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Engrailed-1突变小鼠的多种发育缺陷:早期中后脑缺失以及前肢和胸骨的模式形成缺陷。

Multiple developmental defects in Engrailed-1 mutant mice: an early mid-hindbrain deletion and patterning defects in forelimbs and sternum.

作者信息

Wurst W, Auerbach A B, Joyner A L

机构信息

Division of Molecular and Developmental Biology, Samuel Lunenfeld Research Institute, Mt. Sinai Hospital, Toronto, Canada.

出版信息

Development. 1994 Jul;120(7):2065-75. doi: 10.1242/dev.120.7.2065.

Abstract

During mouse development, the homeobox-containing gene En-1 is specifically expressed across the mid-hindbrain junction, the ventral ectoderm of the limb buds, and in regions of the hindbrain, spinal cord, somites and somite-derived tissues. To address the function of En-1 during embryogenesis, we have generated mice homozygous for a targeted deletion of the En-1 homeobox. En-1 mutant mice died shortly after birth and exhibited multiple developmental defects. In the brains of newborn mutants, most of the colliculi and cerebellum were missing and the third and fourth cranial nerves were absent. A deletion of midhindbrain tissue was observed as early as 9.5 days of embryonic development and the phenotype resembles that previously reported for Wnt-1 mutant mice. In addition, patterning of the forelimb paws and sternum was disrupted, and the 13th ribs were truncated. The results of these studies suggest a cell autonomous role for En-1 in generation and/or survival of mid-hindbrain precursor cells and also a non-cell autonomous role in signalling normal development of the limbs and possibly sternum.

摘要

在小鼠发育过程中,含同源异型框的基因En-1在中脑-后脑交界处、肢芽的腹侧外胚层以及后脑、脊髓、体节和体节衍生组织区域特异性表达。为了研究En-1在胚胎发生过程中的功能,我们构建了En-1同源异型框靶向缺失的纯合小鼠。En-1突变小鼠出生后不久死亡,并表现出多种发育缺陷。在新生突变体的大脑中,大部分丘和小脑缺失,第三和第四对脑神经缺失。早在胚胎发育9.5天时就观察到中后脑组织缺失,其表型与先前报道的Wnt-1突变小鼠相似。此外,前肢爪和胸骨的模式形成受到破坏,第13根肋骨缩短。这些研究结果表明,En-1在中后脑前体细胞的产生和/或存活中具有细胞自主作用,并且在肢体和可能的胸骨正常发育的信号传导中具有非细胞自主作用。

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