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突变型Vg1配体破坏非洲爪蟾胚胎中内胚层和中胚层的形成。

Mutant Vg1 ligands disrupt endoderm and mesoderm formation in Xenopus embryos.

作者信息

Joseph E M, Melton D A

机构信息

Howard Hughes Medical Institute, Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

Development. 1998 Jul;125(14):2677-85. doi: 10.1242/dev.125.14.2677.

Abstract

The Xenopus Vg1 gene, a TGFbeta superfamily member, is expressed as a maternal mRNA localized to prospective endoderm, and mature Vg1 protein can induce both endodermal and mesodermal markers in embryonic cells. Most previous work on embryonic inducers, including activin, BMPs and Vg1, has relied on ectopic expression to assay for gene function. Here we employ a mutant ligand approach to block Vg1 signaling in developing embryos. The results indicate that Vg1 expression is essential for normal endodermal development and the induction of dorsal mesoderm in vivo.

摘要

非洲爪蟾Vg1基因是转化生长因子β(TGFβ)超家族成员,作为一种定位于预期内胚层的母源mRNA表达,成熟的Vg1蛋白可在胚胎细胞中诱导内胚层和中胚层标志物的表达。此前关于胚胎诱导因子(包括激活素、骨形态发生蛋白(BMPs)和Vg1)的大多数研究都依赖于异位表达来分析基因功能。在此,我们采用突变配体方法来阻断发育中胚胎的Vg1信号传导。结果表明,Vg1表达对于体内正常的内胚层发育和背侧中胚层的诱导至关重要。

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