Regulation of transcription factor activity during cellular aging

被引:32
作者
Wheaton, K
Atadja, P
Riabowol, K
机构
[1] UNIV CALGARY,HLTH SCI CTR,DEPT MED BIOCHEM,CALGARY,AB T2N 4N1,CANADA
[2] UNIV CALGARY,HLTH SCI CTR,SO ALBERTA CANC RES CTR,CALGARY,AB T2N 4N1,CANADA
来源
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE | 1996年 / 74卷 / 04期
关键词
cellular aging; transcription; Fos; SRF; phosphorylation;
D O I
10.1139/o96-056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several lines of evidence suggest that the limited replication potential of normal human cells is due to the presence of an intrinsic genetic programme. This ''senescence programme'' is believed to reduce the incidence of cancer by limiting the growth of most of the transformed cells arising in vivo, although some cells do escape senescence becoming both immortalized and transformed. Here we review the literature that describes the senescence process in terms of gene expression and the regulation of gene expression by a variety of mechanisms affecting transcription factor activity. We focus on regulation of the c-fos gene through posttranslational modification of the serum response factor (SRF) as an example of altered gene expression during cellular aging.
引用
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页码:523 / 534
页数:12
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