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NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells

During murine germ cell development, male germ cells enter the mitotically arrested G0 stage, which is an initial step of sexually dimorphic differentiation. The male-specific RNA-binding protein NANOS2 has a key role in suppressing the cell cycle in germ cells. However, the detailed mechanism of ho...

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Detalles Bibliográficos
Autores principales: Shimada, Ryuki, Koike, Hiroko, Hirano, Takamasa, Kato, Yuzuru, Saga, Yumiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350546/
https://www.ncbi.nlm.nih.gov/pubmed/34401671
http://dx.doi.org/10.1016/j.isci.2021.102890
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author Shimada, Ryuki
Koike, Hiroko
Hirano, Takamasa
Kato, Yuzuru
Saga, Yumiko
author_facet Shimada, Ryuki
Koike, Hiroko
Hirano, Takamasa
Kato, Yuzuru
Saga, Yumiko
author_sort Shimada, Ryuki
collection PubMed
description During murine germ cell development, male germ cells enter the mitotically arrested G0 stage, which is an initial step of sexually dimorphic differentiation. The male-specific RNA-binding protein NANOS2 has a key role in suppressing the cell cycle in germ cells. However, the detailed mechanism of how NANOS2 regulates the cell cycle remains unclear. Using single-cell RNA sequencing (scRNA-seq), we extracted the cell cycle state of each germ cell in wild-type and Nanos2-KO testes and revealed that Nanos2 expression starts in mitotic cells and induces mitotic arrest. We identified Rheb, a regulator of mTORC1, and Ptma as possible targets of NANOS2. We propose that repression of the cell cycle is a primary function of NANOS2 and that it is mediated via the suppression of mTORC1 activity through the repression of Rheb in a post-transcriptional manner.
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spelling pubmed-83505462021-08-15 NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells Shimada, Ryuki Koike, Hiroko Hirano, Takamasa Kato, Yuzuru Saga, Yumiko iScience Article During murine germ cell development, male germ cells enter the mitotically arrested G0 stage, which is an initial step of sexually dimorphic differentiation. The male-specific RNA-binding protein NANOS2 has a key role in suppressing the cell cycle in germ cells. However, the detailed mechanism of how NANOS2 regulates the cell cycle remains unclear. Using single-cell RNA sequencing (scRNA-seq), we extracted the cell cycle state of each germ cell in wild-type and Nanos2-KO testes and revealed that Nanos2 expression starts in mitotic cells and induces mitotic arrest. We identified Rheb, a regulator of mTORC1, and Ptma as possible targets of NANOS2. We propose that repression of the cell cycle is a primary function of NANOS2 and that it is mediated via the suppression of mTORC1 activity through the repression of Rheb in a post-transcriptional manner. Elsevier 2021-07-22 /pmc/articles/PMC8350546/ /pubmed/34401671 http://dx.doi.org/10.1016/j.isci.2021.102890 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Shimada, Ryuki
Koike, Hiroko
Hirano, Takamasa
Kato, Yuzuru
Saga, Yumiko
NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells
title NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells
title_full NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells
title_fullStr NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells
title_full_unstemmed NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells
title_short NANOS2 suppresses the cell cycle by repressing mTORC1 activators in embryonic male germ cells
title_sort nanos2 suppresses the cell cycle by repressing mtorc1 activators in embryonic male germ cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8350546/
https://www.ncbi.nlm.nih.gov/pubmed/34401671
http://dx.doi.org/10.1016/j.isci.2021.102890
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