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PlexinA1 与 PTK7 相互作用,是神经嵴迁移所必需的。

PlexinA1 interacts with PTK7 and is required for neural crest migration.

机构信息

Department of Developmental Biochemistry, Center for Molecular Physiology of the Brain (CMPB), GZMB, University of Göttingen, Justus-von-Liebig-Weg 11, 37077 Göttingen, Germany.

出版信息

Biochem Biophys Res Commun. 2010 Nov 12;402(2):402-7. doi: 10.1016/j.bbrc.2010.10.044. Epub 2010 Oct 12.

Abstract

Members of the plexin protein family are known regulators of axon guidance, but recent data indicate that they have broader functions in the regulation of embryonic morphogenesis. Here we provide further evidence of this by showing that PlexinA1 is expressed in Xenopus neural crest cells and is required for their migration. PlexinA1 expression is detected in migrating cranial neural crest cells and knockdown of PlexinA1 expression using Morpholino oligonucleotides inhibits neural crest migration. PlexinA1 likely affects neural crest migration by interaction with PTK7, a regulator of planar cell polarity that is required for neural crest migration. PlexinA1 and PTK7 interact in immunoprecipitation assays and show phenotypic interaction in co-injection experiments. Considering that plexins and PTK7 have been shown to genetically interact in Drosophila axon guidance and chick cardiac morphogenesis, our data suggest that this interaction is evolutionary conserved and may be relevant for a broad range of morphogenetic events including the migration of neural crest cells in Xenopus laevis.

摘要

聚蛋白家族成员是已知的轴突导向调节剂,但最近的数据表明它们在胚胎形态发生的调节中具有更广泛的功能。在这里,我们通过显示 PlexinA1 在非洲爪蟾神经嵴细胞中表达并需要其迁移来提供进一步的证据。在迁移的颅神经嵴细胞中检测到 PlexinA1 表达,并且使用 Morpholino 寡核苷酸敲低 PlexinA1 表达抑制神经嵴迁移。PlexinA1 可能通过与 PTK7 的相互作用影响神经嵴迁移,PTK7 是平面细胞极性的调节剂,是神经嵴迁移所必需的。PlexinA1 和 PTK7 在免疫沉淀测定中相互作用,并在共注射实验中表现出表型相互作用。考虑到聚蛋白和 PTK7 已在果蝇轴突导向和鸡心脏形态发生中显示出遗传相互作用,我们的数据表明这种相互作用是进化保守的,可能与包括非洲爪蟾神经嵴细胞迁移在内的广泛形态发生事件有关。

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