Hekimi S, Boutis P, Lakowski B
Department of Biology, McGill University, Montréal, Québec, Canada.
Genetics. 1995 Dec;141(4):1351-64. doi: 10.1093/genetics/141.4.1351.
We carried out a genetic screen for viable maternal-effect mutants to identify genes with a critical function relatively early in development. This type of mutation would not have been identified readily in previous screens for viable mutants and therefore could define previously unidentified genes. We screened 30,000 genomes and identified 41 mutations falling into 24 complementation groups. We genetically mapped these 24 loci; only two of them appear to correspond to previously identified genes. We present a partial phenotypic characterization of the mutants and a quantitative analysis of the degree to which they can be maternally or zygotically rescued.
我们开展了一项针对可行的母体效应突变体的基因筛选,以鉴定在发育相对早期具有关键功能的基因。这种类型的突变在之前针对可行突变体的筛选中不容易被识别,因此可能会定义先前未鉴定的基因。我们筛选了30000个基因组,鉴定出41个突变,这些突变分为24个互补群。我们对这24个位点进行了遗传定位;其中只有两个似乎对应于先前鉴定的基因。我们展示了这些突变体的部分表型特征,以及对它们可以在母体或合子水平上被挽救的程度的定量分析。