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在内脏内胚层中表达的肝细胞核因子4(HNF-4)基因的破坏,会导致胚胎外胚层细胞死亡,并损害小鼠胚胎的原肠胚形成。

Disruption of the HNF-4 gene, expressed in visceral endoderm, leads to cell death in embryonic ectoderm and impaired gastrulation of mouse embryos.

作者信息

Chen W S, Manova K, Weinstein D C, Duncan S A, Plump A S, Prezioso V R, Bachvarova R F, Darnell J E

机构信息

Laboratory of Molecular Cell Biology, Rockefeller University, New York, New York 10021.

出版信息

Genes Dev. 1994 Oct 15;8(20):2466-77. doi: 10.1101/gad.8.20.2466.

Abstract

Expression of HNF-4, a transcription factor in the steroid hormone receptor superfamily, is detected only in the visceral endoderm of mouse embryos during gastrulation and is expressed in certain embryonic tissues from 8.5 days of gestation. To examine the role of HNF-4 during embryonic development, we disrupted the gene in embryonic stem cells and found that the homozygous loss of functional HNF-4 protein was an embryonic lethal. Cell death was evident in the embryonic ectoderm at 6.5 days when these cells normally initiate gastrulation. As assessed by expression of Brachyury and HNF-3 beta, primitive streak formation and initial differentiation of mesoderm do occur, but with a delay of approximately 24 h. Development of embryonic structures is severely impaired. These results demonstrate that the expression of HNF-4 in the visceral endoderm is essential for embryonic ectoderm survival and normal gastrulation.

摘要

肝细胞核因子4(HNF-4)是类固醇激素受体超家族中的一种转录因子,仅在小鼠胚胎原肠胚形成期的脏内胚层中被检测到,并且从妊娠8.5天开始在某些胚胎组织中表达。为了研究HNF-4在胚胎发育过程中的作用,我们在胚胎干细胞中破坏了该基因,发现功能性HNF-4蛋白的纯合缺失是胚胎致死性的。在6.5天时,当这些细胞正常开始原肠胚形成时,胚胎外胚层中明显出现细胞死亡。通过短尾型基因(Brachyury)和肝细胞核因子3β(HNF-3 beta)的表达评估,中胚层的原条形成和初始分化确实会发生,但会延迟约24小时。胚胎结构的发育严重受损。这些结果表明,脏内胚层中HNF-4的表达对于胚胎外胚层的存活和正常原肠胚形成至关重要。

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