWI/SNF subunits and found that they are broadly required for viability and act in parallel to ehn-3 in the somatic gonad. We used tissue-specific RNAi to examine the functions of predicted BAF and PBAF subunits and showed that they control distinct events during gonadogenesis. Finally, we found that genes encoding PBAF subunits have a mutant phenotype that is strikingly similar to that of hnd-1 mutants and provide evidence that hnd-1 and PBAF are important for distinguishing multipotent SGPs from their differentiated sisters.

Materials and Methods

Strains

C. elegans strains were cultured as described previously (Brenner 1974; Wood 1988). All strains were grown at 20° unless otherwise specified and were derived from the Bristol strain N2. The following mutations were used in this study and are described in C. elegans II (Hodgkin 1997), cited references, or the following work:

LGI: pbrm-1(tm415) (Shibata et al. 2012), pbrm-1(ok843), let-526(h185) (Johnsen et al. 2000), let-526(gk816), let-526(tm4795), swsn-2.2(ok3161) (Weinberg et al. 2013), swsn-2.2(tm3395), swsn-9(ok1354)

LGII: swsn-7(gk1041), swsn-7(tm4263), rrf-3(pk1426)

LGIII: ham-3/swsn-2.1(tm3309) (Weinberg et al. 2013), snfc-5/swsn-5(ok622) (Lans et al. 2010), swsn-3(tm3647)

LGIV: ehn-3(q766) (Mathies et al. 2004), ehn-3(rd2) (Large and Mathies 2010), psa-4/swsn-4(os13) (Sawa et al. 2000), psa-4/swsn-4(tm305)

LGV: psa-1/swsn-1(ku355) (Cui et al. 2004), psa-1/swsn-1(os22) (Sawa et al. 2000), psa-1/swsn-1(tm4567), rde-1(ne219) (Tabara et al. 1999), rol-9(sc148)

LGX: hnd-1(q740) (Mathies et al. 2003), ztf-16(tm2127) (Large and Mathies 2010)

The following balancer chromosomes and molecular markers were used in this study: hT2[bli-4(e937) let-?(q782) qIs48] for LGI and LGIII (referred to as hT2g), qC1[dpy-19(e1259) glp-1(q339) qIs26] and sC1[dpy-1(s2170)] for LGIII, mIn1[dpy-10(e128) mIs14] for LGII, and nT1[let-? qIs51] (referred to as nT1g) for LGIV and LGV, rdIs2 [ehn-3A::GFP] (Welchman et al. 2007), rdIs11 [ehn-3A::tdTomato], rdIs4 [ehn-3A::Venus], ccIs4444 [arg-1::GFP] (Kostas and Fire 2002).

Regulome RNAi screen

We compiled a set of ∼2400 RNAi clones consisting of transcription factors, cell signaling components, and chromatin factors from two commercially available genome-wide RNAi libraries, the C. elegans ORF-RNAi library (Source BioScience, Nottingham, UK) (Rual et al. 2004) and the C. elegans RNAi library (Source BioScience, Nottingham, UK) (Kamath et al. 2003). Our “regulome” sublibrary included the published signal transduction, transcriptional regulation, and chromatin remodeling libraries (Reece-Hoyes et al. 2005), chromatin factors described in WormBook (Cui and Han 2007), and the Ahringer chromatin, phosphatase, and transcription factor libraries (Source BioScience, Nottingham, UK). Feeding RNAi was performed essentially as reported by Kamath et al. (2003). Briefly, L4 worms fed on RNAi bacteria for 24 hr, were transferred in duplicate to new wells seeded with RNAi bacteria, and gravid adult worms were allowed to lay eggs for a 24-hr period. The ehn-3(q766) worms were screened in parallel to N2 in adjacent columns of a 12-well plate. Defects in gonadal morphology were assessed in the F1 generation using a dissecting microscope. At least 50 animals were examined per well and the penetrance was recorded. We scored as positive any clones that resulted in more than 10% gonadogenesis defects in either the wild-type or ehn-3(q766) background. All RNAi clones that gave similar results in a secondary screen were sequenced to verify the clone identity.

Identification and classification of C. elegans SWI/SNF genes

Potential C. elegans SWI/SNF genes were identified using a combination of BLAST searches, OrthoList, and previously published articles (Altschul et al. 1997, 2005; Cui et al. 2004; Sawa et al. 2000; Shaye and Greenwald 2011; Shibata et al. 2012; Wu et al. 2009; Yoo and Crabtree 2009). For subunits with more than one C. elegans homolog, we used sequence alignments and protein domain architecture to identify the most likely ortholog(s). Sequences were aligned using Clustal Omega (Sievers et al. 2011) in Jalview 2.8 (Waterhouse et al. 2009). The results are summarized in Suppporting Information, File S1. Two C. elegans genes, psa-4/swsn-4 and C52B9.8, encode proteins with significant sequence similarity to human BRM and BRG1. SWSN-4 had been previously described as a C. elegans SWI/SNF subunit (Cui et al. 2004; Sawa et al. 2000). SWSN-4 contains all seven domains found in human BRM/BRG1, whereas C52B9.8 contains only the HSA, SNF2, and Helicase C domains (File S1). RNAi knockdown of C52B9.8 did not affect viability or gonadogenesis (data not shown); whether or not C52B9.8 retains overlapping functions with swsn-4 remains to be determined. Two genes, swsn-2.1/ham-3 and swsn-2.2, encode proteins with sequence similarity to mammalian BAF60 proteins. The C. elegans proteins are not clear orthologs of any specific BAF60 protein; instead, the worm and mammalian genes appear to have duplicated independently (Weinberg et al. 2013). Two genes, phf-10 and dpff-1, encode proteins with sequence similarity to mammalian BAF45 proteins. C. elegans PHF-10 is most closely related to BAF45a/PHF10, whereas DPFF-1 is equally similar to BAF45b, c, and d (also known as DPF1-3). The DPF proteins all contain an N-terminal Requiem domain that is not present in PHF10 (File S1). RNAi knockdown of phf-10 resulted in gonadogenesis defects that were stronger in the ehn-3(q766) background, whereas RNAi of dpff-1 did not affect viability or gonadogenesis (data not shown). We classified PHF-10 and DPFF-1 as common accessory subunits in accordance with previous publications; however there is some evidence to suggest that human BAF45a/PHF10 may be predominantly found in PBAF complexes, whereas BAF45b/c/d (DPF1-3) are found in BAF complexes (Middeljans et al. 2012). Finally, C. elegans has a single protein, SWSN-9, with similarity to mammalian BRD7 and BRD9. Human BRD7 and BRD9 have 27.1% and 23.0% amino acid identity with SWSN-9, respectively, compared to 36.7% shared amino acid identity between the human proteins. To clarify the relationship between SWSN-9 and the mammalian proteins, we constructed a phylogenetic tree using maximum likelihood and maximum parsimony analysis in Mega 5.2.2 (Tamura et al. 2011). BRD7/9 genes were identified using BLAST searches with the human BRD7 and BRD9 proteins (File S1). C. elegans SWSN-9 is not an obvious ortholog of mammalian BRD7 or BRD9; instead, the ancestral BRD7/9 protein appears to have duplicated in vertebrates (Figure S3).

