Caenorhabditis elegans Reproductive Aging: Regulation and Underlying Mechanisms

被引:36
|
作者
Luo, Shijing [1 ]
Murphy, Coleen T. [1 ]
机构
[1] Princeton Univ, Lewis Sigler Inst Integrat Genom, Dept Mol Biol, Princeton, NJ 08544 USA
关键词
reproduction; aging; germ line; oocyte; C; elegans; GENOME-WIDE ASSOCIATION; OOCYTE MEIOTIC MATURATION; BETA PATHWAY COMPONENTS; PROGRAMMED CELL-DEATH; GERMLINE STEM-CELLS; INSULIN-LIKE GENE; AGE-1; PI3; KINASE; C-ELEGANS; LIFE-SPAN; TGF-BETA;
D O I
10.1002/dvg.20694
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Female reproductive decline is one of the first aging phenotypes in humans, manifested in increasing rates of infertility, miscarriage, and birth defects in children of mothers over 35. Recently, Caenorhabditis elegans (C. elegans) has been developed as a model to study reproductive aging, and several studies have advanced our knowledge of reproductive aging regulation in this organism. In this review, we describe our current understanding of reproductive cessation in C. elegans, including the relationship between oocyte quality, ovulation rate, progeny number, and reproductive span. We then discuss possible mechanisms of oocyte quality control, and provide an overview of the signaling pathways currently identified to be involved in reproductive span regulation in C. elegans. Finally, we extend the relevance of C. elegans reproductive aging studies to the issue of human female reproductive decline, and we discuss ideas concerning the relationship between reproductive aging and somatic longevity. genesis 49:53-65,2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:53 / 65
页数:13
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