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人类整合因子复合物通过内切核酸酶切割新生转录本促进转录延伸。

The Human Integrator Complex Facilitates Transcriptional Elongation by Endonucleolytic Cleavage of Nascent Transcripts.

机构信息

University of Miami Miller School of Medicine, Sylvester Comprehensive Cancer Center, Department of Human Genetics, Biomedical Research Building, Room 719, 1501 NW 10(th) Avenue, Miami, FL 33136, USA.

University of Miami Miller School of Medicine, Sylvester Comprehensive Cancer Center, Department of Human Genetics, Biomedical Research Building, Room 719, 1501 NW 10(th) Avenue, Miami, FL 33136, USA; Medical Scientist Training Program and Graduate Program in Cancer Biology, University of Miami Miller School of Medicine, Miami, FL, USA.

出版信息

Cell Rep. 2020 Jul 21;32(3):107917. doi: 10.1016/j.celrep.2020.107917.

Abstract

Transcription by RNA polymerase II (RNAPII) is pervasive in the human genome. However, the mechanisms controlling transcription at promoters and enhancers remain enigmatic. Here, we demonstrate that Integrator subunit 11 (INTS11), the catalytic subunit of the Integrator complex, regulates transcription at these loci through its endonuclease activity. Promoters of genes require INTS11 to cleave nascent transcripts associated with paused RNAPII and induce their premature termination in the proximity of the +1 nucleosome. The turnover of RNAPII permits the subsequent recruitment of an elongation-competent RNAPII complex, leading to productive elongation. In contrast, enhancers require INTS11 catalysis not to evict paused RNAPII but rather to terminate enhancer RNA transcription beyond the +1 nucleosome. These findings are supported by the differential occupancy of negative elongation factor (NELF), SPT5, and tyrosine-1-phosphorylated RNAPII. This study elucidates the role of Integrator in mediating transcriptional elongation at human promoters through the endonucleolytic cleavage of nascent transcripts and the dynamic turnover of RNAPII.

摘要

RNA 聚合酶 II(RNAPII)的转录在人类基因组中普遍存在。然而,控制启动子和增强子转录的机制仍然很神秘。在这里,我们证明了整合子亚基 11(INTS11),即整合酶复合物的催化亚基,通过其内切酶活性调节这些基因座的转录。基因启动子需要 INTS11 来切割与暂停的 RNAPII 相关的新生转录本,并在 +1 核小体附近诱导其过早终止。RNAPII 的周转允许随后招募具有延伸能力的 RNAPII 复合物,从而导致有效的延伸。相比之下,增强子需要 INTS11 催化作用不是驱逐暂停的 RNAPII,而是终止增强子 RNA 转录超出 +1 核小体。这些发现得到了负延伸因子(NELF)、SPT5 和酪氨酸 1 磷酸化 RNAPII 差异占有率的支持。这项研究阐明了整合子在通过新生转录本的内切酶切割和 RNAPII 的动态周转介导人类启动子转录延伸中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de9/7427568/8864c611d552/nihms-1613941-f0002.jpg

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