Drosophila melanogaster p53 has developmental stage-specific and sex-specific effects on adult life span indicative of sexual antagonistic pleiotropy

被引:56
|
作者
Waskar, Morris [1 ]
Landis, Gary N. [1 ]
Shen, Jie [1 ]
Curtis, Christina [1 ,2 ]
Tozer, Kevin [1 ]
Abdueva, Diana [1 ]
Skvortsov, Dmitriy [1 ]
Tavare, Simon [1 ,2 ]
Tower, John [1 ]
机构
[1] Univ So Calif, Dept Biol Sci, Mol & Computat Biol Program, Los Angeles, CA 90089 USA
[2] Univ Cambridge, Dept Oncol, Canc Res UK, Li Ka Shing Ctr,Cambridge Res Inst, Cambridge CB2 0RE, England
来源
AGING-US | 2009年 / 1卷 / 11期
关键词
aging; sexual conflict; Geneswitch; maternal effects; tumor suppressor; TUMOR-SUPPRESSOR P53; TRANSGENE EXPRESSION; GENE-EXPRESSION; DAMAGE RESPONSE; DNA-DAMAGE; STEM-CELLS; CANCER; PROTECTS; MICE; EVOLUTIONARY;
D O I
10.18632/aging.100099
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Truncated and mutant forms of p53 affect life span in Drosophila, nematodes and mice, however the role of wildtype p53 in aging remains unclear. Here conditional over-expression of both wild-type and mutant p53 transgenes indicated that, in adult flies, p53 limits life span in females but favors life span in males. In contrast, during larval development, moderate over-expression of p53 produced both male and female adults with increased life span. Mutations of the endogenous p53 gene also had sex-specific effects on life span under control and stress conditions: null mutation of p53 increased life span in females, and had smaller, more variable effects in males. These developmental stage-specific and sex-specific effects of p53 on adult life span are consistent with a sexual antagonistic pleiotropy model.
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页码:903 / 936
页数:34
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