Litcius/Paper detail

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

Xuefeng Zhu, Xie Xie, Hrishikesh Das, Benedict G. Tan, Yonghong Shi, Ali Al-Behadili, Bradley Peter, Elisa Motori, Sebastian Valenzuela, Viktor Posse, Claes M. Gustafsson, B.M. Hallberg, Maria Falkenberg

2022Cell65 citationsDOIOpen Access PDF

Abstract

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.

Topics & Concepts

BiologyTranscription (linguistics)RNARNA polymerase IICell biologyNon-coding RNAMolecular biologyPolyadenylationRNA polymerase II holoenzymeRNA-dependent RNA polymeraseGenePromoterGeneticsGene expressionPhilosophyLinguisticsRNA modifications and cancerRNA and protein synthesis mechanismsMitochondrial Function and Pathology