A scaffold lncRNA shapes the mitosis to meiosis switch.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
03 02 2021
Historique:
received: 15 07 2020
accepted: 05 01 2021
entrez: 4 2 2021
pubmed: 5 2 2021
medline: 23 2 2021
Statut: epublish

Résumé

Long non-coding RNAs (lncRNAs) contribute to the regulation of gene expression in response to intra- or extracellular signals but the underlying molecular mechanisms remain largely unexplored. Here, we identify an uncharacterized lncRNA as a central player in shaping the meiotic gene expression program in fission yeast. We report that this regulatory RNA, termed mamRNA, scaffolds the antagonistic RNA-binding proteins Mmi1 and Mei2 to ensure their reciprocal inhibition and fine tune meiotic mRNA degradation during mitotic growth. Mechanistically, mamRNA allows Mmi1 to target Mei2 for ubiquitin-mediated downregulation, and conversely enables accumulating Mei2 to impede Mmi1 activity, thereby reinforcing the mitosis to meiosis switch. These regulations also occur within a unique Mmi1-containing nuclear body, positioning mamRNA as a spatially-confined sensor of Mei2 levels. Our results thus provide a mechanistic basis for the mutual control of gametogenesis effectors and further expand our vision of the regulatory potential of lncRNAs.

Identifiants

pubmed: 33536434
doi: 10.1038/s41467-021-21032-7
pii: 10.1038/s41467-021-21032-7
pmc: PMC7859202
doi:

Substances chimiques

Mmi1 protein, S pombe 0
RNA, Fungal 0
RNA, Long Noncoding 0
RNA, Messenger 0
RNA-Binding Proteins 0
Schizosaccharomyces pombe Proteins 0
mRNA Cleavage and Polyadenylation Factors 0
mei2 protein, S pombe 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

770

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Auteurs

Vedrana Andric (V)

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.

Alicia Nevers (A)

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.
University Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, 78350, Jouy-en-Josas, France.

Ditipriya Hazra (D)

Laboratoire de Biologie Structurale de la Cellule (BIOC), CNRS, Ecole polytechnique, Institut Polytechnique de Paris, 91128, Palaiseau, France.
Department of Biochemistry, Oxford University, Oxford, OX1 3QU, UK.

Sylvie Auxilien (S)

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.

Alexandra Menant (A)

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France.

Marc Graille (M)

Laboratoire de Biologie Structurale de la Cellule (BIOC), CNRS, Ecole polytechnique, Institut Polytechnique de Paris, 91128, Palaiseau, France.

Benoit Palancade (B)

Université de Paris, CNRS, Institut Jacques Monod, F-75006, Paris, France.

Mathieu Rougemaille (M)

Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), 91198, Gif-sur-Yvette, France. mathieu.rougemaille@i2bc.paris-saclay.fr.

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Classifications MeSH