Microarrays of lentiviruses for gene function screens in immortalized and primary cells

被引:112
作者
Bailey, SN
Ali, SM
Carpenter, AE
Higgins, CO
Sabatini, DM
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] Broad Inst, Cambridge, MA 02141 USA
关键词
D O I
10.1038/NMETH848
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we describe lentivirus-infected cell microarrays for the high-throughput screening of gene function in mammalian cells. To create these arrays, we cultured mammalian cells on glass slides 'printed' with lentiviruses pseudotyped as vesicular stomatitis virus glycoprotein, which encode short hairpin RNA or cDNA. Cells that land on the printed 'features' become infected with lentivirus, creating a living array of stably transduced cell clusters within a monolayer of uninfected cells. The small size of the features of the microarrays (300 pm in diameter) allows high-density spotting of lentivirus, permitting thousands of distinct parallel infections on a single glass slide. Because lentiviruses have a wide cellular tropism, including primary cells, lentivirus-infected cell microarrays can be used as a platform for high-throughput screening in a variety of cell types.
引用
收藏
页码:117 / 122
页数:6
相关论文
共 14 条
[1]   Innovation - New tools for functional mammalian cancer genetics [J].
Brummelkamp, TR ;
Bernards, R .
NATURE REVIEWS CANCER, 2003, 3 (10) :781-789
[2]  
FEDERICO M, 2003, LENTIVIRAL GENE ENG
[3]   An expanding role for mTOR in cancer [J].
Guertin, DA ;
Sabatini, DM .
TRENDS IN MOLECULAR MEDICINE, 2005, 11 (08) :353-361
[4]   Polyplexes and lipoplexes for mammalian gene delivery:: From traditional to microarray screening [J].
How, SE ;
Yingyongnarongkul, B ;
Fara, MA ;
Diaz-Mochón, JJ ;
Mittoo, S ;
Bradley, M .
COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2004, 7 (05) :423-430
[5]   GENERATION OF LARGE NUMBERS OF DENDRITIC CELLS FROM MOUSE BONE-MARROW CULTURES SUPPLEMENTED WITH GRANULOCYTE MACROPHAGE COLONY-STIMULATING FACTOR [J].
INABA, K ;
INABA, M ;
ROMANI, N ;
AYA, H ;
DEGUCHI, M ;
IKEHARA, S ;
MURAMATSU, S ;
STEINMAN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1693-1702
[6]   RNAi microarray analysis in cultured mammalian cells [J].
Mousses, S ;
Caplen, NJ ;
Cornelison, R ;
Weaver, D ;
Basik, M ;
Hautaniemi, S ;
Elkahloun, AG ;
Lotufo, RA ;
Choudary, A ;
Dougherty, ER ;
Suh, E ;
Kallioniemi, O .
GENOME RESEARCH, 2003, 13 (10) :2341-2347
[7]   In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector [J].
Naldini, L ;
Blomer, U ;
Gallay, P ;
Ory, D ;
Mulligan, R ;
Gage, FH ;
Verma, IM ;
Trono, D .
SCIENCE, 1996, 272 (5259) :263-267
[8]   A lentivirus-based system to functionally silence genes in primary mammalian cells, stem cells and transgenic mice by RNA interference [J].
Rubinson, DA ;
Dillon, CP ;
Kwiatkowski, AV ;
Sievers, C ;
Yang, LL ;
Kopinja, J ;
Zhang, MD ;
McManus, MT ;
Gertler, FB ;
Scott, ML ;
Van Parijs, L .
NATURE GENETICS, 2003, 33 (03) :401-406
[9]   Rictor, a novel binding partner of mTOR, defines a rapamycin-insensitive and raptor-independent pathway that regulates the cytoskeleton [J].
Sarbassov, DD ;
Ali, SM ;
Kim, DH ;
Guertin, DA ;
Latek, RR ;
Erdjument-Bromage, H ;
Tempst, P ;
Sabatini, DM .
CURRENT BIOLOGY, 2004, 14 (14) :1296-1302
[10]   RNA interference microarrays: High-throughput loss-of-function genetics in mammalian cells [J].
Silva, JM ;
Mizuno, H ;
Brady, A ;
Lucito, R ;
Hannon, GJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (17) :6548-6552