A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen

被引:1407
作者
Moffat, J
Grueneberg, DA
Yang, XP
Kim, SY
Kloepfer, AM
Hinkle, G
Piqani, B
Eisenhaure, TM
Luo, B
Grenier, JK
Carpenter, AE
Foo, SY
Stewart, SA
Stockwell, BR
Hacohen, N
Hahn, WC
Lander, ES
Sabatini, DM
Root, DE [1 ]
机构
[1] MIT, Broad Inst, Cambridge, MA 02139 USA
[2] Harvard Univ, Cambridge, MA 02139 USA
[3] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[4] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[5] Dana Farber Canc Inst, Ctr Canc Syst Biol, Boston, MA 02115 USA
[6] MIT, Dept Biol, Cambridge, MA 02139 USA
[7] Massachusetts Gen Hosp, Ctr Immunol & Inflammatory Dis, Boston, MA 02114 USA
[8] Massachusetts Gen Hosp, Div Cardiol, Boston, MA 02114 USA
[9] Harvard Univ, Sch Med, Boston, MA 02115 USA
[10] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63110 USA
[11] Columbia Univ, Dept Chem, Dept Sci Biol, New York, NY 10027 USA
关键词
D O I
10.1016/j.cell.2006.01.040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To enable arrayed or pooled loss-of-function screens in a wide range of mammalian cell types, including primary and nondividing cells, we are developing lentiviral short hairpin RNA (shRNA) libraries targeting the human and murine genomes. The libraries currently contain 104,000 vectors, targeting each of 22,000 human and mouse genes with multiple sequence-verified constructs. To test the utility of the library for arrayed screens, we developed a screen based on high-content imaging to identify genes required for mitotic progression in human cancer cells and applied it to an arrayed set of 5,000 unique shRNA-expressing lentiviruses that target 1,028 human genes. The screen identified several known and similar to 100 candidate regulators of mitotic progression and proliferation; the availability of multiple shRNAs targeting the same gene facilitated functional validation of putative hits. This work provides a widely applicable resource for loss-of-function screens, as well as a roadmap for its application to biological discovery.
引用
收藏
页码:1283 / 1298
页数:16
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