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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共 87 条
[51]   PANTHER version 14: more genomes, a new PANTHER GO-slim and improvements in enrichment analysis tools [J].
Mi, Huaiyu ;
Muruganujan, Anushya ;
Ebert, Dustin ;
Huang, Xiaosong ;
Thomas, Paul D. .
NUCLEIC ACIDS RESEARCH, 2019, 47 (D1) :D419-D426
[52]   PANTHER in 2013: modeling the evolution of gene function, and other gene attributes, in the context of phylogenetic trees [J].
Mi, Huaiyu ;
Muruganujan, Anushya ;
Thomas, Paul D. .
NUCLEIC ACIDS RESEARCH, 2013, 41 (D1) :D377-D386
[53]   CHIP deficiency decreases longevity, with accelerated aging phenotypes accompanied by altered protein quality control [J].
Min, Jin-Na ;
Whaley, Ryan A. ;
Sharpless, Norman E. ;
Lockyer, Pamela ;
Portbury, Andrea L. ;
Patterson, Cam .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (12) :4018-4025
[54]   CELLS IN STRESS - TRANSCRIPTIONAL ACTIVATION OF HEAT-SHOCK GENES [J].
MORIMOTO, RI .
SCIENCE, 1993, 259 (5100) :1409-1410
[55]   Regulation of longevity in Caenorhabditis elegans by heat shock factor and molecular chaperones [J].
Morley, JF ;
Morimoto, RI .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (02) :657-664
[56]   Overexpression of the small mitochondrial Hsp22 extends Drosophila life span and increases resistance to oxidative stress [J].
Morrow, G ;
Samson, M ;
Michaud, S ;
Tanguay, RM .
FASEB JOURNAL, 2004, 18 (01) :598-+
[57]   Heat shock transcription factor 1 as a therapeutic target in neurodegenerative diseases [J].
Neef, Daniel W. ;
Jaeger, Alex M. ;
Thiele, Dennis J. .
NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (12) :930-944
[58]   JNK regulates lifespan in Caenorhabditis elegans by modulating nuclear translocation of forkhead transcription factor/DAF-16 [J].
Oh, SW ;
Mukhopadhyay, A ;
Svrzikapa, N ;
Jiang, F ;
Davis, RJ ;
Tissenbaum, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (12) :4494-4499
[59]   Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 [J].
Ophoff, RA ;
Terwindt, GM ;
Vergouwe, MN ;
vanEijk, R ;
Oefner, PJ ;
Hoffman, SMG ;
Lamerdin, JE ;
Mohrenweiser, HW ;
Bulman, DE ;
Ferrari, M ;
Haan, J ;
Lindhout, D ;
vanOmmen, GJB ;
Hofker, MH ;
Ferrari, MD ;
Frants, RR .
CELL, 1996, 87 (03) :543-552
[60]   TRAIL regulates collagen production through HSF1-dependent Hsp47 expression in activated hepatic stellate cells [J].
Park, Soo-Jung ;
Sohn, Hee-Young ;
Park, Sang Ick .
CELLULAR SIGNALLING, 2013, 25 (07) :1635-1643