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DNA损伤诱导的程序性细胞死亡:在生殖细胞发育中的潜在作用。

DNA damage-induced programmed cell death: potential roles in germ cell development.

作者信息

Yamada Yukiko, Coffman Clark R

机构信息

Department of Genetics, Development and Cell Biology, Iowa State University, 3238 Molecular Biology Building, Ames, IA 50011-3260, USA.

出版信息

Ann N Y Acad Sci. 2005 May;1049:9-16. doi: 10.1196/annals.1334.002.

Abstract

The detection of DNA damage is necessary to protect against proliferation of potentially harmful cells and often results in cell cycle arrest and programmed cell death. Key components of DNA damage signaling networks include ATM, CHK2, p53, and Bax. Mutations in these damage signaling systems are linked to tumorigenesis and developmental abnormalities. Expression of some of these genes in primordial germ cells (PGCs) argues that PGCs may utilize DNA damage-induced signaling mechanisms to select against germ cells that are genetically defective, thus maintaining the integrity of the germline. This paper summarizes the roles of these DNA damage signaling molecules and addresses their potential involvement in germ cell development.

摘要

检测DNA损伤对于防止潜在有害细胞的增殖是必要的,并且常常导致细胞周期停滞和程序性细胞死亡。DNA损伤信号网络的关键组成部分包括ATM、CHK2、p53和Bax。这些损伤信号系统中的突变与肿瘤发生和发育异常有关。这些基因中的一些在原始生殖细胞(PGC)中的表达表明,PGC可能利用DNA损伤诱导的信号机制来筛选出有基因缺陷的生殖细胞,从而维持种系的完整性。本文总结了这些DNA损伤信号分子的作用,并探讨了它们在生殖细胞发育中的潜在参与情况。

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