Suppr超能文献

[ENU 突变小鼠的特征分析。使用形态学和分子方法建立人类疾病动物模型]

[Characterization of ENU-mutant mice. Animal models for human diseases using morphological and molecular methods].

作者信息

Wagner S, Calzada-Wack J, Rosemann M, Becker L, Tost M, Silva-Buttkus P, Klein-Rodewald T, Fuchs H, Neff F, Hrabé de Angelis M, Esposito I

机构信息

Institut für Experimentelle Genetik, München.

出版信息

Pathologe. 2010 Oct;31 Suppl 2:147-52. doi: 10.1007/s00292-010-1347-5.

Abstract

Following sequencing of the human genome there are new challenges to decipher the knowledge concerning gene function and the role of gene interactions and pathways leading to disease. Mouse models have proven to be an ideal tool for this purpose. Point mutations induced by chemical mutagenesis by N-ethyl-N-nitrosourea (ENU) offer possibilities for the analysis of the phenotypic outcome of a single base pair exchange on the entire organism. The Munich ENU mouse mutagenesis project is part of the worldwide efforts to obtain mutations for each gene. The generation of new alleles or allelic series offers relevant insights into the relevance of single gene sections. Various mouse models for human diseases have been generated by a systematic large-scale genome-wide phenotyping screen in the last decade. This work illustrates how the implementation of the ENU mouse mutagenesis project with gene identification and parallel high-throughput screening is taking advantage of local cooperation with experienced phenotyping groups at the Helmholtz Zentrum München, leading to major advances in the functional analysis of the mammalian genome.

摘要

人类基因组测序完成后,在解读有关基因功能、基因相互作用的作用以及导致疾病的途径等知识方面出现了新的挑战。事实证明,小鼠模型是实现这一目的的理想工具。通过N-乙基-N-亚硝基脲(ENU)化学诱变诱导的点突变为分析单个碱基对交换在整个生物体上的表型结果提供了可能。慕尼黑ENU小鼠诱变项目是全球为每个基因获取突变所做努力的一部分。新等位基因或等位基因系列的产生为深入了解单个基因片段的相关性提供了相关见解。在过去十年中,通过系统的大规模全基因组表型筛选,已经产生了各种人类疾病的小鼠模型。这项工作说明了实施带有基因鉴定和并行高通量筛选的ENU小鼠诱变项目是如何利用与慕尼黑亥姆霍兹中心经验丰富的表型分析团队的本地合作,从而在哺乳动物基因组功能分析方面取得重大进展的。

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