4.7 Article

Direct activation of Shroom3 transcription by Pitx proteins drives epithelial morphogenesis in the developing gut

期刊

DEVELOPMENT
卷 137, 期 8, 页码 1339-1349

出版社

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.044610

关键词

Pitx1; Pitx2; Shroom; Apical constriction; Epithelium; Gut; Xenopus

资金

  1. NSF [IOB 0642012]
  2. Canadian Institutes of Health Research [MOP-74663]
  3. NIH/NIGMS
  4. March of Dimes
  5. Burroughs Wellcome Fund
  6. Howard Hughes Medical Institute

向作者/读者索取更多资源

Individual cell shape changes are essential for epithelial morphogenesis. A transcriptional network for epithelial cell shape change is emerging in Drosophila, but this area remains largely unexplored in vertebrates. The distinction is important as so far, key downstream effectors of cell shape change in Drosophila appear not to be conserved. Rather, Shroom3 has emerged as a central effector of epithelial morphogenesis in vertebrates, driving both actin-and microtubule-based cell shape changes. To date, the morphogenetic role of Shroom3 has been explored only in the neural epithelium, so the broad expression of this gene raises two important questions: what are the requirements for Shroom3 in non-neural tissues and what factors control Shroom3 transcription? Here, we show in Xenopus that Shroom3 is essential for cell shape changes and morphogenesis in the developing vertebrate gut and that Shroom3 transcription in the gut requires the Pitx1 transcription factor. Moreover, we show that Pitx proteins directly activate Shroom3 transcription, and we identify Pitx-responsive regulatory elements in the genomic DNA upstream of Shroom3. Finally, we show that ectopic expression of Pitx proteins is sufficient to induce Shroom3-dependent cytoskeletal reorganization and epithelial cell shape change. These data demonstrate new breadth to the requirements for Shroom3 in morphogenesis, and they also provide a cell-biological basis for the role of Pitx transcription factors in morphogenesis. More generally, these results provide a foundation for deciphering the transcriptional network that underlies epithelial cell shape change in developing vertebrates.

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