Suppr超能文献

小眼症小鼠模型中细胞数量的基因拯救:Chx10与G1期细胞周期调节因子之间的相互作用

Genetic rescue of cell number in a mouse model of microphthalmia: interactions between Chx10 and G1-phase cell cycle regulators.

作者信息

Green Eric S, Stubbs Jennifer L, Levine Edward M

机构信息

Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, UT 84132, USA.

出版信息

Development. 2003 Feb;130(3):539-52. doi: 10.1242/dev.00275.

Abstract

Insufficient cell number is a primary cause of failed retinal development in the Chx10 mutant mouse. To determine if Chx10 regulates cell number by antagonizing p27(Kip1) activity, we generated Chx10, p27(Kip1) double null mice. The severe hypocellular defect in Chx10 single null mice is alleviated in the double null, and while Chx10-null retinas lack lamination, double null retinas have near normal lamination. Bipolar cells are absent in the double null retina, a defect that is attributable to a requirement for Chx10 that is independent of p27(Kip1). We find that p27(Kip1) is abnormally present in progenitors of Chx10-null retinas, and that its ectopic localization is responsible for a significant amount of the proliferation defect in this microphthalmia model system. mRNA and protein expression patterns in these mice and in cyclin D1-null mice suggest that Chx10 influences p27(Kip1) at a post-transcriptional level, through a mechanism that is largely dependent on cyclin D1. This is the first report of rescue of retinal proliferation in a microphthalmia model by deletion of a cell cycle regulatory gene.

摘要

细胞数量不足是Chx10突变小鼠视网膜发育失败的主要原因。为了确定Chx10是否通过拮抗p27(Kip1)活性来调节细胞数量,我们构建了Chx10、p27(Kip1)双缺失小鼠。Chx10单缺失小鼠中严重的细胞减少缺陷在双缺失小鼠中得到缓解,并且虽然Chx10缺失的视网膜缺乏分层,但双缺失的视网膜具有接近正常的分层。双缺失视网膜中没有双极细胞,这种缺陷归因于对Chx10的需求,该需求独立于p27(Kip1)。我们发现p27(Kip1)在Chx10缺失的视网膜祖细胞中异常存在,并且其异位定位是该小眼症模型系统中大量增殖缺陷的原因。这些小鼠和细胞周期蛋白D1缺失小鼠中的mRNA和蛋白质表达模式表明,Chx10在转录后水平上通过一种很大程度上依赖于细胞周期蛋白D1的机制影响p27(Kip1)。这是关于通过缺失细胞周期调节基因来挽救小眼症模型中视网膜增殖的首次报道。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验