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转录因子基因AP-2γ对小鼠早期发育至关重要。

Transcription factor gene AP-2 gamma essential for early murine development.

作者信息

Werling Uwe, Schorle Hubert

机构信息

Forschungszentrum Karlsruhe, ITG, Institute for Toxicology and Genetics, 76344 Eggenstein-Leopoldshafen, Germany.

出版信息

Mol Cell Biol. 2002 May;22(9):3149-56. doi: 10.1128/MCB.22.9.3149-3156.2002.

Abstract

Transcription factor gene AP-2 gamma belongs to a family of four closely related genes. AP-2 gamma had been implicated in multiple functions during proliferation and differentiation based on its expression pattern in trophoblast, neural crest, and ectoderm cells in murine embryos. In order to address the question of the role of AP-2 gamma during mammalian development, we generated mice harboring a disrupted AP-2 gamma allele. AP-2 gamma heterozygous mice are viable and display reduced body sizes at birth but are fertile. Mice deficient for AP-2 gamma, however, are growth retarded and die at days 7 to 9 of embryonic development. Immunohistochemical analysis revealed that the trophectodermal cells that are found to express AP-2 gamma fail to proliferate, leading to failure of labyrinth layer formation. As a consequence, the developing embryo suffers from malnutrition and dies. Analysis of embryo cultures suggests that AP-2 gamma is also implicated in the regulation of the adenosine deaminase (ADA) gene, a gene involved in purine metabolism found expressed at the maternal-fetal interface. Therefore, AP-2 gamma seems to be required in early embryonic development because it regulates the genetic programs controlling proliferation and differentiation of extraembryonic trophectodermal cells.

摘要

转录因子基因AP - 2γ属于一个由四个密切相关基因组成的家族。基于其在小鼠胚胎的滋养层、神经嵴和外胚层细胞中的表达模式,AP - 2γ在增殖和分化过程中涉及多种功能。为了解决AP - 2γ在哺乳动物发育中的作用问题,我们培育了携带AP - 2γ等位基因破坏的小鼠。AP - 2γ杂合小鼠是可存活的,出生时体型减小,但可育。然而,AP - 2γ缺陷的小鼠生长迟缓,并在胚胎发育的第7至9天死亡。免疫组织化学分析显示,被发现表达AP - 2γ的滋养外胚层细胞无法增殖,导致迷路层形成失败。结果,发育中的胚胎营养不良并死亡。胚胎培养分析表明,AP - 2γ也参与腺苷脱氨酶(ADA)基因的调控,ADA基因参与嘌呤代谢,在母胎界面表达。因此,AP - 2γ似乎在早期胚胎发育中是必需的,因为它调节控制胚外滋养外胚层细胞增殖和分化的遗传程序。

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