Molecular genetic study of reproductive system development in C. elegans and related nematode species

线虫及相关线虫物种生殖系统发育的分子遗传学研究

• 批准号: RGPIN-2020-06912
• 负责人: Gupta, Bhagwati
• 金额: $ 3.64万
• 依托单位: McMaster University
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2022
• 资助国家: 加拿大
• 起止时间: 2022-01-01 至 2023-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=745727
• 关键词: Molecular; genetic; study; reproductive; system

My NSERC-funded research program focuses on understanding genetic networks that control organ formation in eukaryotes by dissecting molecular mechanisms of similarities and differences in gene function in nematodes. To this end, we are conducting a comparative analysis of reproductive system development, specifically the hermaphrodite vulva, in the nematode (worm) Caenorhabditis elegans and its sister species C. briggsae. A large collection of   mutants were isolated earlier in our lab through forward genetic screens. The mutants belong to three distinct phenotypic classes: vulvaless (Vul), multivulva (Muv), and protruding vulva (Pvl). To date, 17 Vul, Muv and Pvl genes have been studied in some detail. Ten of these are cloned and function investigated in some detail (Seetharaman et al., Dev Biol 2010; Sharanya et al., G3 2012; Sharanya et al., Evol Chamberlin et al., manuscript under review). These genes function at different steps of the vulval induction process and participate in Wnt-beta-Catenin and EGFR-Ras signalling pathways. Interestingly, we have also uncovered evolutionary changes in some of the genes, leading us to propose that developmental mechanisms have diverged between the two nematode species. NSERC funding will enable us to further investigate the mechanism of evolutionary changes in gene function and pathways. Towards this, we will be focusing on the Muv genes that show differences in cell induction pattern compared to the C. elegans orthologs. In collaboration with Dr. Chamberlin's lab (Ohio State), we have molecularly characterized four of the Muv mutants that define a new phenotypic class termed 'inappropriate vulva proliferation (ivp).' The genes are Cbr-htz-1 (H2A.z), Cbr-spr-4 (REST/NRSF), Cbr-gon-14 (hAT transposon family), and Cbr-ivp-3 (Ribonuclease H-like superfamily). Although all four genes are conserved in C. elegans, there are major functional differences. While mutations in any of the C. elegans orthologs, except gon-14, cause normal vulva phenotype, C. briggsae mutants are nearly fully penetrant Muv. To understand the genetic pathway of ivp genes, RNA-seq experiment was carried out. The results revealed that C. briggsae Muv mutants exhibit misregulation of germline genes, leading us to propose that the Muv genes may act to promote differentiation of somatic cells. Future experiments will focus on understanding the mechanism of action of ivp genes in C. briggsae and their functional differences from C. elegans. To this end, we plan to characterize the interacting genes and downstream targets through a combination of forward and reverse genetic (such as CRISPR and RNAi) approaches. These experiments should reveal whether C. briggsae Muv genes define new pathways by altered regulation of known C. elegans orthologs or whether existing developmental pathways are used differently. Ultimately, the findings will uncover the conservation and divergence in developmental mechanisms in metazoans.

我的NSERC资助的研究计划的重点是通过解剖线虫基因功能的相似性和差异的分子机制，了解控制真核生物器官形成的遗传网络。为此，我们正在进行生殖系统发育的比较分析，特别是两性外阴，在线虫（蠕虫）秀丽隐杆线虫和它的姐妹物种C。布里格塞 的大集合 我们实验室早先通过正向遗传筛选分离出了突变体。突变体属于三种不同的表型类别：外阴无（Vul），多外阴（Muv），和突出外阴（Pvl）。迄今为止，已经对17个Vul、Muv和Pvl基因进行了详细研究。克隆了其中的10个，并对其功能进行了详细研究（Seetharaman等人，Dev Biol 2010; Sharanya等人，G3 2012; Sharanya等人，Evol Chamberlin等人，正在审查的手稿）。这些基因在外阴诱导过程的不同步骤中发挥作用，并参与Wnt-β-连环蛋白和EGFR-Ras信号通路。有趣的是，我们还发现了一些基因的进化变化，这使我们提出两种线虫物种之间的发育机制有所不同。NSERC的资助将使我们能够进一步研究基因功能和途径的进化变化机制。为此，我们将集中在Muv基因，显示细胞诱导模式的差异相比，C。elegans直向同源物。 与Chamberlin博士的实验室（俄亥俄州）合作，我们对四种Muv突变体进行了分子特征分析，这些突变体定义了一种新的表型，称为“不适当外阴增殖（ivp）”。这些基因是Cbr-htz-1（H2A.z）、Cbr-spr-4（REST/NRSF）、Cbr-gon-14（hAT转座子家族）和Cbr-ivp-3（核糖核酸酶H样超家族）。虽然这四个基因在C.在功能上有很大的差异。而C.除gon-14外，秀丽隐杆线虫的同源基因引起正常外阴表型，C. Briggsae突变体几乎完全渗透Muv。 为了了解ivp基因的遗传途径，进行了RNA-seq实验。结果表明，C. Briggsae Muv突变体表现出生殖系基因的失调，这使我们提出Muv基因可能起促进体细胞分化的作用。未来的实验将集中在理解ivp基因在C. briggsae的功能及其与C.优美的为此，我们计划通过正向和反向遗传（如CRISPR和RNAi）方法的组合来表征相互作用的基因和下游靶标。这些实验将揭示C. Briggsae Muv基因通过改变已知C. elegans直系同源物或现有的发育途径是否被不同地使用。最终，这些发现将揭示后生动物发育机制的保守性和差异性。