The tRNA-like small noncoding RNA mascRNA promotes global protein translation.


Journal

EMBO reports
ISSN: 1469-3178
Titre abrégé: EMBO Rep
Pays: England
ID NLM: 100963049

Informations de publication

Date de publication:
03 12 2020
Historique:
received: 14 11 2019
revised: 16 09 2020
accepted: 21 09 2020
pubmed: 20 10 2020
medline: 28 4 2021
entrez: 19 10 2020
Statut: ppublish

Résumé

mascRNA is a small cytoplasmic RNA derived from the lncRNA MALAT1. After being processed by the tRNA processing enzymes RNase P and RNase Z, mascRNA undergoes CCA addition like tRNAs and folds into a tRNA-like cloverleaf structure. While MALAT1 functions in multiple cellular processes, the role of mascRNA was largely unknown. Here, we show that mascRNA binds directly to the multi-tRNA synthetase complex (MSC) component glutaminyl-tRNA synthetase (QARS). mascRNA promotes global protein translation and cell proliferation by positively regulating QARS protein levels. Our results uncover a role of mascRNA that is independent of MALAT1, but could be part of the molecular mechanism of MALAT1's function in cancer, and provide a paradigm for understanding tRNA-like structures in mammalian cells.

Identifiants

pubmed: 33073493
doi: 10.15252/embr.201949684
pmc: PMC7726780
doi:

Substances chimiques

RNA, Long Noncoding 0
RNA, Small Untranslated 0
RNA, Transfer 9014-25-9

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e49684

Subventions

Organisme : Ministry of Science and Technology of the People's Republic of China (MOST)
ID : 2017YFA0504600
Organisme : National Natural Science Foundation of China (NSFC)
ID : 91949103
Organisme : National Natural Science Foundation of China (NSFC)
ID : 91649103

Informations de copyright

© 2020 The Authors.

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Auteurs

Xinping Lu (X)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.

Jinliang Huang (J)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.

Sipeng Wu (S)

State Key laboratory for Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Fujian, China.

Qian Zheng (Q)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.

Peipei Liu (P)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.

Huimin Feng (H)

State Key laboratory for Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Fujian, China.

Xiaoqing Su (X)

State Key laboratory for Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Fujian, China.

Haipeng Fu (H)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.

Qiaoran Xi (Q)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.

Geng Wang (G)

MOE Key laboratory of Bioinformatics, Cell Biology and Development Center, School of Life Sciences, Tsinghua University, Beijing, China.
State Key laboratory for Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Fujian, China.

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