Transcriptional Control by NF-κB: Elongation in Focus

被引:95
作者
Diamant, Gil [1 ]
Dikstein, Rivka [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2013年 / 1829卷 / 09期
基金
以色列科学基金会;
关键词
NF-kappa B; transcription elongation; P-TEFb; Brd4; DSIF; RNA-POLYMERASE-II; IMMUNODEFICIENCY-VIRUS TRANSCRIPTION; SENSITIVITY-INDUCING FACTOR; BROMODOMAIN PROTEIN BRD4; CARBOXY-TERMINAL DOMAIN; TATA-BINDING PROTEIN; P-TEFB; GENE-EXPRESSION; MESSENGER-RNA; TRANSACTIVATION DOMAIN;
D O I
10.1016/j.bbagrm.2013.04.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The NF-kappa B family of transcription factors governs the cellular reaction to a variety of extracellular signals. Following stimulation, NF-kappa B activates genes involved in inflammation, cell survival, cell cycle, immune cell homeostasis and more. This review focuses on studies of the past decade that uncover the transcription elongation process as a key regulatory stage in the activation pathway of NF-kappa B. Of interest are studies that point to the elongation phase as central to the selectivity of target gene activation by NF-kappa B. Particularly, the cascade leading to phosphorylation and acetylation of the NF-kappa B subunit p65 on serine 276 and lysine 310, respectively, was shown to mediate the recruitment of Brd4 and P-TEFb to many pro-inflammatory target genes, which in turn facilitate elongation and mRNA processing. On the other hand, some anti-inflammatory genes are refractory to this pathway and are dependent on the elongation factor DSIF for efficient elongation and rnRNA processing. While these studies have advanced our knowledge of NF-kappa B transcriptional activity, they have also raised unresolved issues regarding the specific genomic and physiological contexts by which NF-kappa B utilizes different mechanisms for activation. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:937 / 945
页数:9
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