Regulation of HuR by DNA Damage Response Kinases

As many DNA-damaging conditions repress transcription, posttranscriptional processes critically influence gene expression during the genotoxic stress response. The RNA-binding protein HuR robustly influences gene expression following DNA damage. HuR function is controlled in two principal ways: (1)...

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Main Authors: Hyeon Ho Kim, Kotb Abdelmohsen, Myriam Gorospe
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Journal of Nucleic Acids
Online Access:http://dx.doi.org/10.4061/2010/981487
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author Hyeon Ho Kim
Kotb Abdelmohsen
Myriam Gorospe
author_facet Hyeon Ho Kim
Kotb Abdelmohsen
Myriam Gorospe
author_sort Hyeon Ho Kim
collection DOAJ
description As many DNA-damaging conditions repress transcription, posttranscriptional processes critically influence gene expression during the genotoxic stress response. The RNA-binding protein HuR robustly influences gene expression following DNA damage. HuR function is controlled in two principal ways: (1) by mobilizing HuR from the nucleus to the cytoplasm, where it modulates the stability and translation of target mRNAs and (2) by altering its association with target mRNAs. Here, we review evidence that two main effectors of ataxia-telangiectasia-mutated/ATM- and Rad3-related (ATM/ATR), the checkpoint kinases Chk1 and Chk2, jointly influence HuR function. Chk1 affects HuR localization by phosphorylating (hence inactivating) Cdk1, a kinase that phosphorylates HuR and thereby blocks HuR's cytoplasmic export. Chk2 modulates HuR binding to target mRNAs by phosphorylating HuR's RNA-recognition motifs (RRM1 and RRM2). We discuss how HuR phosphorylation by kinases including Chk1/Cdk1 and Chk2 impacts upon gene expression patterns, cell proliferation, and survival following genotoxic injury.
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spelling doaj-art-44c0dce8a6864aa8b2a9f8f16cebd6d32025-08-20T02:37:46ZengWileyJournal of Nucleic Acids2090-021X2010-01-01201010.4061/2010/981487981487Regulation of HuR by DNA Damage Response KinasesHyeon Ho Kim0Kotb Abdelmohsen1Myriam Gorospe2Laboratory of Cellular and Molecular Biology, NIA-IRP, NIH, Baltimore, MD 21224, USALaboratory of Cellular and Molecular Biology, NIA-IRP, NIH, Baltimore, MD 21224, USALaboratory of Cellular and Molecular Biology, NIA-IRP, NIH, Baltimore, MD 21224, USAAs many DNA-damaging conditions repress transcription, posttranscriptional processes critically influence gene expression during the genotoxic stress response. The RNA-binding protein HuR robustly influences gene expression following DNA damage. HuR function is controlled in two principal ways: (1) by mobilizing HuR from the nucleus to the cytoplasm, where it modulates the stability and translation of target mRNAs and (2) by altering its association with target mRNAs. Here, we review evidence that two main effectors of ataxia-telangiectasia-mutated/ATM- and Rad3-related (ATM/ATR), the checkpoint kinases Chk1 and Chk2, jointly influence HuR function. Chk1 affects HuR localization by phosphorylating (hence inactivating) Cdk1, a kinase that phosphorylates HuR and thereby blocks HuR's cytoplasmic export. Chk2 modulates HuR binding to target mRNAs by phosphorylating HuR's RNA-recognition motifs (RRM1 and RRM2). We discuss how HuR phosphorylation by kinases including Chk1/Cdk1 and Chk2 impacts upon gene expression patterns, cell proliferation, and survival following genotoxic injury.http://dx.doi.org/10.4061/2010/981487
spellingShingle Hyeon Ho Kim
Kotb Abdelmohsen
Myriam Gorospe
Regulation of HuR by DNA Damage Response Kinases
Journal of Nucleic Acids
title Regulation of HuR by DNA Damage Response Kinases
title_full Regulation of HuR by DNA Damage Response Kinases
title_fullStr Regulation of HuR by DNA Damage Response Kinases
title_full_unstemmed Regulation of HuR by DNA Damage Response Kinases
title_short Regulation of HuR by DNA Damage Response Kinases
title_sort regulation of hur by dna damage response kinases
url http://dx.doi.org/10.4061/2010/981487
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AT kotbabdelmohsen regulationofhurbydnadamageresponsekinases
AT myriamgorospe regulationofhurbydnadamageresponsekinases