Genetic and molecular analysis of SWI/SNF alleles

SWI/SNF alleles used in this study are listed in Table 1. Deletion alleles obtained from the International C. elegans Gene Knockout Consortium or National BioResource Project were crossed alternately to N2 and an appropriate balancer chromosome at least three times (a total of six outcrosses), and the breakpoint was sequenced to verify the molecular lesion (Table S1 and Figure S1). Complementation tests were performed for genes with more than one allele: swsn-1(tm4567) failed to complement swsn-1(os22) at 25°; swsn-2.2(tm3395) failed to complement swsn-2.2(ok3161); swsn-4(tm305) failed to complement swsn-4(os13) at 25°; swsn-7(gk1041) failed to complement swsn-7(tm4263); pbrm-1(ok843) failed to complement pbrm-1(tm415); and let-526(tm4795) and let-526(gk816) failed to complement let-526(h185). These results suggest that the observed phenotypes are attributable to the deletions and not to linked mutations.

Table 1. Alleles used in this study.

Gene	Allele	Mutation	Affect on Locus	Potential Null
swsn-1/psa-1	os22	Missense	P86S	No
	ku355	Missense	P86L	No
	tm4567	Insertion/deletion	Frame shift after E60	Yes
swsn-2.1	tm3309	Insertion/deletion	Frame shift after V67	Yes
swsn-2.2	tm3395	Deletion	Frame shift after K65	Yes
	ok3161	Deletion	Frame shift after I62	Yes
swsn-3	tm3647	Insertion/deletion	Promoter/start deletion	Noa
swsn-4/psa-4	os13	Missense	T673I L697F	No
	tm305	Deletion	Frame shift after G630	Yes
swsn-5	ok622	Deletion/duplication	Unknown	Noa
swsn-7	gk1041	Deletion	Frame shift after A189	Yes
	tm4263	Deletion	Deletion of R40 – W406	Yes
swsn-9	ok1354	Deletion	Frame shift after I197	Yes
pbrm-1	ok843	Deletion	Frame shift after I390	Yesb
	tm415	Insertion/deletion	Frame shift after L539	Yesb
let-526	h185	Nonsense	Q473stop	Yes
	gk816	Insertion/deletion	Frame shift after R47	Yes
	tm4795	Deletion	Frame shift after A1248	Yes

^aSee Figure S2.

^bDeletion affects pbrm-1a; pbrm-1b may be unaffected.

The swsn-5(ok622) and swsn-3(tm3647) deletion alleles did not display phenotypes observed in previous RNAi experiments (Kamath et al. 2003; Rual et al. 2004; Sawa et al. 2000); therefore, we outcrossed the strains further and analyzed them molecularly. PCR from genomic DNA or single-stranded cDNA was used to detect duplication events or transcripts corresponding to the locus, respectively. For RT-PCR, mixed stage worms were washed from nearly starved plates and RNA was prepared using TRIzol (Invitrogen). First strand cDNA was synthesized using Superscript II (Invitrogen) and oligo dT. For genomic PCR, mixed stage worms were treated with proteinase K and used directly as template. PCR assays failed to detect an additional copy of swsn-3 in the swsn-3(tm3647) deletion strain. However, RT-PCR indicated that the 3′ end of the locus was expressed in swsn-3(tm3647) homozygotes (Figure S2); therefore, tm3647 may retain some activity. PCR and RT-PCR revealed that the swsn-5 coding region is present and expressed in swsn-5(ok622) homozygotes (Figure S2), indicating that this strain contains a secondary duplication of the locus.

Phenotypic analysis

Three to 12 (depending on viability) young adults were placed on each of three plates and allowed to lay eggs for 24 hr. Gonadogenesis defects were assessed in the F1 generation at the fourth larval stage using a dissecting microscope; the number of worms with missing gonadal arms, disorganized gonads, or no visible gonad were recorded. The average penetrance and SD of these gonadogenesis defects were calculated. The frequency of missing anterior gonadal arms was calculated relative to the number of worms with one missing arm. Unpaired t-tests were used for pairwise statistical comparisons and the raw p-value is reported.

Tissue-restricted RNAi

The mesodermal RNAi strain was generated by cloning rde-1 genomic sequence, including all exons, introns, and UTRs, downstream of the hnd-1 promoter from pJK848 (Mathies et al. 2003). The resulting plasmid, pRA279, was injected into rrf-3(pk1426); unc-119(ed3); rde-1(ne219) with an unc-119 rescue construct as a co-injection marker (Maduro and Pilgrim 1995) and integrated with gamma irradiation to create rdIs7[hnd-1::rde-1]. The strain was backcrossed to unc-119(ed3); rde-1(ne219) and the rrf-3 mutation was removed. RNAi was performed by injection of double-stranded RNA (dsRNA) into the gonad. dsRNA was synthesized using the Megascript T7 kit (Ambion) and injected at 0.2–1 mg/ml. In each case, the template contained at least 500 bp of coding sequence. Available RNAi clones were used as template for swsn-1, pbrm-1, and let-526 (Kamath et al. 2003; Rual et al. 2004). The swsn-4 RNAi clone was generated by amplifying 1680 bp of swsn-4 genomic sequence with primers RA714/RA715 (Table S2) using a two-step PCR protocol to add T7 promoter sequence and restriction sites for cloning (Dudley and Goldstein 2005).

