共 108 条
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.
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页码:937 / 945
页数:9
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