Literature DB >> 16083290

Identification of novel and cell type enriched cofactors of the transcription activation domain of RelA (p65 NF-kappaB).

Heather R Owen1, Manfredo Quadroni, Willy Bienvenut, Christine Buerki, Michael O Hottiger.   

Abstract

RelA (NF-kappaB) is a transcription factor inducible by distinct stimuli in many different cell types. To find new cell type specific cofactors of NF-kappaB dependent transcription, we isolated RelA transcription activation domain binding proteins from the nuclear extracts of three different cell types. Analysis by electrophoresis and liquid chromatography tandem mass spectrometry identified several novel putative molecular partners. Some were strongly enriched in the complex formed from the nuclear extracts of specific cell types.

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Year:  2005        PMID: 16083290     DOI: 10.1021/pr0500713

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  2 in total

1.  Phosphorylation of p65(RelA) on Ser(547) by ATM represses NF-κB-dependent transcription of specific genes after genotoxic stress.

Authors:  Hélène Sabatel; Emmanuel Di Valentin; Geoffrey Gloire; Franck Dequiedt; Jacques Piette; Yvette Habraken
Journal:  PLoS One       Date:  2012-06-08       Impact factor: 3.240

2.  SIMPL enhancement of tumor necrosis factor-α dependent p65-MED1 complex formation is required for mammalian hematopoietic stem and progenitor cell function.

Authors:  Weina Zhao; Erin Breese; Allison Bowers; Jonathan Hoggatt; Louis M Pelus; Hal E Broxmeyer; Mark Goebl; Maureen A Harrington
Journal:  PLoS One       Date:  2013-04-22       Impact factor: 3.240

  2 in total

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