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核受体基因 nhr-25 在秀丽隐杆线虫的异时性基因网络中发挥多种作用,以控制幼虫到成虫的过渡。

The nuclear receptor gene nhr-25 plays multiple roles in the Caenorhabditis elegans heterochronic gene network to control the larva-to-adult transition.

机构信息

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan.

出版信息

Dev Biol. 2010 Aug 15;344(2):1100-9. doi: 10.1016/j.ydbio.2010.05.508. Epub 2010 Jun 2.

Abstract

Developmental timing in the nematode Caenorhabditis elegans is controlled by heterochronic genes, mutations in which cause changes in the relative timing of developmental events. One of the heterochronic genes, let-7, encodes a microRNA that is highly evolutionarily conserved, suggesting that similar genetic pathways control developmental timing across phyla. Here we report that the nuclear receptor nhr-25, which belongs to the evolutionarily conserved fushi tarazu-factor 1/nuclear receptor NR5A subfamily, interacts with heterochronic genes that regulate the larva-to-adult transition in C. elegans. We identified nhr-25 as a regulator of apl-1, a homolog of the Alzheimer's amyloid precursor protein-like gene that is downstream of let-7 family microRNAs. NHR-25 controls not only apl-1 expression but also regulates developmental progression in the larva-to-adult transition. NHR-25 negatively regulates the expression of the adult-specific collagen gene col-19 in lateral epidermal seam cells. In contrast, NHR-25 positively regulates the larva-to-adult transition for other timed events in seam cells, such as cell fusion, cell division and alae formation. The genetic relationships between nhr-25 and other heterochronic genes are strikingly varied among several adult developmental events. We propose that nhr-25 has multiple roles in both promoting and inhibiting the C. elegans heterochronic gene pathway controlling adult differentiation programs.

摘要

线虫秀丽隐杆线虫的发育时间由异型基因控制,这些基因的突变会导致发育事件的相对时间发生变化。异型基因之一 let-7 编码一种高度进化保守的 microRNA,这表明类似的遗传途径控制着不同门的发育时间。在这里,我们报告说核受体 nhr-25 与调控秀丽隐杆线虫幼虫到成虫过渡的异型基因相互作用,nhr-25 属于进化保守的 fushi tarazu-factor 1/核受体 NR5A 亚家族。我们确定 nhr-25 是 apl-1 的调节剂,apl-1 是阿尔茨海默病淀粉样前体蛋白样基因的同源物,位于 let-7 家族 microRNA 的下游。NHR-25 不仅控制 apl-1 的表达,还调节幼虫到成虫过渡的发育进展。NHR-25 负调控侧表皮 seam 细胞中成年特异性胶原基因 col-19 的表达。相比之下,NHR-25 对 seam 细胞中其他定时事件(如细胞融合、细胞分裂和翅片形成)的幼虫到成虫过渡具有正调控作用。nhr-25 和其他异型基因之间的遗传关系在几个成年发育事件中差异显著。我们提出 nhr-25 在促进和抑制秀丽隐杆线虫异型基因途径控制成虫分化程序方面具有多种作用。

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