Schlabach Michael R, Luo Ji, Solimini Nicole L, Hu Guang, Xu Qikai, Li Mamie Z, Zhao Zhenming, Smogorzewska Agata, Sowa Mathew E, Ang Xiaolu L, Westbrook Thomas F, Liang Anthony C, Chang Kenneth, Hackett Jennifer A, Harper J Wade, Hannon Gregory J, Elledge Stephen J
Howard Hughes Medical Institute and Department of Genetics, Center for Genetics and Genomics, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Science. 2008 Feb 1;319(5863):620-4. doi: 10.1126/science.1149200.
Retroviral short hairpin RNA (shRNA)-mediated genetic screens in mammalian cells are powerful tools for discovering loss-of-function phenotypes. We describe a highly parallel multiplex methodology for screening large pools of shRNAs using half-hairpin barcodes for microarray deconvolution. We carried out dropout screens for shRNAs that affect cell proliferation and viability in cancer cells and normal cells. We identified many shRNAs to be antiproliferative that target core cellular processes, such as the cell cycle and protein translation, in all cells examined. Moreover, we identified genes that are selectively required for proliferation and survival in different cell lines. Our platform enables rapid and cost-effective genome-wide screens to identify cancer proliferation and survival genes for target discovery. Such efforts are complementary to the Cancer Genome Atlas and provide an alternative functional view of cancer cells.
逆转录病毒短发夹RNA(shRNA)介导的哺乳动物细胞基因筛选是发现功能缺失表型的强大工具。我们描述了一种高度并行的多重方法,用于使用半发夹条形码进行微阵列解卷积来筛选大量shRNA文库。我们对影响癌细胞和正常细胞增殖及活力的shRNA进行了缺失筛选。我们鉴定出许多靶向核心细胞过程(如细胞周期和蛋白质翻译)的抗增殖shRNA,这些过程在所有检测的细胞中都存在。此外,我们还鉴定出了不同细胞系增殖和存活所选择性必需的基因。我们的平台能够进行快速且经济高效的全基因组筛选,以鉴定用于靶点发现的癌症增殖和存活基因。这些努力与癌症基因组图谱相辅相成,并提供了癌细胞的另一种功能视角。