Stowers Institute for Medical Research, Kansas City, Missouri, USA.
Mol Cell Biol. 2012 Jul;32(13):2608-17. doi: 10.1128/MCB.00182-12. Epub 2012 Apr 30.
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.
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。