Genomewide gain-of-function genetic screen identifies functionally active genes in mouse embryonic stem cells

被引:75
作者
Pritsker, M [1 ]
Ford, NR [1 ]
Jenq, HT [1 ]
Lemischkat, LR [1 ]
机构
[1] Princeton Univ, Dept Biol Mol, Princeton, NJ 08544 USA
关键词
cDNA library; differentiation; microarray; phenotype; self-renewal;
D O I
10.1073/pnas.0509861103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Embryonic stem (ES) cells hold great promise for the future of medicine. To elucidate the molecular mechanisms that control ES cell self-renewal and differentiation, a comprehensive knowledge of the molecules involved in these processes is required. Here we describe an effective approach for genomewide identification of functionally active genes in ES cells. This approach combines genetic screens based on cDNA libraries with microarray detection methods to permit high-throughput functional analyses. We implement this strategy to identify genes whose overexpression can maintain phenotypic properties of undifferentiated mouse ES cells under differentiation-inducing conditions, specifically in the absence of leukemia inhibitory factor. The identified genes encode a variety of regulatory proteins whose function in ES cells was previously unknown. Moreover, our approach is capable of detecting genes whose overexpression promote differentiation or cell death. Overall, our studies establish a methodology for highly sensitive identification of genes that confer particular phenotypes on ES cells.
引用
收藏
页码:6946 / 6951
页数:6
相关论文
共 44 条
[1]   Identification of Zfp-57 as a downstream molecule of STAT3 and Oct-3/4 in embryonic stem cells [J].
Akagi, T ;
Usuda, M ;
Matsuda, T ;
Ko, MSH ;
Niwa, H ;
Asano, M ;
Koide, H ;
Yokota, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 331 (01) :23-30
[2]   The Src family of tyrosine kinases is important for embryonic stem cell self-renewal [J].
Annerén, C ;
Cowan, CA ;
Melton, DA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (30) :31590-31598
[3]   Selection analyses of insertional mutants using subgenic-resolution arrays [J].
Badarinarayana, V ;
Estep, PW ;
Shendure, J ;
Edwards, J ;
Tavazoie, S ;
Lam, F ;
Church, GM .
NATURE BIOTECHNOLOGY, 2001, 19 (11) :1060-1065
[4]   Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator [J].
Bamforth, SD ;
Bragança, J ;
Eloranta, JJ ;
Murdoch, JN ;
Marques, FIR ;
Kranc, KR ;
Farza, H ;
Henderson, DJ ;
Hurst, HC ;
Bhattacharya, S .
NATURE GENETICS, 2001, 29 (04) :469-474
[5]   Spi-C, a novel Ets protein that is temporally regulated during B lymphocyte development [J].
Bemark, M ;
Mårtensson, A ;
Liberg, D ;
Leanderson, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :10259-10267
[6]   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
[7]   Regulatory networks in embryo-derived pluripotent stem cells [J].
Boiani, M ;
Schöler, HR .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (11) :872-884
[8]   Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei [J].
Bortvin, A ;
Eggan, K ;
Skaletsky, H ;
Akutsu, H ;
Berry, DL ;
Yanagimachi, R ;
Page, DC ;
Jaenisch, R .
DEVELOPMENT, 2003, 130 (08) :1673-1680
[9]   Core transcriptional regulatory circuitry in human embryonic stem cells [J].
Boyer, LA ;
Lee, TI ;
Cole, MF ;
Johnstone, SE ;
Levine, SS ;
Zucker, JR ;
Guenther, MG ;
Kumar, RM ;
Murray, HL ;
Jenner, RG ;
Gifford, DK ;
Melton, DA ;
Jaenisch, R ;
Young, RA .
CELL, 2005, 122 (06) :947-956
[10]   LIF/STAT3 controls ES cell self-renewal and pluripotency by a Myc-dependent mechanism [J].
Cartwright, P ;
McLean, C ;
Sheppard, A ;
Rivett, D ;
Jones, K ;
Dalton, S .
DEVELOPMENT, 2005, 132 (05) :885-896