Non-coding 7S RNA inhibits transcription via mitochondrial RNA polymerase dimerization

被引:32
|
作者
Zhu, Xuefeng [1 ]
Xie, Xie [1 ]
Das, Hrishikesh [2 ]
Tan, Benedict G. [1 ]
Shi, Yonghong [1 ]
Al-Behadili, Ali [1 ]
Peter, Bradley [1 ]
Motori, Elisa [3 ,4 ]
Valenzuela, Sebastian [1 ]
Posse, Viktor [1 ]
Gustafsson, Claes M. [1 ]
Haellberg, B. Martin [2 ]
Falkenberg, Maria [1 ]
机构
[1] Univ Gothenburg, Dept Med Biochem & Cell Biol, POB 440, S-40530 Gothenburg, Sweden
[2] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
[3] Cologne Excellence Cluster Cellular Stress Respon, D-50931 Cologne, Germany
[4] Univ Cologne, Inst Biochem, Zulpicher Str 47, D-50674 Cologne, Germany
基金
瑞典研究理事会; 欧洲研究理事会;
关键词
DOUBLE-STRANDED-RNA; DNA-REPLICATION; CRYO-EM; POLYNUCLEOTIDE PHOSPHORYLASE; STRUCTURAL BASIS; B2; RNA; 6S RNA; IDENTIFICATION; EXPRESSION; INITIATION;
D O I
10.1016/j.cell.2022.05.006
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 mitochondrial genome encodes 13 components of the oxidative phosphorylation system, and altered mitochondrial transcription drives various human pathologies. A polyadenylated, non-coding RNA molecule known as 7S RNA is transcribed from a region immediately downstream of the light strand promoter in mammalian cells, and its levels change rapidly in response to physiological conditions. Here, we report that 7S RNA has a regulatory function, as it controls levels of mitochondrial transcription both in vitro and in cultured human cells. Using cryo-EM, we show that POLRMT dimerization is induced by interactions with 7S RNA. The resulting POLRMT dimer interface sequesters domains necessary for promoter recognition and unwinding, thereby preventing transcription initiation. We propose that the non-coding 7S RNA molecule is a component of a negative feedback loop that regulates mitochondrial transcription in mammalian cells.
引用
收藏
页码:2309 / +
页数:40
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