Regulation of HSF1 Function in the Heat Stress Response: Implications in Aging and Disease

被引:575
作者
Anckar, Julius [1 ,2 ]
Sistonen, Lea [1 ,2 ]
机构
[1] Abo Akad Univ, Dept Biosci, Biocity 20520, Turku, Finland
[2] Univ Turku, Ctr Biotechnol, Biocity 20520, Turku, Finland
来源
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80 | 2011年 / 80卷
关键词
heat shock factor; longevity; posttranslational modification; proteostasis; transcription; SHOCK TRANSCRIPTION FACTOR; RNA-POLYMERASE-II; DNA-BINDING DOMAIN; GENOME-WIDE ANALYSIS; AGE-RELATED DISEASE; P-TEFB KINASE; IN-VIVO; CAENORHABDITIS-ELEGANS; LIFE-SPAN; MOLECULAR CHAPERONES;
D O I
10.1146/annurev-biochem-060809-095203
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
To dampen proteotoxic stresses and maintain protein homeostasis, organisms possess a stress-responsive molecular machinery that detects and neutralizes protein damage. A prominent feature of stressed cells is the increased synthesis of heat shock proteins (Hsps) that aid in the refolding of misfolded peptides and restrain protein aggregation. Transcriptional activation of the heat shock response is orchestrated by heat shock factor 1 (HSF1), which rapidly translocates to hsp genes and induces their expression. Although the role of HSF1 in protecting cells and organisms against severe stress insults is well established, many aspects of how HSF1 senses qualitatively and quantitatively different forms of stresses have remained poorly understood. Moreover, recent discoveries that HSF1 controls life span have prompted new ways of thinking about an old transcription factor. Here, we review the established role of HSF1 in counteracting cell stress and prospect the role of HSF1 as a regulator of disease states and aging.
引用
收藏
页码:1089 / 1115
页数:27
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