Gene repression by coactivator repulsion.

Abstract:

:We show that the IRF-2 oncoprotein represses virus-induced IFN-beta gene transcription via a novel mechanism. Virus infection induces recruitment of IRF-2 to some of the endogenous IFN-beta enhancers as part of the enhanceosome. Enhanceosomes bearing IRF-2 cannot activate transcription, due to the presence of a domain in IRF-2 that prevents enhanceosome-dependent recruitment of the CBP-Pol II holoenzyme complex. As a consequence, IRF-2 incorporation into enhanceosomes restricts the number of IFN-beta promoters directing transcription. Remarkably, deletion of the IRF-2 gene increases IFN-beta expression by expanding the number of cells capable of inducing IFN-beta gene transcription in response to virus infection.

journal_name

Mol Cell

journal_title

Molecular cell

authors

Senger K,Merika M,Agalioti T,Yie J,Escalante CR,Chen G,Aggarwal AK,Thanos D

doi

10.1016/s1097-2765(05)00081-x

subject

Has Abstract

pub_date

2000-10-01 00:00:00

pages

931-7

issue

4

eissn

1097-2765

issn

1097-4164

pii

S1097-2765(05)00081-X

journal_volume

6

pub_type

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