The Super Elongation Complex Family of RNA Polymerase II Elongation Factors: Gene Target Specificity and Transcriptional Output

被引:148
作者
Luo, Zhuojuan [1 ]
Lin, Chengqi [1 ]
Guest, Erin [1 ]
Garrett, Alexander S. [1 ]
Mohaghegh, Nima [1 ]
Swanson, Selene [1 ]
Marshall, Stacy [1 ]
Florens, Laurence [1 ]
Washburn, Michael P. [1 ,2 ]
Shilatifard, All [1 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO USA
[2] Univ Kansas, Med Ctr, Dept Pathol & Lab Med, Kansas City, KS 66103 USA
基金
美国国家卫生研究院;
关键词
BROMODOMAIN PROTEIN BRD4; P-TEFB; HUMAN GENOME; HIV-1; TAT; IN-VIVO; C-MYC; MLL; CHROMATIN; LEUKEMIA; RECRUITMENT;
D O I
10.1128/MCB.00182-12
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 elongation stage of transcription is highly regulated in metazoans. We previously purified the AFF1- and AFF4-containing super elongation complex (SEC) as a major regulator of development and cancer pathogenesis. Here, we report the biochemical isolation of SEC-like 2 (SEC-L2) and SEC-like 3 (SEC-L3) containing AFF2 and AFF3 in association with P-TEFb, ENL/MLLT1, and AF9/MLLT3. The SEC family members demonstrate high levels of polymerase II (Poll II) C-terminal domain kinase activity; however, only SEC is required for the proper induction of the HSP70 gene upon stress. Genome-wide mRNA-Seq analyses demonstrated that SEC-L2 and SEC-L3 control the expression of different subsets of genes, while AFF4/SEC plays a more dominant role in rapid transcriptional induction in cells. MYC is one of the direct targets of AFF4/SEC, and SEC recruitment to the MYC gene regulates its expression in different cancer cells, including those in acute myeloid or lymphoid leukemia. These findings suggest that AFF4/SEC could be a potential therapeutic target for the treatment of leukemia or other cancers associated with MYC overexpression.
引用
收藏
页码:2608 / 2617
页数:10
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