| Literature DB >> 35451459 |
Miho Matsuda1, Chih-Wen Chu1, Sergei Y Sokol1.
Abstract
Apical constriction, or a reduction in size of the apical domain, underlies many morphogenetic events during development. Actomyosin complexes play an essential role in apical constriction; however, the detailed analysis of molecular mechanisms is still pending. Here, we show that Lim domain only protein 7 (Lmo7), a multidomain adaptor at apical junctions, promotes apical constriction in the Xenopus superficial ectoderm, whereas apical domain size increases in Lmo7-depleted cells. Lmo7 is primarily localized at apical junctions and promotes the formation of the dense circumferential actomyosin belt. Strikingly, Lmo7 binds non-muscle myosin II (NMII) and recruits it to apical junctions and the apical cortex. This NMII recruitment is essential for Lmo7-mediated apical constriction. Lmo7 knockdown decreases NMIIA localization at apical junctions and delays neural tube closure in Xenopus embryos. Our findings suggest that Lmo7 serves as a scaffold that regulates actomyosin contractility and apical domain size.Entities:
Keywords: zzm321990 Xenopus ectodermzzm321990 ; Actomyosin contractility; Adherens junctions; Lmo7; Morphogenesis; Non-muscle myosin II
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Year: 2022 PMID: 35451459 PMCID: PMC9188752 DOI: 10.1242/dev.200236
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.862