Reporter constructs

ehn-3A::Venus (pRA264) was created by amplifying the ehn-3A promoter and 5′UTR from pRA230 using primers RA291/RA314 (Table S2) and cloning the XbaI to BamHI fragment into the pPD95.77 expression vector containing the Venus variant of GFP. This construct was then truncated at a BglII site, retaining 948 bp upstream of the ehn-3A ATG. ehn-3A::tdTomato (pRA351) was generated by cloning the BglII to BamHI fragment of pRA230 into the pPD95.77 expression vector containing tdTomato; this construct retains 948 bp upstream of the ehn-3A ATG to the PstI site in the second ehn-3A exon. pRA255 and pRA351 were injected into unc-119(ed3); him-5(e1490) with an unc-119 rescue construct as a co-injection marker (Maduro and Pilgrim 1995) and integrated by gamma irradiation to create rdIs4 [ehn-3A::Venus] and rdIs11 [ehn-3A::tdTomato]. Reporters were visualized using a Zeiss Axioskop II or Zeiss LSM710 microscope.

Results

The reproductive system develops from a four-celled primordium containing two SGPs and two PGCs. SGPs are generated during embryogenesis from mesodermal lineages (Sulston et al. 1983) and remain quiescent until the larval stages, when they undergo several rounds of cell division to generate all 143 cells of the adult hermaphrodite gonad (Kimble and Hirsh 1979). Of particular importance are two DTCs, which are critical for generating the proper morphology and maintaining the function of the reproductive system. DTCs guide the elongation of the two gonadal “arms” to produce the U-shape hermaphrodite gonad and they provide a signal to the adjacent germ cells to promote their mitotic proliferation (Kimble and White 1981). The C. elegans hunchback and Ikaros-like gene, ehn-3, is expressed specifically in SGPs and is important for the development of several differentiated tissues of the somatic gonad, including DTCs (Large and Mathies 2010; Mathies et al. 2004). Despite the importance of ehn-3 for gonadogenesis, it is not known how this zinc finger transcription factor acts in SGPs to control their subsequent development.

To learn more about how ehn-3 controls SGP development and to identify new SGP regulators, we used a weak allele of ehn-3 to provide a sensitized background for an RNAi screen. ehn-3(q766) mutants have a low penetrance of missing gonadal arms and this phenotype is strongly enhanced by reducing the function of other SGP regulators, such as hnd-1 and tra-1 (Mathies et al. 2003, 2004). We limited our screen to genes involved in transcriptional regulation, including transcription factors, signaling components, and chromatin factors (see Materials and Methods). We used feeding RNAi and we screened L4 larvae for gross defects in gonadal morphology using a dissecting microscope. Positives from the primary screen were retested and the clones were sequenced to verify their identity. From a screen of ∼2400 genes, we identified 33 ehn-3 enhancers (File S2). Among these were five members of the C. elegans SWI/SNF chromatin remodeling complex. This result was intriguing in light of the functional similarities between ehn-3 and Ikaros (Large and Mathies 2010) and the physical interaction between Ikaros and SWI/SNF in mammalian lymphocytes (Kim et al. 1999; O’Neill et al. 2000). Therefore, we focused on defining the role(s) of SWI/SNF complexes in somatic gonad development.

C. elegans SWI/SNF

The C. elegans genome encodes homologs of all mammalian SWI/SNF subunits (see Materials and Methods) (Figure 1). SWI/SNF complexes have not been biochemically purified in C. elegans; therefore, we used the mammalian complexes as a framework for our genetic analysis (Figure 1B) (Ho et al. 2009; Wang et al. 1996a, 1996b). Accordingly, we expect that distinct BAF and PBAF complexes will be defined by their unique accessory subunits, with BAF containing LET-526/BAF250 and PBAF containing PBRM-1/BAF180 and SWSN-7/BAF200. SWSN-9 is the single C. elegans homolog of mammalian BRD7 and BRD9 (Figure S3). Because BRD7 is found in PBAF, whereas BRD9 is found in BAF (Kadoch et al. 2013; Kaeser et al. 2008; Middeljans et al. 2012), we included SWSN-9 as a potential BAF or PBAF subunit. Finally, we considered that functional diversity might result from the utilization of different paralogs of the accessory proteins, BAF60 (SWSN-2.1 and SWSN-2.2) and BAF45 (PHF-10 and DPFF-1), as has been proposed for mammalian BAF complexes (Ho and Crabtree 2010). Alleles exist for many of the C. elegans SWI/SNF genes (Table 1); however, only a few have been characterized genetically (Cui et al. 2004; Lans et al. 2010; Sawa et al. 2000; Shibata et al. 2012; Weinberg et al. 2013).

