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RhoGAP RGA-8 通过使上皮细胞极化来支持 形态发生。

RhoGAP RGA-8 supports morphogenesis in by polarizing epithelia.

机构信息

Department of Pathology and Laboratory Medicine, Rutgers - RWJMS, Piscataway, NJ 08854, USA.

Cell and Developmental Biology Graduate Program, School of Graduate Studies, Rutgers - RWJMS, Piscataway, NJ 08854, USA.

出版信息

Biol Open. 2020 Nov 26;9(11):bio056911. doi: 10.1242/bio.056911.

DOI:10.1242/bio.056911
PMID:33243762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7710025/
Abstract

CDC-42 regulation of non-muscle myosin/NMY-2 is required for polarity maintenance in the one-cell embryo of CDC-42 and NMY-2 regulate polarity throughout embryogenesis, but their contribution to later events of morphogenesis are less understood. We have shown that epidermal enclosure requires the GTPase CED-10/Rac1 and WAVE/Scar complex, its effector, to promote protrusions that drive enclosure through the branch actin regulator Arp2/3. Our analysis here of RGA-8, a homolog of SH3BP1/Rich1/ARHGAP17/Nadrin, with BAR and RhoGAP motifs, suggests it regulates CDC-42, so that actin and myosin/NMY-2 promote ventral enclosure during embryonic morphogenesis. Genetic and molecular data suggest RGA-8 regulates CDC-42, and phenocopies the CDC-42 pathway regulators WASP-1/WSP-1 and the F-BAR proteins TOCA-1 and TOCA-2. Live imaging shows RGA-8 and WSP-1 enrich myosin and regulate F-actin in migrating epidermal cells during ventral enclosure. Loss of RGA-8 alters membrane recruitment of active CDC-42. We propose TOCA proteins and RGA-8 use BAR domains to localize and regenerate CDC-42 activity, thus regulating F-actin levels, through the branched actin regulator WSP-1, and myosin enrichment. RhoGAP RGA-8 thus polarizes epithelia, to promote cell migrations and cell shape changes of embryonic morphogenesis.

摘要

CDC-42 对非肌肉肌球蛋白/NMY-2 的调节对于单细胞胚胎的极性维持是必需的 CDC-42 和 NMY-2 在整个胚胎发生过程中调节极性,但它们对形态发生后期事件的贡献了解较少。我们已经表明,表皮封闭需要 GTPase CED-10/Rac1 和 WAVE/Scar 复合物及其效应物,以促进突起,通过分支肌动蛋白调节剂 Arp2/3 驱动封闭。我们在这里对 RGA-8 的分析,SH3BP1/Rich1/ARHGAP17/Nadrin 的同源物,具有 BAR 和 RhoGAP 基序,表明它调节 CDC-42,因此肌动蛋白和肌球蛋白/NMY-2 促进胚胎形态发生期间的腹侧封闭。遗传和分子数据表明 RGA-8 调节 CDC-42,并模拟了 CDC-42 途径调节剂 WASP-1/WSP-1 和 F-BAR 蛋白 TOCA-1 和 TOCA-2。实时成像显示 RGA-8 和 WSP-1 在腹侧封闭期间富集肌球蛋白并调节迁移表皮细胞中的 F-肌动蛋白。RGA-8 的缺失改变了活性 CDC-42 的膜募集。我们提出 TOCA 蛋白和 RGA-8 使用 BAR 结构域来定位和再生 CDC-42 活性,从而通过分支肌动蛋白调节剂 WSP-1 和肌球蛋白富集来调节 F-肌动蛋白水平。RhoGAP RGA-8 因此使上皮细胞极化,以促进胚胎形态发生的细胞迁移和细胞形状变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/12fbf83523f7/biolopen-9-056911-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/78c0d2f04eef/biolopen-9-056911-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/6cd28f3712be/biolopen-9-056911-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/54a984d163fa/biolopen-9-056911-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/42ebf29b064e/biolopen-9-056911-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/31b2b59426a7/biolopen-9-056911-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/12fbf83523f7/biolopen-9-056911-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/78c0d2f04eef/biolopen-9-056911-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/6cd28f3712be/biolopen-9-056911-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/54a984d163fa/biolopen-9-056911-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/42ebf29b064e/biolopen-9-056911-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/31b2b59426a7/biolopen-9-056911-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e410/7710025/12fbf83523f7/biolopen-9-056911-g6.jpg

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