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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...

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Autores principales: Collins, Michelle M, Maischein, Hans-Martin, Dufourcq, Pascale, Charpentier, Marine, Blader, Patrick, Stainier, Didier YR
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
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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.
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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
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