Consistent with a broad role in development, we found that many of the SWI/SNF subunits are required for embryonic or larval viability. We began with deletion alleles of the core genes, swsn-1, swsn-4, and swsn-5. We found that swsn-1(tm4567) homozygotes were larval lethal and swsn-4(tm305) homozygotes were embryonic lethal (Table 2). Temperature-sensitive alleles of swsn-1 and swsn-4 are embryonic lethal at the restrictive temperature (Cui et al. 2004; Sawa et al. 2000); therefore, our results indicate that swsn-1 has a maternal contribution that is necessary for embryogenesis. Unlike swsn-1 and swsn-4 deletions, the swsn-5(ok622) deletion was homozygous viable and displayed no maternal effect lethality (n = 1125). This deletion was hypersensitive to UV damage, as were temperature-sensitive alleles of swsn-1 and swsn-4 (Lans et al. 2010). However, our molecular analysis showed evidence for a secondary duplication of the locus in swsn-5(ok622) homozygotes (Figure S2). Because swsn-5 RNAi results in embryonic lethality (E. E. Large and L. D. Mathies, unpublished observations; Sawa et al. 2000), we conclude that ok622 is not a strong loss-of-function allele. We also examined alleles of the accessory genes, swsn-2.1, swsn-2.2, and swsn-3. Deletion alleles of swsn-2.1 or swsn-2.2 were homozygous viable, but they exhibited highly penetrant maternal effect lethality (Table 2). A recent article described distinct functions for swsn-2.1 and swsn-2.2 in the hermaphrodite specific neurons (Weinberg et al. 2013). To determine whether these genes retain overlapping functions, we generated a balanced strain containing swsn-2.1(tm3309) and swsn-2.2(ok3161). Double mutants derived from this strain did not survive beyond the L2 larval stage, indicating that swsn-2.1 and swsn-2.2 are redundant for embryonic or early larval development. Finally, we found that a swsn-3 deletion allele was homozygous viable and displayed no maternal effect lethality (n = 576). Molecular analysis indicates that swsn-3(tm3647) contains mRNA that could produce a protein lacking the HMG domain but retaining the conserved NHRLI domain (Figure S2). Experiments with the Drosophila homolog of swsn-3, Bap111, indicate that sequences outside of the HMG domain may be important for its function (Papoulas et al. 2001). Therefore, it is likely that swsn-3(tm3647) retains some gene activity. In summary, our genetic analysis implicates SWI/SNF core (swsn-4 and swsn-1) and accessory (swsn-2.1 and swsn-2.2) subunits in embryonic or larval development.

Table 2. Embryonic and larval lethality of SWI/SNF alleles.

Parental Genotypea	Embryonic Lethality %b	Larval Lethality %b	n
swsn-1(tm4567)/+	2.5	26.8	276
swsn-2.1(tm3309)	41.3	24.2	256
swsn-2.2(tm3395)	77.5	19.7	806
swsn-2.2(ok3161)	85.9	10.7	347
swsn-4(tm305)/+	28.9	2.2	277
swsn-7(tm4263)	100	0	454
swsn-7(gk1041)	100	0	189
swsn-9(ok1354)	6.5	42.7	651
pbrm-1(ok843)	2.6	96.0	623
pbrm-1(tm415)	1.3	20.9	949
let-526(gk816)/+	0.8	26.6	237

^aAlleles were backcrossed before analysis; however, linked mutations may still be present.

^bEmbryonic and larval lethality were assessed using a dissecting microscope and are reported as a percentage of the total progeny (n).

Next, we examined alleles of predicted BAF and PBAF genes (Figure 1A). We found that let-526(gk816) and let-526(tm4795) homozygotes died as early larvae (Table 2; data not shown), similar to previously characterized alleles of let-526 (Shibata et al. 2012). Deletion alleles of pbrm-1 are homozygous viable and resulted in maternal effect larval lethality (Table 2). The two pbrm-1 alleles differ in their phenotypic severity: pbrm-1(ok843) was mostly larval lethal, whereas pbrm-1(tm415) had a higher percentage of viable progeny. The pbrm-1(ok843) and pbrm-1(tm415) deletion alleles express mRNAs encoding proteins that are truncated after the second or third bromodomains, respectively. Therefore, pbrm-1(ok843) is a stronger loss-of-function allele by molecular and genetic criteria. Both alleles of swsn-7 were homozygous viable and resulted in 100% maternal effect embryonic lethality (Table 2). Therefore, two PBAF genes, swsn-7 and pbrm-1, have different terminal phenotypes. Finally, we examined the function of swsn-9, which is a potential BAF or PBAF gene. The swsn-9(ok1354) deletion allele was viable and resulted in partial maternal effect larval lethality, similar to pbrm-1 alleles. We conclude that BAF and PBAF genes are required for viability and specific subunits appear to play distinct roles in early development.

Finally, we investigated the requirement for SWI/SNF in the somatic gonad. To do this, we examined viable SWI/SNF alleles for defects in gonadal morphology using a dissecting microscope (Figure 2A, white bars; Table S3). Temperature-sensitive alleles of swsn-1 and swsn-4 had a low penetrance of missing gonadal arms, as has been previously reported (Cui et al. 2004; Shibata et al. 2012). We found that swsn-1 and swsn-4 deletion heterozygotes were occasionally missing one of the two gonadal arms, suggesting that SWI/SNF has dose-sensitive functions in the somatic gonad. Similarly, the surviving progeny of swsn-2.1 or swsn-2.2 homozygotes were sometimes missing gonadal arms. Because swsn-2.1 and swsn-2.2 are paralogs, this may reflect a dose-sensitive requirement for C. elegans BAF60 in gonadogenesis. Finally, pbrm-1 and swsn-9 mutants had gonadogenesis defects that were more severe in the progeny of deletion homozygotes, indicating that they are required maternally and zygotically for gonadogenesis. In summary, we find that at least six SWI/SNF subunits, including the SWSN-4 ATPase, have functions in somatic gonad development.

Figure 2.

C. elegans subunits act alone and in parallel to ehn-3 in the somatic gonad. (A) SWI/SNF mutants have gonadogenesis defects alone or in combination with ehn-3(rd2). Genotype is indicated on the left; maternal [m+ or m−] and zygotic [z+ or z−] contributions are indicated when relevant. Percentages of animals with gonadogenesis defects in an otherwise wild-type (white bars) or ehn-3(rd2) background (black bars) are shown. Unpaired t-tests were used for statistical comparisons; ehn-3(rd2) was compared and the significance is reported (NS, not significant; *P ≤0.05; ***P ≤ 0.001). NT indicates double mutant combinations that were not tested. Additional data are found in Table S3. (B–E) DIC images showing the range of gonadogenesis defects seen in pbrm-1(ok843); ehn-3(rd2) double mutants. (B) Missing anterior gonadal arm (posterior is seen), (C) unextended gonad with a clear patch of gonadal tissue, or (D, E) severely reduced gonad. Dashed lines and arrowheads indicate gonadal tissue; carats point to the vulva when present.

