Pooled RNAi Screens - Technical and Biological Aspects

被引:14
作者
Boettcher, M. [1 ]
Hoheisel, J. D. [1 ]
机构
[1] Deutsch Krebsforschungszentrum, Div Funct Genome Anal, D-69120 Heidelberg, Germany
关键词
Pooled RNAi screen; molecular tag; barcode; shRNA library; microarray; half hairpin; SACCHAROMYCES-CEREVISIAE GENOME; HUMAN-CELLS; MAMMALIAN-CELLS; SHRNA LIBRARIES; FUNCTIONAL-ANALYSIS; CANCER GENETICS; ESSENTIAL GENES; INTERFERENCE; PATHWAY; MOUSE;
D O I
10.2174/138920210791110988
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
RNA interference (RNAi) screens have recently emerged as an exciting new tool for studying gene function in mammalian cells. In order to facilitate those studies, short hairpin RNA (shRNA) expression libraries covering the entire human transcriptome have become commercially available. To make use of the full potential of such large-scale shRNA libraries, microarray-based methods have been developed to analyze complex pooled RNAi screens. In terms of microarray analysis, different strategies have been pursued by different research groups, largely influenced by the employed shRNA library. In this review, we compare the three major shRNA expression libraries with a focus on their suitability for a microarray-based analysis of pooled screens. We analyze and compare approaches previously used to perform pooled RNAi screens and point out their advantages as well as limitations.
引用
收藏
页码:162 / 167
页数:6
相关论文
共 37 条
[1]   Lentiviral-mediated RNA interference [J].
Abbas-Terki, T ;
Blanco-Bose, W ;
Déglon, N ;
Pralong, W ;
Aebischer, P .
HUMAN GENE THERAPY, 2002, 13 (18) :2197-2201
[2]   Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes [J].
Ashrafi, K ;
Chang, FY ;
Watts, JL ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Ruvkun, G .
NATURE, 2003, 421 (6920) :268-272
[3]  
Bassik MC, 2009, NAT METHODS, V6, P443, DOI [10.1038/NMETH.1330, 10.1038/nmeth.1330]
[4]   shRNA libraries and their use in cancer genetics [J].
Bernards, Rene ;
Brummelkamp, Thijn R. ;
Beijersbergen, Roderick L. .
NATURE METHODS, 2006, 3 (09) :701-706
[5]   A large-scale RNAi screen in human cells identifies new components of the p53 pathway [J].
Berns, K ;
Hijmans, EM ;
Mullenders, J ;
Brummelkamp, TR ;
Velds, A ;
Heimerikx, M ;
Kerkhoven, RM ;
Madiredjo, M ;
Nijkamp, W ;
Weigelt, B ;
Agami, R ;
Ge, W ;
Cavet, G ;
Linsley, PS ;
Beijersbergen, RL ;
Bernards, R .
NATURE, 2004, 428 (6981) :431-437
[6]   A functional genetic approach identifies the PI3K pathway as a major determinant of trastuzumab resistance in breast cancer [J].
Berns, Katrien ;
Horlings, Hugo M. ;
Hennessy, Bryan T. ;
Madiredjo, Mandy ;
Hijmans, E. Marielle ;
Beelen, Karin ;
Linn, Sabine C. ;
Gonzalez-Angulo, Ana Maria ;
Stemke-Hale, Katherine ;
Hauptmann, Michael ;
Beijersbergen, Roderick L. ;
Mills, Gordon B. ;
de Vijver, Marc J. van ;
Bernards, Rene .
CANCER CELL, 2007, 12 (04) :395-402
[7]   Genome-wide survey of protein kinases required for cell cycle progression [J].
Bettencourt-Dias, M ;
Giet, R ;
Sinka, R ;
Mazumdar, A ;
Lock, WG ;
Balloux, F ;
Zafiropoulos, PJ ;
Yamaguchi, S ;
Winter, S ;
Carthew, RW ;
Cooper, M ;
Jones, D ;
Frenz, L ;
Glover, DM .
NATURE, 2004, 432 (7020) :980-987
[8]   Decoding pooled RNAi screens by means of barcode tiling arrays [J].
Boettcher, Michael ;
Fredebohm, Johannes ;
Gholami, Amin Moghaddas ;
Hachmo, Yafit ;
Dotan, Iris ;
Canaani, Dan ;
Hoheisel, Joerg D. .
BMC GENOMICS, 2010, 11
[9]   Kinase requirements in human cells: III. Altered kinase requirements in VHL-/- cancer cells detected in a pilot synthetic lethal screen [J].
Bommi-Reddy, Archana ;
Almeciga, Ingrid ;
Sawyer, Jacqueline ;
Geisen, Christoph ;
Li, Wenliang ;
Harlow, Ed ;
Kaelin, William G., Jr. ;
Grueneberg, Dorre A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (43) :16484-16489
[10]   Genome-wide RNAi analysis of growth and viability in Drosophila cells [J].
Boutros, M ;
Kiger, AA ;
Armknecht, S ;
Kerr, K ;
Hild, M ;
Koch, B ;
Haas, SA ;
Paro, R ;
Perrimon, N .
SCIENCE, 2004, 303 (5659) :832-835