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Hox 和新鉴定的 E2F 共同抑制秀丽隐杆线虫的细胞死亡。

Hox and a newly identified E2F co-repress cell death in Caenorhabditis elegans.

机构信息

Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, Texas 75235-9148, USA.

出版信息

Genetics. 2011 Aug;188(4):897-905. doi: 10.1534/genetics.111.128421. Epub 2011 May 19.

Abstract

The development of an organism depends on individual cells receiving and executing their specific fates, although how this process is regulated remains largely unknown. Here, we identify a mechanism by which a specific cell fate, apoptosis, is determined through the cooperative efforts of Hox and E2F proteins. E2F transcription factors are critical, conserved regulators of the cell cycle and apoptosis. However, little is known about the two most recently discovered mammalian E2Fs-E2F7 and E2F8. In the nematode Caenorhabditis elegans, we identify a novel E2F7/8 homolog, EFL-3, and show that EFL-3 functions cooperatively with LIN-39, providing the first example in which these two major developmental pathways-E2F and Hox-are able to directly regulate the same target gene. Our studies demonstrate that LIN-39 and EFL-3 function in a cell type-specific context to regulate transcription of the egl-1 BH3-only cell death gene and to determine cell fate during development.

摘要

生物体的发育依赖于个体细胞接收并执行其特定命运的能力,尽管这一过程如何被调控在很大程度上仍是未知的。在这里,我们发现了一种机制,通过该机制,特定的细胞命运——凋亡,是通过 Hox 和 E2F 蛋白的协同作用来决定的。E2F 转录因子是细胞周期和凋亡的关键、保守的调控因子。然而,对于最近发现的两种哺乳动物 E2Fs-E2F7 和 E2F8,人们知之甚少。在线虫秀丽隐杆线虫中,我们鉴定出一种新型的 E2F7/8 同源物 EFL-3,并表明 EFL-3 与 LIN-39 协同作用,这提供了第一个例证,即这两个主要的发育途径——E2F 和 Hox——能够直接调控同一靶基因。我们的研究表明,LIN-39 和 EFL-3 在细胞类型特异性的背景下发挥作用,调节 egl-1 BH3 仅细胞死亡基因的转录,并在发育过程中决定细胞命运。

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