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RNA聚合酶II在染色质模板上的延伸需要拓扑异构酶活性。

Elongation by RNA polymerase II on chromatin templates requires topoisomerase activity.

作者信息

Mondal Neelima, Zhang Ye, Jonsson Zophonias, Dhar Suman Kumar, Kannapiran Madhu, Parvin Jeffrey D

机构信息

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Nucleic Acids Res. 2003 Sep 1;31(17):5016-24. doi: 10.1093/nar/gkg705.

Abstract

Transcription on chromatin by RNA polymerase II (pol II) is repressed as compared with transcription on histone-free DNA. In this study, we show that human topoisomerase I (topo I) and yeast topoisomerase II (topo II), each of which relax both positive and negative superhelical tension, reverse the transcriptional repression by chromatin. In the presence of bacterial topo I, which can relax only negative superhelical tension, the transcription is repressed on chromatin templates. The data together show that the relaxation of positive superhelical tension by these enzymes was the key property required for RNA synthesis from chromatin templates. In the absence of topoisomerase, transcriptional repression on chromatin depended on RNA length. The synthesis of transcripts of 100 nt or shorter was unaffected by chromatin, but repression was apparent when the RNA transcript was 200 nt or longer. These findings suggest that transcription on chromatin templates results in the accumulation of positive superhelical tension by the elongating polymerase, which in turn inhibits further elongation in the absence of topoisomerase activity.

摘要

与在无组蛋白的DNA上进行转录相比,RNA聚合酶II(pol II)在染色质上的转录受到抑制。在本研究中,我们表明,人类拓扑异构酶I(topo I)和酵母拓扑异构酶II(topo II),它们均可缓解正超螺旋和负超螺旋张力,能逆转染色质对转录的抑制作用。在仅能缓解负超螺旋张力的细菌拓扑异构酶I存在的情况下,染色质模板上的转录受到抑制。这些数据共同表明,这些酶对正超螺旋张力的缓解是从染色质模板进行RNA合成所需的关键特性。在没有拓扑异构酶的情况下,染色质上的转录抑制取决于RNA长度。100个核苷酸或更短的转录本合成不受染色质影响,但当RNA转录本为200个核苷酸或更长时,抑制作用明显。这些发现表明,染色质模板上的转录会导致延伸中的聚合酶积累正超螺旋张力,进而在缺乏拓扑异构酶活性的情况下抑制进一步延伸。

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本文引用的文献

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Transcriptional consequences of topoisomerase inhibition.拓扑异构酶抑制的转录后果。
Mol Cell Biol. 2001 Dec;21(24):8437-51. doi: 10.1128/MCB.21.24.8437-8451.2001.

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