Cargando…
Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration
Pitx2c, a homeodomain transcription factor, is classically known for its left-right patterning role. However, an early wave of pitx2 expression occurs at the onset of gastrulation in several species, indicating a possible earlier role that remains relatively unexplored. Here we show that in zebrafis...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023614/ https://www.ncbi.nlm.nih.gov/pubmed/29952749 http://dx.doi.org/10.7554/eLife.34880 |
_version_ | 1783335903796658176 |
---|---|
author | Collins, Michelle M Maischein, Hans-Martin Dufourcq, Pascale Charpentier, Marine Blader, Patrick Stainier, Didier YR |
author_facet | Collins, Michelle M Maischein, Hans-Martin Dufourcq, Pascale Charpentier, Marine Blader, Patrick Stainier, Didier YR |
author_sort | Collins, Michelle M |
collection | PubMed |
description | Pitx2c, a homeodomain transcription factor, is classically known for its left-right patterning role. However, an early wave of pitx2 expression occurs at the onset of gastrulation in several species, indicating a possible earlier role that remains relatively unexplored. Here we show that in zebrafish, maternal-zygotic (MZ) pitx2c mutants exhibit a shortened body axis indicative of convergence and extension (CE) defects. Live imaging reveals that MZpitx2c mutants display less persistent mesendodermal migration during late stages of gastrulation. Transplant data indicate that Pitx2c functions cell non-autonomously to regulate this cell behavior by modulating cell shape and protrusive activity. Using transcriptomic analyses and candidate gene approaches, we identify transcriptional changes in components of the chemokine-ECM-integrin dependent mesendodermal migration network. Together, our results define pathways downstream of Pitx2c that are required during early embryogenesis and reveal novel functions for Pitx2c as a regulator of morphogenesis. |
format | Online Article Text |
id | pubmed-6023614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-60236142018-07-05 Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration Collins, Michelle M Maischein, Hans-Martin Dufourcq, Pascale Charpentier, Marine Blader, Patrick Stainier, Didier YR eLife Developmental Biology Pitx2c, a homeodomain transcription factor, is classically known for its left-right patterning role. However, an early wave of pitx2 expression occurs at the onset of gastrulation in several species, indicating a possible earlier role that remains relatively unexplored. Here we show that in zebrafish, maternal-zygotic (MZ) pitx2c mutants exhibit a shortened body axis indicative of convergence and extension (CE) defects. Live imaging reveals that MZpitx2c mutants display less persistent mesendodermal migration during late stages of gastrulation. Transplant data indicate that Pitx2c functions cell non-autonomously to regulate this cell behavior by modulating cell shape and protrusive activity. Using transcriptomic analyses and candidate gene approaches, we identify transcriptional changes in components of the chemokine-ECM-integrin dependent mesendodermal migration network. Together, our results define pathways downstream of Pitx2c that are required during early embryogenesis and reveal novel functions for Pitx2c as a regulator of morphogenesis. eLife Sciences Publications, Ltd 2018-06-28 /pmc/articles/PMC6023614/ /pubmed/29952749 http://dx.doi.org/10.7554/eLife.34880 Text en © 2018, Collins et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Collins, Michelle M Maischein, Hans-Martin Dufourcq, Pascale Charpentier, Marine Blader, Patrick Stainier, Didier YR Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
title | Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
title_full | Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
title_fullStr | Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
title_full_unstemmed | Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
title_short | Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
title_sort | pitx2c orchestrates embryonic axis extension via mesendodermal cell migration |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023614/ https://www.ncbi.nlm.nih.gov/pubmed/29952749 http://dx.doi.org/10.7554/eLife.34880 |
work_keys_str_mv | AT collinsmichellem pitx2corchestratesembryonicaxisextensionviamesendodermalcellmigration AT maischeinhansmartin pitx2corchestratesembryonicaxisextensionviamesendodermalcellmigration AT dufourcqpascale pitx2corchestratesembryonicaxisextensionviamesendodermalcellmigration AT charpentiermarine pitx2corchestratesembryonicaxisextensionviamesendodermalcellmigration AT bladerpatrick pitx2corchestratesembryonicaxisextensionviamesendodermalcellmigration AT stainierdidieryr pitx2corchestratesembryonicaxisextensionviamesendodermalcellmigration |