HSF1Base: A Comprehensive Database of HSF1 (Heat Shock Factor 1) Target Genes

被引:63
作者
Kovacs, Daniel [1 ]
Sigmond, Timea [1 ]
Hotzi, Bernadette [1 ]
Bohar, Balazs [1 ,2 ,3 ]
Fazekas, David [1 ,2 ,3 ]
Deak, Veronika [4 ]
Vellai, Tibor [1 ,5 ]
Barna, Janos [1 ,5 ]
机构
[1] Eotvos Lorand Univ, Dept Genet, Inst Biol, Pazmany Peter Stny 1-C, H-1117 Budapest, Hungary
[2] Earlham Inst, Norwich NR4 7UZ, Norfolk, England
[3] Quadram Inst, Norwich NR4 7UA, Norfolk, England
[4] Univ Technol, Dept Appl Biotechnol & Food Sci, Lab Biochem & Mol Biol, H-1111 Budapest, Hungary
[5] Eotvos Lorand Univ, MTA ELTE Genet Res Grp, H-1117 Budapest, Hungary
基金
英国生物技术与生命科学研究理事会;
关键词
ageing; autophagy; cell adhesion; cell cycle; circadian rhythm; chromatin remodeling; heat shock factor 1; heat shock proteins; heat shock response; ribosome biogenesis; TRANSCRIPTION FACTOR-1; LIFE-SPAN; CAENORHABDITIS-ELEGANS; STRESS; EXPRESSION; MECHANISMS; CHROMATIN; AUTOPHAGY; JUN; IDENTIFICATION;
D O I
10.3390/ijms20225815
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
HSF1 (heat shock factor 1) is an evolutionarily conserved master transcriptional regulator of the heat shock response (HSR) in eukaryotic cells. In response to high temperatures, HSF1 upregulates genes encoding molecular chaperones, also called heat shock proteins, which assist the refolding or degradation of damaged intracellular proteins. Accumulating evidence reveals however that HSF1 participates in several other physiological and pathological processes such as differentiation, immune response, and multidrug resistance, as well as in ageing, neurodegenerative demise, and cancer. To address how HSF1 controls these processes one should systematically analyze its target genes. Here we present a novel database called HSF1Base (hsf1base.org) that contains a nearly comprehensive list of HSF1 target genes identified so far. The list was obtained by manually curating publications on individual HSF1 targets and analyzing relevant high throughput transcriptomic and chromatin immunoprecipitation data derived from the literature and the Yeastract database. To support the biological relevance of HSF1 targets identified by high throughput methods, we performed an enrichment analysis of (potential) HSF1 targets across different tissues/cell types and organisms. We found that general HSF1 functions (targets are expressed in all tissues/cell types) are mostly related to cellular proteostasis. Furthermore, HSF1 targets that are conserved across various animal taxa operate mostly in cellular stress pathways (e.g., autophagy), chromatin remodeling, ribosome biogenesis, and ageing. Together, these data highlight diverse roles for HSF1, expanding far beyond the HSR.
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页数:24
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