SWI/SNF genes act in parallel to ehn-3

To ask how the SWI/SNF complex interacts with ehn-3, we generated double mutants using a null allele of ehn-3. We found that alleles of swsn-1, swsn-2.1, swsn-2.2, swsn-7, swsn-9, and pbrm-1 strongly enhanced the ehn-3(rd2) phenotype (Figure 2A, black bars; Table S3). Importantly, the penetrance and severity of the defects were greater in double homozygotes when compared to the relevant single mutants (Table S4). This is exemplified by the interaction between ehn-3(rd2) and pbrm-1(ok843). Wild-type worms have two U-shape gonadal arms centered on the vulva (Kimble and White 1981), whereas ehn-3(rd2) and pbrm-1(ok843) single mutants were occasionally missing one of the two gonadal arms (Large and Mathies 2010) (Table S4). In contrast, pbrm-1(ok843); ehn-3(rd2) double mutants were frequently missing one or both gonadal arms (Figure 2, B and C) and they often had severely reduced gonads (Figure 2, D and E). This severe phenotype was almost never observed in ehn-3(rd2) or pbrm-1(ok843) single mutants. We conclude that a SWI/SNF complex acts in parallel to ehn-3 in the somatic gonad. Because both PBAF genes interacted strongly with ehn-3, this suggests that the complex acting in parallel to ehn-3 is PBAF.

Distinct functions for PBAF and BAF subunits in the somatic gonad

To clarify the roles of specific SWI/SNF subunits in somatic gonad development, we used a tissue-specific RNAi strategy to circumvent the embryonic and larval lethality associated with the loss of SWI/SNF function. This approach uses lineage-restricted promoters to drive expression of rde-1 in rde-1 (RNAi-deficient) mutants, thus rescuing RNAi in these lineages (Qadota et al. 2007). We used the hnd-1 promoter, which is expressed broadly in the MS, C, and D lineages and later in SGPs (Mathies et al. 2003). These lineages produce predominantly mesodermal cell types; therefore, we refer to this treatment as mesodermal RNAi. We used swsn-4, pbrm-1, and let-526 as representative core, PBAF, and BAF genes, respectively. All three genes produced strong RNAi phenotypes, as evidenced by nearly complete embryonic or larval lethality in a wild-type background and gonadogenesis defects in the mesodermal RNAi background (Table S5). The penetrance of gonadal defects was lower for pbrm-1 RNAi than for swsn-4 and let-526 RNAi, but it was similar to pbrm-1 deletion alleles. Qualitatively, swsn-4 and let-526 RNAi resulted in a centrally located patch of gonadal tissue with no arm elongation, whereas pbrm-1 RNAi resulted in missing gonadal arms. Therefore, mesoderm-restricted RNAi reveals strong and distinct functions for specific SWI/SNF subunits.

To elucidate the developmental processes controlled by specific SWI/SNF subunits, we built molecular markers into the mesodermal RNAi strain. We used ehn-3A::Venus to mark SGPs at the L1 stage and lag-2::GFP to mark DTCs at the L4 stage (Siegfried et al. 2004). We began by examining L1 larvae for the presence and position of the SGPs. Wild-type worms have two SGPs located at the poles of the gonadal primordium (Kimble and Hirsh 1979). Similarly, SGPs were almost always present at the poles of the primordium in let-526 RNAi (Figure 3B). By contrast, SGPs were sometimes absent or misplaced within the primordium in pbrm-1 and swsn-4 RNAi (Figure 3, C–E). Therefore, swsn-4 and pbrm-1, but not let-526, are required for the presence and positioning of SGPs.

Figure 3.

SWI/SNF subunits have distinct phenotypes in the somatic gonad. RNAi was performed in the mesodermal RNAi strain with markers for SGPs (ehn-3A::Venus) and DTCs (lag-2::GFP). The gene knockdown is indicated. (A) Percentage of worms (n) with each observed phenotype. Missing and misplaced SGPs (gray bars) were identified using ehn-3A::Venus; missing DTCs (black bars) and non-DTCs expressing lag-2::GFP (green bars) were identified using lag-2::GFP. Representative images are shown in (B–H). (B–E) DIC (left), fluorescence (center), and overlaid images (right) of L1 larvae expressing ehn-3A::Venus in SGPs. Two SGPs were present at the poles of the primordium in wild-type and let-526 RNAi (B). SGPs were sometimes missing (C, E) or could be located more centrally within the primordium (D) in pbrm-1 and swsn-4 RNAi. (F–H) Overlaid fluorescence and DIC images of L4 larvae expressing lag-2::GFP. Wild-type worms express lag-2::GFP brightly in two crescent-shape DTCs located at the ends of the gonadal arms. DTCs were missing in pbrm-1, swsn-4, and let-526 RNAi and additional gonadal cells expressing lag-2::GFP (non-DTCs) were observed in swsn-4 and let-526 RNAi. (F) The anterior arm was present and contained a DTC with typical morphology (black arrowhead); the posterior arm was absent (not shown). (G, H) No DTCs were present; however, lag-2::GFP–expressing cells were seen in the gonad (white arrowheads). The vulva (carat) also contained cells expressing lag-2::GFP, which were evident in longer exposures (G, H). Fluorescence exposures were 200 ms (B–E), 1 ms (F), and 10 ms (G, H).

The hermaphrodite DTCs have at least two functions: to lead migration of the two gonadal arms and to promote mitotic proliferation in the germline (Kimble and Hirsh 1979; Kimble and White 1981). Wild-type worms have one DTC at the end of each gonadal arm. We found that pbrm-1, swsn-4, and let-526 RNAi all resulted in missing DTCs (Figure 3A); however, they appeared to affect different developmental processes. pbrm-1 RNAi resulted in occasional missing DTCs that correlated with missing gonadal arms. When DTCs were present, they had typical morphology and were located at the end of elongated gonadal arms (Figure 3F). Furthermore, the percentage of worms with missing SGPs was approximately the same as the percentage of worms with missing DTCs, suggesting that missing DTCs are a secondary consequence of missing SGPs. By contrast, swsn-4 and let-526 RNAi often resulted in unextended gonads that lacked normal DTCs but nonetheless contained cells expressing lag-2::GFP (Figure 3, G and H). These cells expressed lag-2::GFP at a lower level, they did not have the typical crescent-shape of DTCs, and they did not lead migration of the gonadal arms. Therefore, they did not appear to be normal DTCs. We conclude that swsn-4 and let-526 are required for DTC formation and/or function.

