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本文引用的文献

1
Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia.抑制 BET 募集到染色质可作为治疗 MLL 融合白血病的有效方法。
Nature. 2011 Oct 2;478(7370):529-33. doi: 10.1038/nature10509.
2
BET bromodomain inhibition as a therapeutic strategy to target c-Myc.BET 溴结构域抑制作为靶向 c-Myc 的治疗策略。
Cell. 2011 Sep 16;146(6):904-17. doi: 10.1016/j.cell.2011.08.017. Epub 2011 Sep 1.
3
Human Polymerase-Associated Factor complex (PAFc) connects the Super Elongation Complex (SEC) to RNA polymerase II on chromatin.人类聚合酶相关因子复合物(PAFc)将超级延伸复合物(SEC)连接到染色质上的 RNA 聚合酶 II。
Proc Natl Acad Sci U S A. 2011 Sep 6;108(36):E636-45. doi: 10.1073/pnas.1107107108. Epub 2011 Aug 22.
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RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia.RNAi 筛选鉴定 Brd4 为急性髓系白血病的治疗靶点。
Nature. 2011 Aug 3;478(7370):524-8. doi: 10.1038/nature10334.
5
Dynamic transcriptional events in embryonic stem cells mediated by the super elongation complex (SEC).由超级延伸复合物(SEC)介导的胚胎干细胞中的动态转录事件。
Genes Dev. 2011 Jul 15;25(14):1486-98. doi: 10.1101/gad.2059211.
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Human mediator subunit MED26 functions as a docking site for transcription elongation factors.人类中介体亚基 MED26 作为转录延伸因子的对接位点发挥作用。
Cell. 2011 Jul 8;146(1):92-104. doi: 10.1016/j.cell.2011.06.005.
7
The super elongation complex (SEC) and MLL in development and disease.超级延伸复合物(SEC)和 MLL 在发育和疾病中的作用。
Genes Dev. 2011 Apr 1;25(7):661-72. doi: 10.1101/gad.2015411.
8
New insights into the control of HIV-1 transcription: when Tat meets the 7SK snRNP and super elongation complex (SEC).HIV-1 转录调控的新见解:当 Tat 遇见 7SK snRNP 和超延伸复合物(SEC)。
J Neuroimmune Pharmacol. 2011 Jun;6(2):260-8. doi: 10.1007/s11481-011-9267-6. Epub 2011 Mar 1.
9
Licensed to elongate: a molecular mechanism for MLL-based leukaemogenesis.获准延长:基于 MLL 的白血病发生的分子机制。
Nat Rev Cancer. 2010 Oct;10(10):721-8. doi: 10.1038/nrc2915. Epub 2010 Sep 16.
10
HIV-1 Tat assembles a multifunctional transcription elongation complex and stably associates with the 7SK snRNP.HIV-1 Tat 组装多功能转录延伸复合物,并与 7SK snRNP 稳定结合。
Mol Cell. 2010 May 14;38(3):439-51. doi: 10.1016/j.molcel.2010.04.012.

RNA 聚合酶 II 延伸因子的超延伸复合物家族:基因靶标特异性和转录输出。

The super elongation complex family of RNA polymerase II elongation factors: gene target specificity and transcriptional output.

机构信息

Stowers Institute for Medical Research, Kansas City, Missouri, USA.

出版信息

Mol Cell Biol. 2012 Jul;32(13):2608-17. doi: 10.1128/MCB.00182-12. Epub 2012 Apr 30.

DOI:10.1128/MCB.00182-12
PMID:22547686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3434493/
Abstract

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 (Pol 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.

摘要

真核生物中转录的延伸阶段受到高度调控。我们之前已经纯化了包含 AFF1 和 AFF4 的超延伸复合物(SEC),它是发育和癌症发病机制的主要调节剂。在这里,我们报告了 SEC 样 2(SEC-L2)和 SEC 样 3(SEC-L3)的生化分离,它们与 P-TEFb、ENL/MLLT1 和 AF9/MLLT3 相关联,其中包含 AFF2 和 AFF3。SEC 家族成员表现出高水平的聚合酶 II(Pol II)C 端结构域激酶活性;然而,只有 SEC 对于应激时正确诱导 HSP70 基因的表达是必需的。全基因组 mRNA-Seq 分析表明,SEC-L2 和 SEC-L3 控制不同基因子集的表达,而 AFF4/SEC 在细胞中快速转录诱导中起更主导作用。MYC 是 AFF4/SEC 的直接靶标之一,SEC 募集到 MYC 基因调节其在不同癌细胞中的表达,包括急性髓细胞或淋巴细胞白血病中的表达。这些发现表明,AFF4/SEC 可能是治疗与 MYC 过表达相关的白血病或其他癌症的潜在治疗靶点。