A whole genome RNAi screen of Drosophila S2 cell spreading performed using automated computational image analysis

被引:25
作者
D'Ambrosio, Michael V. [1 ,2 ]
Vale, Ronald D. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
关键词
DYNAMICS; PROTEIN; LAMELLA;
D O I
10.1083/jcb.201003135
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent technological advances in microscopy have enabled cell-based whole genome screens, but the analysis of the vast amount of image data generated by such screens usually proves to be rate limiting In this study, we performed a whole genome RNA interference (RNAi) screen to uncover genes that affect spreading of Drosophila melanogaster S2 cells using several computational methods for analyzing the image data in an automated manner Expected genes in the Scar Arp2/3 actin nucleation pathway were identified as well as casein kinase I, which had a similar morphological RNAi signature A distinct nonspreading morphological phenotype was identified for genes involved in membrane secretion or synthesis In this group, we identified a new secretory peptide and investigated the functions of two poorly characterized endoplasmic reticulum proteins that have roles in secretion Thus, this genome wide screen succeeded in identifying known and unexpected proteins that are important for cell spreading, and the computational tools developed in this study should prove useful for other types of automated whole genome screens
引用
收藏
页码:471 / 478
页数:8
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