4.7 Article

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

期刊

出版社

MDPI
DOI: 10.3390/ijms20225815

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

资金

  1. MEDinPROT Protein Science Research Synergy Program (by the Hungarian Academy of Sciences
  2. HAS)
  3. VEKOP grant [VEKOP-2.3.2-16-2017-00014]
  4. National Research, Development and Innovation Office [NKFIH-1157-8/2019-DT]
  5. National Research, Development and Innovation. Fund of Hungary [2018-1.2.1-NKP-2018-00005, 2018-1.2.1-NKP]
  6. MTA-ELTE Genetics Research Group [01062]
  7. BBSRC [BBS/E/T/000PR9819] Funding Source: UKRI

向作者/读者索取更多资源

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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