In summary, we found that pbrm-1 RNAi resulted in missing and misplaced SGPs with a concomitant loss of DTCs, whereas let-526 RNAi resulted in missing DTCs with no effect on SGPs. Furthermore, swsn-4 RNAi resulted in missing and misplaced SGPs and a higher percentage of missing DTCs, indicating that the swsn-4 phenotype is an aggregate of the let-526 and pbrm-1 phenotypes. These observations are consistent with the idea that the SWSN-4 ATPase acts with PBRM-1 to control SGP development and LET-526 to control DTC development in the somatic gonad.

A common hnd-1 and PBAF phenotype

During the course of this work, we noticed that SWI/SNF mutants exhibited two phenotypes typical of hnd-1 mutants. First, swsn-4 and pbrm-1 RNAi resulted in missing or misplaced SGPs, as seen in hnd-1 mutants (Mathies et al. 2003). Second, SWI/SNF and hnd-1 mutants showed a bias toward missing anterior gonadal arms (Figure 4A). These phenotypes were not seen in other mutants affecting SGP development, such as ehn-3(rd2) and ehn-3(rd2); ztf-16(tm2127), suggesting that hnd-1 and PBAF might control a common process.

Figure 4.

SGPs have a mixed fate in hnd-1 mutants. (A) hnd-1 and SWI/SNF mutants are more likely to be missing the anterior gonadal arm. The percentage of missing anterior gonadal arms (relative to the total number of missing arms, n) is reported. Unpaired t-tests were used for statistical comparisons; ehn-3(rd2) was compared and the significance is indicated (*P ≤ 0.05; **P ≤ 0.01; ***P ≤ 0.001). (B) SGPs (Z1/Z4) and head mesodermal cells (hmcL/R) are sisters. hmcR dies by programmed cell death (x), whereas hmcL differentiates as the single hmc. (C–E) Overlaid DIC and fluorescence images showing ehn-3::tdTomato (red) and arg-1::GFP (green) expression in L1 larvae. (D, E) Higher-magnification views of SGPs are shown with fluorescent channels displayed separately (red′, green′′). (C, D) Wild-type worms express ehn-3::tdTomato in SGPs (D′) and arg-1::GFP in the hmc and tail neurons. (E) hnd-1 mutants often express arg-1::GFP in one or both SGPs (E′′); these SGPs also express ehn-3::tdTomato (E′). The hmc in hnd-1 mutants only expresses arg-1::GFP (not shown).

Each gonadal arm develops from one of two SGPs that sit at opposite poles of the gonadal primordium. The anterior SGP (Z1) generates the anterior gonadal arm and the posterior SGP (Z4) generates the posterior gonadal arm (Kimble and Hirsh 1979). To ask if Z1 and Z4 are differentially affected in hnd-1 mutants, we examined L1 larvae using ehn-3A::GFP to mark SGPs (Welchman et al. 2007). We found that hnd-1(q740) mutants were frequently missing one or both SGPs and the missing SGP was twice as likely to be Z1 (66.7%; n = 48). Therefore, differences between Z1 and Z4 are evident at the L1 stage in hnd-1 mutants and could account for the higher percentage of missing anterior gonadal arms. The sisters of Z1 and Z4 have different fates: the sister of Z1 is hmcR, which undergoes programmed cell death, whereas the sister of Z4 is hmcL, which differentiates as the single head mesodermal cell (Figure 4B) (Sulston et al. 1983). We reasoned that defects in the cell fate decision between SGPs and their sisters might explain the higher percentage of missing Z1 cells in hnd-1 mutants. To explore this, we examined hnd-1 mutants using ehn-3A::tdTomato to mark SGPs and arg-1::GFP to mark hmcs (Kostas and Fire 2002). In wild-type L1 larvae, arg-1::GFP is expressed in the hmc and cells in the tail, whereas ehn-3A::tdTomato is expressed in the two SGPs (Figure 4, C and D). In hnd-1 mutants, we often observed arg-1::GFP in one or both SGPs, and its expression could be very bright (Figure 4E). These SGPs also expressed ehn-3A::tdTomato and were associated with the primordial germ cells. Therefore, hnd-1 SGPs express reporters typical of SGPs and hmcs at the L1 larval stage. Because hnd-1 mutants always had two SGPs in embryos (Mathies et al. 2003), this suggests that hnd-1 is important for SGP cell fate determination or maintenance.

We asked if SWI/SNF mutants also express arg-1::GFP in SGPs. In wild-type larvae, arg-1::GFP is expressed only rarely and at very low levels in SGPs (Figure 5A). In contrast, swsn-1(os22), swsn-4(RNAi), and pbrm-1(ok843) frequently had strong expression of arg-1::GFP in one or both SGPs (Figure 5B–E). This suggests that hnd-1 and PBAF subunits are both important for SGP cell fate determination. Finally, let-526(RNAi) did not result in arg-1::GFP expression in SGPs (Figure 5E), consistent with the idea BAF and PBAF subunits have different functions in the somatic gonad.

Figure 5.

SWI/SNF mutants express arg-1::GFP in SGPs. DIC (A–D), fluorescence (A′–D′), and overlaid images (A′′–D′′) showing arg-1::GFP expression in SGPs. (A) Wild-type L1s occasionally expressed low levels of arg-1::GFP in SGPs. The exposure in (A′) is 500 ms compared to 100–200 ms in (B′–D′). (B) swsn-1(os22), (C), swsn-4(RNAi), and (D) pbrm-1(ok843) sometimes expressed arg-1::GFP in SGPs. (E) The percentage of animals with expression of arg-1::GFP in one or two SGPs is indicated. swsn-4 and let-526 RNAi were performed in the mesodermal RNAi strain.

