Coordinated Transcriptional Regulation of Hspa1a Gene by Multiple Transcription Factors: Crucial Roles for HSF-1, NF-Y, NF-κB, and CREB

Although the transcript level of inducible heat shock protein 70.3 (Hsp70.3, also known as Hspa1a) is altered in various disease states, its transcriptional regulation remains incompletely understood. Here, we systematically analyzed the Hspa1a promoter to identify major cis elements and transcripti...

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Veröffentlicht in:Journal of molecular biology 2014-01, Vol.426 (1), p.116-135
Hauptverfasser: Sasi, Binu K., Sonawane, Parshuram J., Gupta, Vinayak, Sahu, Bhavani S., Mahapatra, Nitish R.
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container_issue 1
container_start_page 116
container_title Journal of molecular biology
container_volume 426
creator Sasi, Binu K.
Sonawane, Parshuram J.
Gupta, Vinayak
Sahu, Bhavani S.
Mahapatra, Nitish R.
description Although the transcript level of inducible heat shock protein 70.3 (Hsp70.3, also known as Hspa1a) is altered in various disease states, its transcriptional regulation remains incompletely understood. Here, we systematically analyzed the Hspa1a promoter to identify major cis elements and transcription factors that may govern the constitutive/inducible gene expression. Computational analyses coupled with extensive in vitro (promoter–reporter activity and electrophoretic mobility shift assays) and in vivo (chromatin immunoprecipitation assays) revealed interaction of several transcription factors with Hspa1a promoter motifs: HSF-1 (heat shock factor 1) at −114/−97bp and −788/−777bp, NF-Y (nuclear transcription factor Y) at −73/−58bp, NF-κB (nuclear factor kappa B) at −133/−124bp, and CREB (cAMP response element binding protein) at −483/−476bp. Consistently, siRNA (small interfering RNA)-mediated down-regulation of each of these transcription factors caused substantial reduction of endogenous Hspa1a expression. Heat-shock-induced activation of Hspa1a was coordinately regulated by HSF-1 and NF-Y/NF-κB. The Hspa1a expression was augmented by TNF-α (tumor necrosis factor-alpha) and forskolin in NF-κB and CREB-dependent manners, respectively. NF-κB and CREB also activated Hspa1a transcription in cardiac myoblasts upon exposure to ischemia-like conditions. Taken together, this study discovered previously unknown roles for NF-κB and CREB to regulate Hspa1a expression and a coordinated action by several transcription factors for Hspa1a transactivation under heat-shock/ischemia-like conditions and thereby provided new insights into the mechanism of Hspa1a regulation. [Display omitted] •Expression of the heat shock protein Hspa1a is altered in various disease states.•Transcriptional regulation of Hspa1a gene was systematically analyzed in this study.•Interaction of several transcription factors with Hspa1a promoter was discovered.•CREB, NF-Y, and NF-kB synergistically regulate heat-shock-induced Hspa1a expression.•CREB and NF-κB emerged as novel regulators of Hspa1a gene expression.
doi_str_mv 10.1016/j.jmb.2013.09.008
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Here, we systematically analyzed the Hspa1a promoter to identify major cis elements and transcription factors that may govern the constitutive/inducible gene expression. Computational analyses coupled with extensive in vitro (promoter–reporter activity and electrophoretic mobility shift assays) and in vivo (chromatin immunoprecipitation assays) revealed interaction of several transcription factors with Hspa1a promoter motifs: HSF-1 (heat shock factor 1) at −114/−97bp and −788/−777bp, NF-Y (nuclear transcription factor Y) at −73/−58bp, NF-κB (nuclear factor kappa B) at −133/−124bp, and CREB (cAMP response element binding protein) at −483/−476bp. Consistently, siRNA (small interfering RNA)-mediated down-regulation of each of these transcription factors caused substantial reduction of endogenous Hspa1a expression. Heat-shock-induced activation of Hspa1a was coordinately regulated by HSF-1 and NF-Y/NF-κB. The Hspa1a expression was augmented by TNF-α (tumor necrosis factor-alpha) and forskolin in NF-κB and CREB-dependent manners, respectively. NF-κB and CREB also activated Hspa1a transcription in cardiac myoblasts upon exposure to ischemia-like conditions. Taken together, this study discovered previously unknown roles for NF-κB and CREB to regulate Hspa1a expression and a coordinated action by several transcription factors for Hspa1a transactivation under heat-shock/ischemia-like conditions and thereby provided new insights into the mechanism of Hspa1a regulation. 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The Hspa1a expression was augmented by TNF-α (tumor necrosis factor-alpha) and forskolin in NF-κB and CREB-dependent manners, respectively. NF-κB and CREB also activated Hspa1a transcription in cardiac myoblasts upon exposure to ischemia-like conditions. Taken together, this study discovered previously unknown roles for NF-κB and CREB to regulate Hspa1a expression and a coordinated action by several transcription factors for Hspa1a transactivation under heat-shock/ischemia-like conditions and thereby provided new insights into the mechanism of Hspa1a regulation. 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The Hspa1a expression was augmented by TNF-α (tumor necrosis factor-alpha) and forskolin in NF-κB and CREB-dependent manners, respectively. NF-κB and CREB also activated Hspa1a transcription in cardiac myoblasts upon exposure to ischemia-like conditions. Taken together, this study discovered previously unknown roles for NF-κB and CREB to regulate Hspa1a expression and a coordinated action by several transcription factors for Hspa1a transactivation under heat-shock/ischemia-like conditions and thereby provided new insights into the mechanism of Hspa1a regulation. 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subjects Artificial Gene Fusion
CCAAT-Binding Factor - metabolism
Chromatin Immunoprecipitation
Computational Biology
Cyclic AMP Response Element-Binding Protein - metabolism
DNA-Binding Proteins - metabolism
Electrophoretic Mobility Shift Assay
gene expression
Gene Expression Regulation
Genes, Reporter
heat shock protein
Heat Shock Transcription Factors
HSP70 Heat-Shock Proteins - biosynthesis
NF-kappa B - metabolism
regulatory motifs
transcription factors
Transcription Factors - metabolism
Transcription, Genetic
title Coordinated Transcriptional Regulation of Hspa1a Gene by Multiple Transcription Factors: Crucial Roles for HSF-1, NF-Y, NF-κB, and CREB
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