Cargando…

MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo

In the sea urchin embryo, specification of the dorsal-ventral axis critically relies on the spatially restricted expression of nodal in the presumptive ventral ectoderm. The ventral restriction of nodal expression requires the activity of the maternal TGF-β ligand Panda but the mechanism by which Pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Molina, M. Dolores, Quirin, Magali, Haillot, Emmanuel, De Crozé, Noémie, Range, Ryan, Rouel, Mathieu, Jimenez, Felipe, Amrouche, Radja, Chessel, Aline, Lepage, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160229/
https://www.ncbi.nlm.nih.gov/pubmed/30222786
http://dx.doi.org/10.1371/journal.pgen.1007621
_version_ 1783358729991749632
author Molina, M. Dolores
Quirin, Magali
Haillot, Emmanuel
De Crozé, Noémie
Range, Ryan
Rouel, Mathieu
Jimenez, Felipe
Amrouche, Radja
Chessel, Aline
Lepage, Thierry
author_facet Molina, M. Dolores
Quirin, Magali
Haillot, Emmanuel
De Crozé, Noémie
Range, Ryan
Rouel, Mathieu
Jimenez, Felipe
Amrouche, Radja
Chessel, Aline
Lepage, Thierry
author_sort Molina, M. Dolores
collection PubMed
description In the sea urchin embryo, specification of the dorsal-ventral axis critically relies on the spatially restricted expression of nodal in the presumptive ventral ectoderm. The ventral restriction of nodal expression requires the activity of the maternal TGF-β ligand Panda but the mechanism by which Panda restricts nodal expression is unknown. Similarly, what initiates expression of nodal in the ectoderm and what are the mechanisms that link patterning along the primary and secondary axes is not well understood. We report that in Paracentrotus lividus, the activity of the maternally expressed ETS-domain transcription factor Yan/Tel is essential for the spatial restriction of nodal. Inhibiting translation of maternal yan/tel mRNA disrupted dorsal-ventral patterning in all germ layers by causing a massive ectopic expression of nodal starting from cleavage stages, mimicking the phenotype caused by inactivation of the maternal Nodal antagonist Panda. We show that like in the fly or in vertebrates, the activity of sea urchin Yan/Tel is regulated by phosphorylation by MAP kinases. However, unlike in the fly or in vertebrates, phosphorylation by GSK3 plays a central role in the regulation Yan/Tel stability in the sea urchin. We show that GSK3 phosphorylates Yan/Tel in vitro at two different sites including a β-TRCP ubiquitin ligase degradation motif and a C-terminal Ser/Thr rich cluster and that phosphorylation of Yan/Tel by GSK3 triggers its degradation by a β-TRCP/proteasome pathway. Finally, we show that, Yan is epistatic to Panda and that the activity of Yan/Tel is required downstream of Panda to restrict nodal expression. Our results identify Yan/Tel as a central regulator of the spatial expression of nodal in Paracentrotus lividus and uncover a key interaction between the gene regulatory networks responsible for patterning the embryo along the dorsal-ventral and animal-vegetal axes.
format Online
Article
Text
id pubmed-6160229
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-61602292018-10-19 MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo Molina, M. Dolores Quirin, Magali Haillot, Emmanuel De Crozé, Noémie Range, Ryan Rouel, Mathieu Jimenez, Felipe Amrouche, Radja Chessel, Aline Lepage, Thierry PLoS Genet Research Article In the sea urchin embryo, specification of the dorsal-ventral axis critically relies on the spatially restricted expression of nodal in the presumptive ventral ectoderm. The ventral restriction of nodal expression requires the activity of the maternal TGF-β ligand Panda but the mechanism by which Panda restricts nodal expression is unknown. Similarly, what initiates expression of nodal in the ectoderm and what are the mechanisms that link patterning along the primary and secondary axes is not well understood. We report that in Paracentrotus lividus, the activity of the maternally expressed ETS-domain transcription factor Yan/Tel is essential for the spatial restriction of nodal. Inhibiting translation of maternal yan/tel mRNA disrupted dorsal-ventral patterning in all germ layers by causing a massive ectopic expression of nodal starting from cleavage stages, mimicking the phenotype caused by inactivation of the maternal Nodal antagonist Panda. We show that like in the fly or in vertebrates, the activity of sea urchin Yan/Tel is regulated by phosphorylation by MAP kinases. However, unlike in the fly or in vertebrates, phosphorylation by GSK3 plays a central role in the regulation Yan/Tel stability in the sea urchin. We show that GSK3 phosphorylates Yan/Tel in vitro at two different sites including a β-TRCP ubiquitin ligase degradation motif and a C-terminal Ser/Thr rich cluster and that phosphorylation of Yan/Tel by GSK3 triggers its degradation by a β-TRCP/proteasome pathway. Finally, we show that, Yan is epistatic to Panda and that the activity of Yan/Tel is required downstream of Panda to restrict nodal expression. Our results identify Yan/Tel as a central regulator of the spatial expression of nodal in Paracentrotus lividus and uncover a key interaction between the gene regulatory networks responsible for patterning the embryo along the dorsal-ventral and animal-vegetal axes. Public Library of Science 2018-09-17 /pmc/articles/PMC6160229/ /pubmed/30222786 http://dx.doi.org/10.1371/journal.pgen.1007621 Text en © 2018 Molina 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
Molina, M. Dolores
Quirin, Magali
Haillot, Emmanuel
De Crozé, Noémie
Range, Ryan
Rouel, Mathieu
Jimenez, Felipe
Amrouche, Radja
Chessel, Aline
Lepage, Thierry
MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
title MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
title_full MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
title_fullStr MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
title_full_unstemmed MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
title_short MAPK and GSK3/ß-TRCP-mediated degradation of the maternal Ets domain transcriptional repressor Yan/Tel controls the spatial expression of nodal in the sea urchin embryo
title_sort mapk and gsk3/ß-trcp-mediated degradation of the maternal ets domain transcriptional repressor yan/tel controls the spatial expression of nodal in the sea urchin embryo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160229/
https://www.ncbi.nlm.nih.gov/pubmed/30222786
http://dx.doi.org/10.1371/journal.pgen.1007621
work_keys_str_mv AT molinamdolores mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT quirinmagali mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT haillotemmanuel mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT decrozenoemie mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT rangeryan mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT rouelmathieu mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT jimenezfelipe mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT amroucheradja mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT chesselaline mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo
AT lepagethierry mapkandgsk3ßtrcpmediateddegradationofthematernaletsdomaintranscriptionalrepressoryantelcontrolsthespatialexpressionofnodalintheseaurchinembryo