Relationship between SWI/SNF and hnd-1

We previously demonstrated that hnd-1 acts in parallel to ehn-3 (Mathies et al. 2003), and here we show that SWI/SNF genes act in parallel to ehn-3. Shibata et al. (2012) reported that pbrm-1 mutants have reduced hnd-1::GFP expression in SGPs. Therefore, SWI/SNF may act in parallel to ehn-3 simply by virtue of its regulation of hnd-1. We used genetic epistasis analysis to ask if hnd-1 and pbrm-1 act in a simple linear pathway. To do this, we generated pbrm-1(tm415); hnd-1(q740) double mutants and examined them for gonadogenesis defects. The q740 deletion is a null allele; therefore, if pbrm-1 acts in the same pathway as hnd-1, then we expect the double mutant to resemble hnd-1(q740). We used pbrm-1(tm415) for this analysis because it had only minor gonadogenesis defects when derived from a heterozygous parent (4.2 ± 1.2%; n = 213). We found that pbrm-1(tm415); hnd-1(q740) double mutants had a significantly higher percentage of gonadogenesis defects (91.4 ± 6.5%; n = 58) when compared to hnd-1(q740) single mutants (50.0 ± 1.8%; n = 392; P = 0.01). We conclude that pbrm-1 acts upstream of and in parallel to hnd-1.

Discussion

In this study, we characterized alleles of 10 of the 13 C. elegans SWI/SNF subunits, laying the groundwork for future studies of the specific roles of individual subunits. Strong loss-of-function alleles of most SWI/SNF subunits were embryonic or larval lethal, indicating that SWI/SNF has important functions in early development. We defined different functions for SWI/SNF subunits in the somatic gonad: PBAF subunits are important for SGP development and act in parallel to ehn-3, whereas BAF subunits are required for DTC development. Finally, we described a common phenotype for hnd-1 and PBAF mutants and suggest that this phenotype results from defects in the determination and/or maintenance of the SGP fate.

PBAF subunits have unique developmental functions

We used a sensitized genetic background to examine the function(s) of SWI/SNF subunits in the somatic gonad. In total, six SWI/SNF genes interacted genetically with ehn-3, including alleles of core, accessory, and PBAF genes. Importantly, deletion alleles affecting homologs of two well-characterized PBAF subunits, PBRM-1/BAF180 and SWSN-7/BAF200, both strongly enhanced the ehn-3 phenotype. This suggests that a PBAF complex acts in parallel to ehn-3 in the somatic gonad. By contrast, SWSN-7 and PBRM-1 appear to perform different functions in early development: swsn-7 mutants arrest at the comma stage of embryogenesis, whereas pbrm-1 mutants arrest predominantly at the L1 larval stage. We used strong loss-of-function alleles and we compared the phenotypes resulting from loss of maternal and zygotic gene activity. Therefore, our data indicate that swsn-7 and pbrm-1 have similar functions in gonadogenesis and distinct functions in early development. This suggests that PBRM-1 and SWSN-7 are not dedicated subunits of the PBAF complex, but converge to form a PBAF complex during somatic gonadal development. The Drosophila homologs of these subunits, Bap170 and Bap180, have distinct and redundant functions in development (Carrera et al. 2008), and the mammalian homolog of PBRM-1, BAF180, is present in a high-molecular-weight complex that fractionates independently of PBAF (Lessard et al. 2007). Therefore, it is clear that PBAF subunits have additional functions that are independent of the PBAF complex. Genetic and biochemical analyses of PBAF subunits in model organisms will continue to reveal these novel functions and may also identify additional components of the PBAF complex.

Comparison of vertebrate and invertebrate SWI/SNF complexes

Vertebrate SWI/SNF complexes are known to utilize accessory subunits encoded by duplicate genes as a mechanism to generate functional diversity (Lessard and Crabtree 2010; Wu et al. 2009). For example, different BAF60 proteins have been implicated in mammalian embryonic stem cell pluripotency and self-renewal, heart development, and the establishment of left–right asymmetry (Ho et al. 2009; Lickert et al. 2004; Takeuchi and Bruneau 2009; Takeuchi et al. 2007). The C. elegans genome contains two genes, swsn-2.1 and swsn-2.2, encoding orthologs of the mammalian BAF60 proteins. A recent study found that swsn-2.1, but not swsn-2.2, was required for migration and serotonin production in the hermaphrodite-specific neurons (Weinberg et al. 2013). In contrast, we found that swsn-2.1 and swsn-2.2 are redundantly required for viability and they both function in parallel to ehn-3 in the somatic gonad. The overlapping functions of swsn-2.1 and swsn-2.2 in embryogenesis and gonadogenesis suggest that their divergence is evolutionarily recent. Consistent with this idea, the Drosophila genome contains a single Bap60 gene that is essential for viability (Moller et al. 2005). Because the repertoire of invertebrate accessory subunits is more limited than that of vertebrates, the utilization of BAF and PBAF subunits may play a more important role in the functional diversity of invertebrate SWI/SNF complexes.

Mammals have two homologs of SWSN-9, called BRD7 and BRD9. These proteins are found in different SWI/SNF complexes: BRD7 was purified as part of PBAF, whereas BRD9 was identified in BAF (Middeljans et al. 2012). Our phylogenetic analysis indicates that mammalian BRD7 and BRD9 are paralogs that resulted from a gene duplication event in the vertebrate lineage (Figure S3). We found that swsn-9 interacted strongly with ehn-3, including dominant enhancement of the ehn-3 phenotype. This is similar to PBAF genes and unlike the BAF gene let-526, suggesting that SWSN-9 is a PBAF subunit. We considered SWSN-9 as a potential BAF or PBAF subunit based on the mammalian biochemistry. However, our data are also consistent with the idea that SWSN-9 is a common accessory subunit and therefore is present in both BAF and PBAF complexes. In this scenario, BRD7 and BRD9 would have acquired complex specificity after the duplication of the Brd7/9 gene in vertebrates. Although we cannot distinguish between these possibilities, we favor the idea that SWSN-9 is a component of PBAF based on the striking similarity between the swsn-9 and pbrm-1 mutant phenotypes. An examination of other invertebrate Brd7/9 genes will shed light on the evolutionarily ancient role of this accessory subunit.

