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首页> 外文期刊>Developmental biology >Novel gain-of-function alleles demonstrate a role for the heterochronic gene lin-41 in C. elegans male tail tip morphogenesis.
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Novel gain-of-function alleles demonstrate a role for the heterochronic gene lin-41 in C. elegans male tail tip morphogenesis.

机译:新的功能获得等位基因表明线粒体雄性尾尖形态发生中的异时基因lin-41的作用。

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摘要

To gain an understanding of the genes and mechanisms that govern morphogenesis and its evolution, we have analyzed mutations that disrupt this process in a simple model structure, the male tail tip of the rhabditid nematode C. elegans. During the evolution of rhabditid male tails, there have been several independent changes from tails with rounded tips ("peloderan", as in C. elegans) to those with pointed tips ("leptoderan"). Mutations which produce leptoderan (Lep) tails in C. elegans thus identify candidate genes and pathways in which evolutionary changes could have produced leptoderan tails from peloderan ancestors. Here we report that two novel, gain-of-function (gf) alleles of lin-41 have lesions predicted to affect the N-terminus of the RBCC-domain LIN-41 protein. Both gf alleles cause the tail tip of adult males to retain the pointed shape of the juvenile tails, producing a Lep phenotype that looks like the tails of leptoderan species. Consistent with its role in the heterochronic pathway, we find that lin-41 governs the timing and extent of male tail tip morphogenesis in a dose-dependent manner. Specifically, the Lep phenotype results from a heterochronic delay in the retraction and fusion of the tail tip cells during L4 morphogenesis, such that retraction is not completed before the adult molt. Conversely, we find that tail tip morphogenesis and cell fusions begin precociously at the L3 stage in the reduced-function lin-41 mutant, ma104, resulting in over-retracted male tails in the adult. Because modulated anti-LIN-41 RNAi knockdowns in the gf mutants restore wild-type phenotype, we suggest that the leptoderan phenotype of the gf alleles is due to a higher activity of otherwise normal LIN-41. Additionally, the gf allele is suppressed by the wild-type allele, suggesting that LIN-41 normally regulates itself, possibly by autoubiquitination. We speculate that small changes affecting LIN-41 could have been significant for male tail evolution.
机译:为了了解控制形态发生及其进化的基因和机制,我们已经分析了在简单的模型结构(大戟线虫秀丽线虫的雄性尾尖)中破坏该过程的突变。在大黄蜂雄性尾巴的进化过程中,有一些独立的变化,从具有圆形尖端的尾巴(如线虫中的“ peloderan”)到具有尖端的尾巴(“ leptoderan”)。因此,在秀丽隐杆线虫中产生leptoderan(Lep)尾巴的突变可识别候选基因和途径,在这些基因和途径中,进化变化可能已从peloderan祖先产生了leptoderan尾巴。在这里,我们报道了lin-41的两个新的功能获得(gf)等位基因具有预计会影响RBCC域LIN-41蛋白N端的损伤。这两个gf等位基因均导致成年男性的尾尖保持少年尾巴的尖头形状,产生看起来像瘦小体物种尾巴的Lep表型。与其在异时途径中的作用一致,我们发现lin-41以剂量依赖的方式控制雄性尾尖形态发生的时间和程度。具体而言,Lep表型是由于在L4形态发生过程中尾尖细胞回缩和融合的异时延迟导致的,因此在成年蜕皮之前回缩未完成。相反,我们发现尾巴形态发生和细胞融合在功能降低的lin-41突变体ma104中的L3阶段早熟开始,导致成年雄性尾巴过度缩回。因为gf突变体中的经过调节的抗LIN-41 RNAi敲低恢复了野生型表型,所以我们建议gf等位基因的leptoderan表型归因于正常LIN-41的更高活性。此外,gf等位基因被野生型等位基因抑制,这表明LIN-41可能通过自身泛素化正常调节自身。我们推测影响LIN-41的微小变化对于雄性尾巴进化可能具有重要意义。

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