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骨形态发生蛋白-4是小鼠中胚层形成和模式化所必需的。

Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse.

作者信息

Winnier G, Blessing M, Labosky P A, Hogan B L

机构信息

Howard Hughes Medical Institute, Vanderbilt University Medical School, Nashville, Tennessee 37232-2175, USA.

出版信息

Genes Dev. 1995 Sep 1;9(17):2105-16. doi: 10.1101/gad.9.17.2105.

Abstract

Bone morphogenetic protein-4 (BMP-4) is a member of the TGF-beta superfamily of polypeptide signaling molecules, closely related to BMP-2 and to Drosophila decapentaplegic (DPP). To elucidate the role of BMP-4 in mouse development the gene has been inactivated by homologous recombination in ES cells. Homozygous mutant Bmp-4tm1blh embryos die between 6.5 and 9.5 days p.c., with a variable phenotype. Most Bmp-4tm1blh embryos do not proceed beyond the egg cylinder stage, do not express the mesodermal marker T(Brachyury), and show little or no mesodermal differentiation. Some homozygous mutants develop to the head fold or beating heart/early somite stage or beyond. However, they are developmentally retarded and have truncated or disorganized posterior structures and a reduction in extraembryonic mesoderm, including blood islands. These results provide direct genetic evidence that BMP-4 is essential for several different processes in early mouse development, beginning with gastrulation and mesoderm formation. Moreover, in the presumed absence of zygotic ligand, it appears that homozygous mutants can be rescued partially by related proteins or by maternal BMP-4.

摘要

骨形态发生蛋白-4(BMP-4)是多肽信号分子TGF-β超家族的成员,与BMP-2和果蝇的decapentaplegic(DPP)密切相关。为了阐明BMP-4在小鼠发育中的作用,该基因已通过胚胎干细胞中的同源重组而失活。纯合突变体Bmp-4tm1blh胚胎在妊娠6.5至9.5天之间死亡,表现出可变的表型。大多数Bmp-4tm1blh胚胎不会超过卵圆柱期,不表达中胚层标记T(Brachyury),并且几乎没有或没有中胚层分化。一些纯合突变体发育到头部折叠或跳动心脏/早期体节阶段或更后期。然而,它们发育迟缓,后部结构截断或紊乱,包括血岛在内的胚外中胚层减少。这些结果提供了直接的遗传学证据,表明BMP-4对于小鼠早期发育中的几个不同过程至关重要,从原肠胚形成和中胚层形成开始。此外,在假定没有合子配体的情况下,纯合突变体似乎可以被相关蛋白或母体BMP-4部分挽救。

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