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小鼠 KRAB 锌指蛋白 CHATO 在胚胎衍生组织中控制卵黄囊和胎盘形态发生。

The mouse KRAB zinc-finger protein CHATO is required in embryonic-derived tissues to control yolk sac and placenta morphogenesis.

机构信息

Department of Molecular Biology and Genetics, Cornell University, 259 Biotechnology Building, Ithaca, NY 14853, USA.

出版信息

Dev Biol. 2011 Jan 15;349(2):331-41. doi: 10.1016/j.ydbio.2010.11.015. Epub 2010 Nov 19.

Abstract

Yolk sac and placenta are required to sustain embryonic development in mammals, yet our understanding of the genes and processes that control morphogenesis of these extraembryonic tissues is still limited. The chato mutation disrupts ZFP568, a Krüppel-Associated-Box (KRAB) domain Zinc finger protein, and causes a unique set of extraembryonic malformations, including ruffling of the yolk sac membrane, defective extraembryonic mesoderm morphogenesis and vasculogenesis, failure to close the ectoplacental cavity, and incomplete placental development. Phenotypic analysis of chato embryos indicated that ZFP568 does not control proliferation or differentiation of extraembryonic lineages but rather regulates the morphogenetic events that shape extraembryonic tissues. Analysis of chimeric embryos showed that Zfp568 function is required in embryonic-derived lineages, including the extraembryonic mesoderm. Depleting Zfp568 affects the ability of extraembryonic mesoderm cells to migrate. However, explanted Zfp568 mutant cells could migrate properly when plated on appropriate extracellular matrix conditions. We show that expression of Fibronectin and Indian Hedgehog are reduced in chato mutant yolk sacs. These data suggest that ZFP568 controls the production of secreted factors required to promote morphogenesis of extraembryonic tissues. Our results support previously undescribed roles of the extraembryonic mesoderm in yolk sac morphogenesis and in the closure of the ectoplacental cavity and identify a novel role of ZFP568 in the development of extraembryonic tissues.

摘要

卵黄囊和胎盘是哺乳动物胚胎发育所必需的,但我们对于控制这些胚胎外组织形态发生的基因和过程的理解仍然有限。Chato 突变破坏了 ZFP568,一种 KRAB 结构域锌指蛋白,导致一系列独特的胚胎外畸形,包括卵黄囊膜起皱、胚胎外中胚层形态发生和血管生成缺陷、外胎盘腔闭合失败以及胎盘发育不全。Chato 胚胎的表型分析表明,ZFP568 不控制胚胎外谱系的增殖或分化,而是调节塑造胚胎外组织的形态发生事件。嵌合胚胎的分析表明,Zfp568 功能在胚胎源性谱系中是必需的,包括胚胎外中胚层。耗尽 Zfp568 会影响胚胎外中胚层细胞的迁移能力。然而,当将 Zfp568 突变细胞种植在适当的细胞外基质条件下时,它们可以正常迁移。我们表明,纤维连接蛋白和印度刺猬的表达在 chato 突变的卵黄囊中减少。这些数据表明,ZFP568 控制着产生促进胚胎外组织形态发生的分泌因子的表达。我们的结果支持了胚胎外中胚层在卵黄囊形态发生以及在外胎盘腔闭合中的先前未描述的作用,并确定了 ZFP568 在胚胎外组织发育中的新作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ba/3023455/6a72f604181d/nihms254709f1.jpg

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