Dynamic changes in transcription factor complexes during erythroid differentiation revealed by quantitative proteomics View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-12-29

AUTHORS

Marjorie Brand, Jeffrey A Ranish, Nicolas T Kummer, Joan Hamilton, Kazuhiko Igarashi, Claire Francastel, Tian H Chi, Gerald R Crabtree, Ruedi Aebersold, Mark Groudine

ABSTRACT

During erythroid differentiation, β-globin gene expression is regulated by the locus control region (LCR). The transcription factor NF-E2p18/MafK binds within this region and is essential for β-globin expression in murine erythroleukemia (MEL) cells. Here we use the isotope-coded affinity tag (ICAT) technique of quantitative mass spectrometry to compare proteins interacting with NF-E2p18/MafK during differentiation. Our results define MafK as a 'dual-function' molecule that shifts from a repressive to an activating mode during erythroid differentiation. The exchange of MafK dimerization partner from Bach1 to NF-E2p45 is a key step in the switch from the repressed to the active state. This shift is associated with changes in the interaction of MafK with co-repressors and co-activators. Thus, our results suggest that in addition to its role as a cis-acting activator of β-globin gene expression in differentiated erythroid cells, the LCR also promotes an active repression of β-globin transcription in committed cells before terminal differentiation. More... »

PAGES

73-80

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/nsmb713

DOI

http://dx.doi.org/10.1038/nsmb713

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1031228962

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/14718926


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