Suppr超能文献

Trim 家族基因与视网膜:表达与功能特征。

The Trim family of genes and the retina: Expression and functional characterization.

机构信息

Department of Genetics, Development and Cell Biology, Iowa State University, Ames, Iowa, United States of America.

出版信息

PLoS One. 2018 Sep 12;13(9):e0202867. doi: 10.1371/journal.pone.0202867. eCollection 2018.

Abstract

To better understand the mechanisms that govern the development of retinal neurons, it is critical to gain additional insight into the specific intrinsic factors that control cell fate decisions and neuronal maturation. In the developing mouse retina, Atoh7, a highly conserved transcription factor, is essential for retinal ganglion cell development. Moreover, Atoh7 expression in the developing retina occurs during a critical time period when progenitor cells are in the process of making cell fate decisions. We performed transcriptome profiling of Atoh7+ individual cells isolated from mouse retina. One of the genes that we found significantly correlated with Atoh7 in our transcriptomic data was the E3 ubiquitin ligase, Trim9. The correlation between Trim9 and Atoh7 coupled with the expression of Trim9 in the early mouse retina led us to hypothesize that this gene may play a role in the process of cell fate determination. To address the role of Trim9 in retinal development, we performed a functional analysis of Trim9 in the mouse and did not detect any morphological changes in the retina in the absence of Trim9. Thus, Trim9 alone does not appear to be involved in cell fate determination or early ganglion cell development in the mouse retina. We further hypothesize that the reason for this lack of phenotype may be compensation by one of the many additional TRIM family members we find expressed in the developing retina.

摘要

为了更好地理解调控视网膜神经元发育的机制,深入了解控制细胞命运决定和神经元成熟的特定内在因素至关重要。在发育中的小鼠视网膜中,高度保守的转录因子 Atoh7 对于神经节细胞的发育是必需的。此外,Atoh7 在发育中的视网膜中的表达发生在祖细胞正在做出细胞命运决定的关键时期。我们对从小鼠视网膜中分离的 Atoh7+单个细胞进行了转录组谱分析。在我们的转录组数据中,与 Atoh7 显著相关的基因之一是 E3 泛素连接酶 Trim9。Trim9 与 Atoh7 的相关性以及 Trim9 在早期小鼠视网膜中的表达使我们假设该基因可能在细胞命运决定过程中发挥作用。为了研究 Trim9 在视网膜发育中的作用,我们在小鼠中进行了 Trim9 的功能分析,并且在没有 Trim9 的情况下,没有检测到视网膜的任何形态变化。因此,Trim9 似乎单独不参与小鼠视网膜中的细胞命运决定或早期神经节细胞发育。我们进一步假设,这种表型缺乏的原因可能是由我们在发育中的视网膜中发现的许多其他 TRIM 家族成员之一代偿所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/566c/6135365/09fe9184ebc0/pone.0202867.g001.jpg

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