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Makorin直系同源物LEP-2调节LIN-28的稳定性,以促进秀丽隐杆线虫从幼虫到成虫的转变。

Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans.

作者信息

Herrera R Antonio, Kiontke Karin, Fitch David H A

机构信息

Department of Biology, New York University, New York, NY 10003, USA.

Department of Biology, New York University, New York, NY 10003, USA Faculty of Arts and Sciences, New York University-Shanghai, Shanghai 200122, China

出版信息

Development. 2016 Mar 1;143(5):799-809. doi: 10.1242/dev.132738. Epub 2016 Jan 25.

Abstract

The heterochronic genes lin-28, let-7 and lin-41 regulate fundamental developmental transitions in animals, such as stemness versus differentiation and juvenile versus adult states. We identify a new heterochronic gene, lep-2, in Caenorhabditis elegans. Mutations in lep-2 cause a delay in the juvenile-to-adult transition, with adult males retaining pointed, juvenile tail tips, and displaying defective sexual behaviors. In both sexes, lep-2 mutants fail to cease molting or produce an adult cuticle. We find that LEP-2 post-translationally regulates LIN-28 by promoting LIN-28 protein degradation. lep-2 encodes the sole C. elegans ortholog of the Makorin (Mkrn) family of proteins. Like lin-28 and other heterochronic pathway members, vertebrate Mkrns are involved in developmental switches, including the timing of pubertal onset in humans. Based on shared roles, conservation and the interaction between lep-2 and lin-28 shown here, we propose that Mkrns, together with other heterochronic genes, constitute an evolutionarily ancient conserved module regulating switches in development.

摘要

异时性基因lin-28、let-7和lin-41调控动物体内的基本发育转变,如干性与分化以及幼虫与成虫状态之间的转变。我们在秀丽隐杆线虫中鉴定出一个新的异时性基因lep-2。lep-2突变导致幼虫到成虫的转变延迟,成年雄虫保留着尖锐的幼虫尾尖,并表现出有缺陷的性行为。在雌雄两性中,lep-2突变体都无法停止蜕皮或形成成虫表皮。我们发现LEP-2通过促进LIN-28蛋白降解对其进行翻译后调控。lep-2编码线虫中唯一的Makorin(Mkrn)家族蛋白直系同源物。与lin-28和其他异时性通路成员一样,脊椎动物的Mkrn参与发育转换,包括人类青春期开始的时间。基于此处所示的lep-2和lin-28的共同作用、保守性及相互作用,我们提出Mkrn与其他异时性基因共同构成了一个在进化上古老的保守模块,调控发育转换。

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