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Chromatin-bound mitogen-activated protein kinases transmit dynamic signals in transcription complexes in β-cells
Author(s) -
Michael C. Lawrence,
Kathleen McGlynn,
Chunli Shao,
Lingling Duan,
Bashoo Naziruddin,
Marlon F. Levy,
Melanie H. Cobb
Publication year - 2008
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0806465105
Subject(s) - promoter , response element , transcription factor , transcription (linguistics) , e box , biology , mapk/erk pathway , general transcription factor , activating transcription factor 2 , microbiology and biotechnology , sp3 transcription factor , creb1 , repressor , rna polymerase ii , gene , kinase , gene expression , genetics , creb , linguistics , philosophy
MAPK pathways regulate transcription through phosphorylation of transcription factors and other DNA-binding proteins. In pancreatic beta-cells, ERK1/2 are required for transcription of the insulin gene and several other genes in response to glucose. We show that binding of glucose-sensitive transcription activators and repressors to the insulin gene promoter depends on ERK1/2 activity. We also find that glucose and NGF stimulate the binding of ERK1/2 to the insulin gene and other promoters. An ERK1/2 cascade module, including MEK1/2 and Rsk, are found in complexes bound to these promoters. These findings imply that MAPK-containing signaling complexes are positioned on sensitive promoters with their protein substrates to modulate transcription in situ in response to incoming signals.

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