Medical Journals

Regulation of Gene Transcription by Mitogen-activated Protein Kinase Signaling Pathways.

Authors:
  • Whitmarsh Alan J

From: Faculty of Life Sciences, University of Manchester, Michael Smith Building, Oxford Road, Manchester, M13 9PT, UK. alan.j.whitmarsh@manchester.ac.uk

Biochimica et biophysica acta

  • Publish Date: Aug 2007
  • ISSN: 0006-3002
  • Volume: 1773
  • Issue: 8
  • Pages: 1285-98
  • Medium: Print
  • Language: English
  • Citation (JAMA): Whitmarsh Alan J, et al. Regulation of Gene Transcription by Mitogen-activated Protein Kinase Signaling Pathways.. Biochim. Biophys. Acta Aug 2007;1773:1285-98

Abstract

Mitogen-activated protein kinase (MAPK) signaling pathways are key mediators of eukaryotic transcriptional responses to extracellular signals. These pathways control gene expression in a number of ways including the phosphorylation and regulation of transcription factors, co-regulatory proteins and chromatin proteins. MAPK pathways therefore target multiple components of transcriptional complexes at gene promoters and can regulate DNA binding, protein stability, cellular localization, transactivation or repression, and nucleosome structure. Recent work has uncovered further complexities in the mechanisms by which MAPKs control gene expression including their roles as integral components of transcription factor complexes and their interplay with other post-translational modification pathways. In this review I discuss these advances with particular focus on how MAPK signals are integrated by transcription factor complexes to provide specific transcriptional responses and how this relates to cellular function.

Mesh Headings (Keywords): Acetylation, Animals, Binding Sites, Extracellular Signal-Regulated MAP Kinases, Humans, MAP Kinase Signaling System, Models, Biological, Multiprotein Complexes, Protein Processing, Post-Translational, Small Ubiquitin-Related Modifier Proteins, Transcription Factors, Transcription, Genetic


Check for Full Text / PubMed Unique Identifier (PMID): 17196680


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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