Piano Fabio, Schetter Aaron J, Morton Diane G, Gunsalus Kristin C, Reinke Valerie, Kim Stuart K, Kemphues Kenneth J
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Curr Biol. 2002 Nov 19;12(22):1959-64. doi: 10.1016/s0960-9822(02)01301-5.
Recently, a set of 766 genes that are enriched in the ovary as compared to the soma was identified by microarray analysis [1]. Here, we report a functional analysis of 98% of these genes by RNA interference (RNAi). Over half the genes tested showed at least one detectable phenotype, most commonly embryonic lethality, consistent with the expectation that ovary transcripts would be enriched for genes that are essential in basic cellular and developmental processes. We find that essential genes are more likely to be conserved and to be highly expressed in the ovary. We extend previous observations and find that fewer than the expected number of ovary-expressed essential genes are present on the X chromosome. We characterized early embryonic defects for 161 genes and used time-lapse microscopy to systematically describe the defects for each gene in terms of 47 RNAi-associated phenotypes. In this paper, we discuss the use of these data to group genes into "phenoclusters"; in the accompanying paper, we use these data as one component in the integration of different types of large-scale functional analyses. We find that phenoclusters correlate well with sequence-based functional predictions and thus may be useful in predicting functions of uncharacterized genes.
最近,通过微阵列分析鉴定出一组与体细胞相比在卵巢中富集的766个基因[1]。在此,我们报告了通过RNA干扰(RNAi)对这些基因中98%进行的功能分析。超过一半的测试基因显示出至少一种可检测到的表型,最常见的是胚胎致死性,这与卵巢转录本会富集在基本细胞和发育过程中必不可少的基因这一预期一致。我们发现必需基因更有可能是保守的,并且在卵巢中高表达。我们扩展了先前的观察结果,发现X染色体上存在的卵巢表达必需基因数量少于预期。我们对161个基因的早期胚胎缺陷进行了表征,并使用延时显微镜根据47种与RNAi相关的表型系统地描述了每个基因的缺陷。在本文中,我们讨论了利用这些数据将基因分组为“表型簇”;在随附的论文中,我们将这些数据用作整合不同类型大规模功能分析的一个组成部分。我们发现表型簇与基于序列的功能预测相关性良好,因此可能有助于预测未表征基因的功能。