Cargando…
A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka
Dmrt1 is a highly conserved transcription factor, which is critically involved in regulation of gonad development of vertebrates. In medaka, a duplicate of dmrt1—acting as master sex-determining gene—has a tightly timely and spatially controlled gonadal expression pattern. In addition to transcripti...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448818/ https://www.ncbi.nlm.nih.gov/pubmed/30947255 http://dx.doi.org/10.1371/journal.pbio.3000185 |
_version_ | 1783408728756715520 |
---|---|
author | Herpin, Amaury Schmidt, Cornelia Kneitz, Susanne Gobé, Clara Regensburger, Martina Le Cam, Aurélie Montfort, Jérome Adolfi, Mateus C. Lillesaar, Christina Wilhelm, Dagmar Kraeussling, Michael Mourot, Brigitte Porcon, Béatrice Pannetier, Maëlle Pailhoux, Eric Ettwiller, Laurence Dolle, Dirk Guiguen, Yann Schartl, Manfred |
author_facet | Herpin, Amaury Schmidt, Cornelia Kneitz, Susanne Gobé, Clara Regensburger, Martina Le Cam, Aurélie Montfort, Jérome Adolfi, Mateus C. Lillesaar, Christina Wilhelm, Dagmar Kraeussling, Michael Mourot, Brigitte Porcon, Béatrice Pannetier, Maëlle Pailhoux, Eric Ettwiller, Laurence Dolle, Dirk Guiguen, Yann Schartl, Manfred |
author_sort | Herpin, Amaury |
collection | PubMed |
description | Dmrt1 is a highly conserved transcription factor, which is critically involved in regulation of gonad development of vertebrates. In medaka, a duplicate of dmrt1—acting as master sex-determining gene—has a tightly timely and spatially controlled gonadal expression pattern. In addition to transcriptional regulation, a sequence motif in the 3′ UTR (D3U-box) mediates transcript stability of dmrt1 mRNAs from medaka and other vertebrates. We show here that in medaka, two RNA-binding proteins with antagonizing properties target this D3U-box, promoting either RNA stabilization in germ cells or degradation in the soma. The D3U-box is also conserved in other germ-cell transcripts, making them responsive to the same RNA binding proteins. The evolutionary conservation of the D3U-box motif within dmrt1 genes of metazoans—together with preserved expression patterns of the targeting RNA binding proteins in subsets of germ cells—suggest that this new mechanism for controlling RNA stability is not restricted to fishes but might also apply to other vertebrates. |
format | Online Article Text |
id | pubmed-6448818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64488182019-04-19 A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka Herpin, Amaury Schmidt, Cornelia Kneitz, Susanne Gobé, Clara Regensburger, Martina Le Cam, Aurélie Montfort, Jérome Adolfi, Mateus C. Lillesaar, Christina Wilhelm, Dagmar Kraeussling, Michael Mourot, Brigitte Porcon, Béatrice Pannetier, Maëlle Pailhoux, Eric Ettwiller, Laurence Dolle, Dirk Guiguen, Yann Schartl, Manfred PLoS Biol Research Article Dmrt1 is a highly conserved transcription factor, which is critically involved in regulation of gonad development of vertebrates. In medaka, a duplicate of dmrt1—acting as master sex-determining gene—has a tightly timely and spatially controlled gonadal expression pattern. In addition to transcriptional regulation, a sequence motif in the 3′ UTR (D3U-box) mediates transcript stability of dmrt1 mRNAs from medaka and other vertebrates. We show here that in medaka, two RNA-binding proteins with antagonizing properties target this D3U-box, promoting either RNA stabilization in germ cells or degradation in the soma. The D3U-box is also conserved in other germ-cell transcripts, making them responsive to the same RNA binding proteins. The evolutionary conservation of the D3U-box motif within dmrt1 genes of metazoans—together with preserved expression patterns of the targeting RNA binding proteins in subsets of germ cells—suggest that this new mechanism for controlling RNA stability is not restricted to fishes but might also apply to other vertebrates. Public Library of Science 2019-04-04 /pmc/articles/PMC6448818/ /pubmed/30947255 http://dx.doi.org/10.1371/journal.pbio.3000185 Text en © 2019 Herpin 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 Herpin, Amaury Schmidt, Cornelia Kneitz, Susanne Gobé, Clara Regensburger, Martina Le Cam, Aurélie Montfort, Jérome Adolfi, Mateus C. Lillesaar, Christina Wilhelm, Dagmar Kraeussling, Michael Mourot, Brigitte Porcon, Béatrice Pannetier, Maëlle Pailhoux, Eric Ettwiller, Laurence Dolle, Dirk Guiguen, Yann Schartl, Manfred A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
title | A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
title_full | A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
title_fullStr | A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
title_full_unstemmed | A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
title_short | A novel evolutionary conserved mechanism of RNA stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
title_sort | novel evolutionary conserved mechanism of rna stability regulates synexpression of primordial germ cell-specific genes prior to the sex-determination stage in medaka |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6448818/ https://www.ncbi.nlm.nih.gov/pubmed/30947255 http://dx.doi.org/10.1371/journal.pbio.3000185 |
work_keys_str_mv | AT herpinamaury anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT schmidtcornelia anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT kneitzsusanne anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT gobeclara anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT regensburgermartina anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT lecamaurelie anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT montfortjerome anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT adolfimateusc anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT lillesaarchristina anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT wilhelmdagmar anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT kraeusslingmichael anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT mourotbrigitte anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT porconbeatrice anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT pannetiermaelle anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT pailhouxeric anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT ettwillerlaurence anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT dolledirk anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT guiguenyann anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT schartlmanfred anovelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT herpinamaury novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT schmidtcornelia novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT kneitzsusanne novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT gobeclara novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT regensburgermartina novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT lecamaurelie novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT montfortjerome novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT adolfimateusc novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT lillesaarchristina novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT wilhelmdagmar novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT kraeusslingmichael novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT mourotbrigitte novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT porconbeatrice novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT pannetiermaelle novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT pailhouxeric novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT ettwillerlaurence novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT dolledirk novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT guiguenyann novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka AT schartlmanfred novelevolutionaryconservedmechanismofrnastabilityregulatessynexpressionofprimordialgermcellspecificgenespriortothesexdeterminationstageinmedaka |