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Oligoarray Comparative Genomic Hybridization-Mediated Mapping of Suppressor Mutations Generated in a Deletion-Biased Mutagenesis Screen

机译:Oligoarray比较基因组杂交介导的缺失突变诱变屏幕中产生的抑制子突变的映射。

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摘要

Suppressor screens are an invaluable method for identifying novel genetic interactions between genes in the model organism Caenorhabditis elegans. However, traditionally this approach has suffered from the laborious and protracted process of mapping mutations at the molecular level. Using a mutagen known to generate small deletions, coupled with oligoarray comparative genomic hybridization (aCGH), we have identified mutations in two genes that suppress the lethality associated with a mutation of the essential receptor tyrosine kinase . First, we find that deletion of the Bicaudal-C ortholog, , suppresses –associated lethality. Second, we identify several duplications that also suppress –associated lethality. We establish that overexpression of srap-1, a single gene present in these duplications, mediates the suppression. This study demonstrates the suitability of deletion-biased mutagenesis screening in combination with aCGH characterization for the rapid identification of novel suppressor mutations. In addition to detecting small deletions, this approach is suitable for identifying copy number suppressor mutations, a class of suppressor not easily characterized using alternative approaches.
机译:抑制子筛选是鉴定模型生物秀丽隐杆线虫中基因之间新的遗传相互作用的宝贵方法。然而,传统上,这种方法遭受了在分子水平上定位突变的费力且旷日持久的过程。使用已知会产生小缺失的诱变剂,再加上寡阵列比较基因组杂交(aCGH),我们已经鉴定出两个基因中的突变,这些突变可抑制与必需受体酪氨酸激酶突变相关的致死性。首先,我们发现删除Bicaudal-C直系同源物可以抑制–相关的杀伤力。其次,我们确定了几个重复项,这些重复项也可以抑制相关的杀伤力。我们建立了在这些重复中存在的单个基因srap-1的过表达介导了抑制作用。这项研究表明结合aCGH表征的偏向突变筛选适合快速鉴定新型抑制基因突变。除了检测小的缺失外,该方法还适用于鉴定拷贝数抑制子突变,这是使用替代方法不易表征的一类抑制子。

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