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针对小鼠14号染色体高度保守的花斑缺失区域进行的必需基因诱变筛选。

An essential gene mutagenesis screen across the highly conserved piebald deletion region of mouse chromosome 14.

作者信息

Hagarman James A, O'Brien Timothy P

机构信息

Department of Biomedical Sciences, Cornell University, Ithaca, New York.

出版信息

Genesis. 2009 Jun;47(6):392-403. doi: 10.1002/dvg.20510.

Abstract

The piebald deletion complex is a set of overlapping chromosomal deficiencies on distal mouse chromosome 14. We surveyed the functional genetic content of the piebald deletion region in an essential gene mutagenesis screen of 952 genomes to recover seven lethal mutants. The ENU-induced mutations were mapped to define genetic intervals using the piebald deletion panel. Lethal mutations included loci required for establishment of the left-right embryonic axis and a loss-of-function allele of Phr1 resulting in respiratory distress at birth. A functional map of the piebald region integrates experimental genetic data from the deletion panel, mutagenesis screen, and the targeted disruption of specific genes. A comparison of several genomic intervals targeted in regional mutagenesis screens suggests that the piebald region is characterized by a low gene density and high essential gene density with a distinct genomic content and organization that supports complex regulatory interactions and promotes evolutionary stability.

摘要

花斑缺失复合体是小鼠14号染色体远端一组重叠的染色体缺失。我们在对952个基因组进行的必需基因诱变筛选中,调查了花斑缺失区域的功能基因内容,以获得7个致死突变体。利用花斑缺失组将ENU诱导的突变进行定位,以确定遗传区间。致死突变包括建立左右胚胎轴所需的基因座,以及Phr1的一个功能丧失等位基因,该等位基因导致出生时呼吸窘迫。花斑区域的功能图谱整合了来自缺失组、诱变筛选以及特定基因靶向破坏的实验遗传数据。对区域诱变筛选中几个靶向基因组区间的比较表明,花斑区域的特点是基因密度低、必需基因密度高,具有独特的基因组内容和组织,支持复杂的调控相互作用并促进进化稳定性。

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