Cargando…

MiR-202 controls female fecundity by regulating medaka oogenesis

Female gamete production relies on coordinated molecular and cellular processes that occur in the ovary throughout oogenesis. In fish, as in other vertebrates, these processes have been extensively studied both in terms of endocrine/paracrine regulation and protein expression and activity. The role...

Descripción completa

Detalles Bibliográficos
Autores principales: Gay, Stéphanie, Bugeon, Jérôme, Bouchareb, Amine, Henry, Laure, Delahaye, Clara, Legeai, Fabrice, Montfort, Jérôme, Le Cam, Aurélie, Siegel, Anne, Bobe, Julien, Thermes, Violette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147661/
https://www.ncbi.nlm.nih.gov/pubmed/30199527
http://dx.doi.org/10.1371/journal.pgen.1007593
_version_ 1783356598637297664
author Gay, Stéphanie
Bugeon, Jérôme
Bouchareb, Amine
Henry, Laure
Delahaye, Clara
Legeai, Fabrice
Montfort, Jérôme
Le Cam, Aurélie
Siegel, Anne
Bobe, Julien
Thermes, Violette
author_facet Gay, Stéphanie
Bugeon, Jérôme
Bouchareb, Amine
Henry, Laure
Delahaye, Clara
Legeai, Fabrice
Montfort, Jérôme
Le Cam, Aurélie
Siegel, Anne
Bobe, Julien
Thermes, Violette
author_sort Gay, Stéphanie
collection PubMed
description Female gamete production relies on coordinated molecular and cellular processes that occur in the ovary throughout oogenesis. In fish, as in other vertebrates, these processes have been extensively studied both in terms of endocrine/paracrine regulation and protein expression and activity. The role of small non-coding RNAs in the regulation of animal reproduction remains however largely unknown and poorly investigated, despite a growing interest for the importance of miRNAs in a wide variety of biological processes. Here, we analyzed the role of miR-202, a miRNA predominantly expressed in male and female gonads in several vertebrate species. We studied its expression in the medaka ovary and generated a mutant line (using CRISPR/Cas9 genome editing) to determine its importance for reproductive success with special interest for egg production. Our results show that miR-202-5p is the most abundant mature form of the miRNA and that it is expressed in granulosa cells and in the unfertilized egg. The knock out (KO) of mir-202 gene resulted in a strong phenotype both in terms of number and quality of eggs produced. Mutant females exhibited either no egg production or produced a dramatically reduced number of eggs that could not be fertilized, ultimately leading to no reproductive success. We quantified the size distribution of the oocytes in the ovary of KO females and performed a large-scale transcriptomic analysis approach to identified dysregulated molecular pathways. Together, cellular and molecular analyses indicate that the lack of miR-202 impairs the early steps of oogenesis/folliculogenesis and decreases the number of large (i.e. vitellogenic) follicles, ultimately leading to dramatically reduced female fecundity. This study sheds new light on the regulatory mechanisms that control the early steps of follicular development, including possible targets of miR-202-5p, and provides the first in vivo functional evidence that a gonad-predominant microRNA may have a major role in female reproduction.
format Online
Article
Text
id pubmed-6147661
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-61476612018-10-08 MiR-202 controls female fecundity by regulating medaka oogenesis Gay, Stéphanie Bugeon, Jérôme Bouchareb, Amine Henry, Laure Delahaye, Clara Legeai, Fabrice Montfort, Jérôme Le Cam, Aurélie Siegel, Anne Bobe, Julien Thermes, Violette PLoS Genet Research Article Female gamete production relies on coordinated molecular and cellular processes that occur in the ovary throughout oogenesis. In fish, as in other vertebrates, these processes have been extensively studied both in terms of endocrine/paracrine regulation and protein expression and activity. The role of small non-coding RNAs in the regulation of animal reproduction remains however largely unknown and poorly investigated, despite a growing interest for the importance of miRNAs in a wide variety of biological processes. Here, we analyzed the role of miR-202, a miRNA predominantly expressed in male and female gonads in several vertebrate species. We studied its expression in the medaka ovary and generated a mutant line (using CRISPR/Cas9 genome editing) to determine its importance for reproductive success with special interest for egg production. Our results show that miR-202-5p is the most abundant mature form of the miRNA and that it is expressed in granulosa cells and in the unfertilized egg. The knock out (KO) of mir-202 gene resulted in a strong phenotype both in terms of number and quality of eggs produced. Mutant females exhibited either no egg production or produced a dramatically reduced number of eggs that could not be fertilized, ultimately leading to no reproductive success. We quantified the size distribution of the oocytes in the ovary of KO females and performed a large-scale transcriptomic analysis approach to identified dysregulated molecular pathways. Together, cellular and molecular analyses indicate that the lack of miR-202 impairs the early steps of oogenesis/folliculogenesis and decreases the number of large (i.e. vitellogenic) follicles, ultimately leading to dramatically reduced female fecundity. This study sheds new light on the regulatory mechanisms that control the early steps of follicular development, including possible targets of miR-202-5p, and provides the first in vivo functional evidence that a gonad-predominant microRNA may have a major role in female reproduction. Public Library of Science 2018-09-10 /pmc/articles/PMC6147661/ /pubmed/30199527 http://dx.doi.org/10.1371/journal.pgen.1007593 Text en © 2018 Gay et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gay, Stéphanie
Bugeon, Jérôme
Bouchareb, Amine
Henry, Laure
Delahaye, Clara
Legeai, Fabrice
Montfort, Jérôme
Le Cam, Aurélie
Siegel, Anne
Bobe, Julien
Thermes, Violette
MiR-202 controls female fecundity by regulating medaka oogenesis
title MiR-202 controls female fecundity by regulating medaka oogenesis
title_full MiR-202 controls female fecundity by regulating medaka oogenesis
title_fullStr MiR-202 controls female fecundity by regulating medaka oogenesis
title_full_unstemmed MiR-202 controls female fecundity by regulating medaka oogenesis
title_short MiR-202 controls female fecundity by regulating medaka oogenesis
title_sort mir-202 controls female fecundity by regulating medaka oogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6147661/
https://www.ncbi.nlm.nih.gov/pubmed/30199527
http://dx.doi.org/10.1371/journal.pgen.1007593
work_keys_str_mv AT gaystephanie mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT bugeonjerome mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT boucharebamine mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT henrylaure mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT delahayeclara mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT legeaifabrice mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT montfortjerome mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT lecamaurelie mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT siegelanne mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT bobejulien mir202controlsfemalefecunditybyregulatingmedakaoogenesis
AT thermesviolette mir202controlsfemalefecunditybyregulatingmedakaoogenesis