Pitx2c orchestrates embryonic axis extension via mesendodermal cell migration

被引:9
作者
Collins, Michelle M. [1 ]
Maischein, Hans-Martin [1 ]
Dufourcq, Pascale [2 ]
Charpentier, Marine [3 ]
Blader, Patrick [2 ]
Stainier, Didier Y. R. [1 ]
机构
[1] Max Planck Inst Heart & Lung Res, Dept Dev Genet, Bad Nauheim, Germany
[2] Univ Toulouse III Paul Sabatier, CNRS, Ctr Biol Integrat, Ctr Biol Dev, Toulouse, France
[3] CNRS, INSERM, U1154, Museum Natl Hist Nat, Paris, France
来源
ELIFE | 2018年 / 7卷
关键词
LEFT-RIGHT ASYMMETRY; AXENFELD-RIEGER SYNDROME; GASTRULATION MOVEMENTS; CONVERGENT EXTENSION; SIGNALING CONTROLS; EXTRACELLULAR-MATRIX; DORSAL MIGRATION; HOMEOBOX GENE; ZEBRAFISH; POLARITY;
D O I
10.7554/eLife.34880
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 MZ pitx2c 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. DOI: https://doi.org/10.7554/eLife.34880.001
引用
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页数:24
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