HND-1 and PBAF subunits are important for SGP fate determination

We originally proposed that hnd-1 was required for SGP survival, based on the following observations: hnd-1 mutants generated two SGPs in embryos; these SGPs were sometimes absent by the L1 larval stage; and cell corpses were present and correlated with missing SGPs (Mathies et al. 2003). Here, we show that hnd-1 mutants have SGPs that simultaneously express reporters typical of SGPs and their sisters, the hmcs. Based on this new evidence, we propose that hnd-1 SGPs fail to determine or maintain their fate and, as a result, they sometimes adopt a mixed SGP/hmc fate. This, in turn, could explain the higher incidence of missing Z1 cells (the sister of Z1 dies by programmed cell death) and the higher percentage of missing anterior gonadal arms (Z1 forms the anterior gonadal arm). Furthermore, we found that PBAF mutants share this phenotype with hnd-1 mutants, implicating SWI/SNF chromatin regulation in the molecular mechanisms that distinguish SGPs from their differentiated sisters.

The relationship between the SWI/SNF complex and HND-1 is complex. We found evidence that PBAF genes and hnd-1 are both required for SGP cell fate determination and we observed synergistic interactions between pbrm-1 and hnd-1 mutants. These observations are consistent with the idea hnd-1 and PBAF genes are partially redundant for the regulation of SGP cell fate determination genes. A variety of functional interactions between HND-1 and PBAF are possible. For example, PBAF may facilitate HND-1 binding to its target genes or, reciprocally, HND-1 may recruit PBAF to genomic regions that are important for SGP fate determination. Shibata et al. (2012) reported that pbrm-1 mutants have reduced hnd-1::GFP expression in SGPs. This might reflect a loss of SGP cell fate in pbrm-1 mutants, because hnd-1::GFP is an early marker for the SGP fate. Alternatively, hnd-1 and pbrm-1 may have different interactions in different cell types. hnd-1 is expressed dynamically in mesodermal lineages and later in SGPs (Mathies et al. 2003), and pbrm-1 is expressed broadly and perhaps ubiquitously (Shibata et al. 2012), providing ample opportunity for these genes to interact at multiple times in development. The identification of specific targets of HND-1 and PBRM-1 will allow us to explore these regulatory relationships at molecular and cellular levels.

Relationship between SWI/SNF and ehn-3

We initially investigated the SWI/SNF complex as a potential partner for EHN-3. The C. elegans HIL gene family includes ehn-3, which is expressed specifically in SGPs and is important for the development of several differentiated tissues of the somatic gonad (Large and Mathies 2010). Mammalian Ikaros interacts physically with SWI/SNF (Kim et al. 1999; O’Neill et al. 2000) and is likely to control immune system development by affecting the chromatin state in hematopoietic progenitor cells (Ng et al. 2007). Similarly, we hypothesized that EHN-3 might establish a permissive chromatin state in SGPs via direct interactions with chromatin remodeling complexes such as SWI/SNF. However, our results clearly indicate that PBAF subunits act in parallel to ehn-3. It remains possible that the SWI/SNF complex interacts physically with EHN-3 and that this interaction was masked by the function of SWI/SNF with hnd-1. In support of this idea, we note that ehn-3 and the BAF gene, let-526, are both required for the proper development of DTCs, and let-526 did not dominantly enhance the ehn-3 phenotype. Therefore, EHN-3 may act with BAF to promote DTC development. There are likely many multifaceted genetic and physical interactions between chromatin remodelers and cell-type–specific transcription factors. Genetic approaches will help to identify potential interaction partners, but biochemical approaches will ultimately be necessary to validate these interactions.

Distinct roles for BAF and PBAF subunits during cell lineage progression

The BAF and PBAF complexes are biochemically defined by the presence of unique “signature” subunits (Kwon and Wagner 2007; Mohrmann et al. 2004). Despite sharing a common enzymatic core and several accessory subunits, BAF and PBAF subunits have distinct activities in Drosophila development and mammalian gene regulation (Carrera et al. 2008; Kaeser et al. 2008; Mohrmann et al. 2004; Moshkin et al. 2007; Yan et al. 2005). We used tissue-specific RNAi to examine the function of C. elegans genes encoding core (swsn-4), BAF (let-526), and PBAF (pbrm-1) subunits. We found that pbrm-1 is important for SGP development, let-526 is important for DTC development, and swsn-4 is important for both SGP and DTC development. Our results are in agreement with a recent study characterizing let-526 and pbrm-1 mutants (Shibata et al. 2012), and they further implicate SWSN-4 as the catalytic subunit of SWI/SNF complexes in the somatic gonad. Together, these results provide strong support for the idea that distinct BAF and PBAF complexes control different processes during gonadogenesis. Drosophila BAP and PBAP complexes bind to different chromosomal sites and regulate distinct sets of target genes (Mohrmann et al. 2004; Moshkin et al. 2007). Similarly, we predict that C. elegans BAF and PBAF regulate distinct sets of target genes to control different processes in somatic gonadal development.

Recent results suggest a critical role for SWI/SNF complexes in the progression of multipotent progenitors to differentiated neurons in the mammalian nervous system. Distinct complexes are present in neural stem/progenitor cells (npBAF) and postmitotic neurons (nBAF) and result from the utilization of different paralogs of BAF45 and BAF57 (Lessard et al. 2007; Wu et al. 2007). The sequential utilization of SWI/SNF complexes may also be important in C. elegans hypodermal development, for which it has been suggested that the let-7 microRNA promotes a switch between BAF and PBAF complexes concomitant with differentiation in the hypodermis (Hayes et al. 2011). Here, we provide evidence that PBAF subunits are required in multipotent progenitors (SGPs), whereas BAF subunits are required in a differentiated cell type of the somatic gonad (DTCs). This suggests distinct SWI/SNF chromatin remodelers are utilized over the course of cell lineage progression and underscores the importance of dynamic gene expression changes accompanying the transition from multipotency to differentiation. With the fully defined cell lineage in C. elegans, one day it should be possible to map these gene expression changes onto the developmental program with single cell precision.