The Role of c-Jun N-Terminal Kinase, p38, and Extracellular Signal-Regulated Kinase in Insulin-Induced Thr69 and Thr71 Phosphorylation of Activating Transcription Factor 2-Reference-Cited by-同舟云学术

The Role of c-Jun N-Terminal Kinase, p38, and Extracellular Signal-Regulated Kinase in Insulin-Induced Thr69 and Thr71 Phosphorylation of Activating Transcription Factor 2

Published:2006-08-01 Issue:8 Volume:20 Page:1786-1795
ISSN:0888-8809
Container-title:Molecular Endocrinology
language:en
Short-container-title:

Author:

Baan Bart¹,van Dam Hans¹,van der Zon Gerard C. M.¹,Maassen J. Antonie¹,Ouwens D. Margriet¹

Affiliation:

1. Department of Molecular Cell Biology, Section Signal Transduction and Ageing, Leiden University Medical Centre, 2300 RC Leiden, The Netherlands

Publisher

The Endocrine Society

Subject

Endocrinology,Molecular Biology,General Medicine

Link

http://academic.oup.com/mend/article-pdf/20/8/1786/8956671/mend1786.pdf

Reference32 articles.

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2. Growth factors can activate ATF2 via a two-step mechanism: phosphorylation of Thr71 through the Ras-MEK-ERK pathway and of Thr69 through RalGDS-Src-p38.;Ouwens;EMBO J,2002

3. Transcriptional regulation by the phosphorylation-dependent factor CREB.;Mayr;Nat Rev Mol Cell Biol,2001

4. The molecular biology and nomenclature of the activating transcription factor/cAMP responsive element binding family of transcription factors: activating transcription factor proteins and homeostasis.;Hai;Gene,2001

5. Transcription factor ATF cDNA clones: an extensive family of leucine zipper proteins able to selectively form DNA-binding heterodimers.;Hai;Genes Dev,1989

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