Single-cell cDNA microarray profiling of complex biological processes of differentiation

被引:24
作者
Kurimoto, Kazuki [1 ,2 ]
Saitou, Mitinori [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Med, Dept Anat & Cell Biol, Sakyo Ku, Kyoto 6068501, Japan
[2] JST, CREST, Sakyo Ku, Kyoto 6068501, Japan
关键词
PRIMORDIAL GERM-CELLS; EMBRYONIC STEM-CELLS; RNA-SEQ ANALYSIS; GENE-EXPRESSION; MESSENGER-RNA; MOUSE EMBRYO; OLIGONUCLEOTIDE ARRAYS; TRANSCRIPT ANALYSIS; PRIMITIVE ENDODERM; MICE;
D O I
10.1016/j.gde.2010.06.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Gene expression profiling at the single-cell level has been used to identify genes expressed in specific cell populations, in attempts to address various fundamental questions in multicellular organisms. In this article, we review the advance of single-cell cDNA amplification techniques in the last decade, and introduce a recently developed, reliable, quantitative method that is applicable to genome-wide transcriptional analyses with high-density oligonucleotide microarray and massively parallel sequencing. This method has been applied to a variety of biological studies, including developments of blastocyst inner cell mass, neurons, and primordial germ cells, to profile the molecular properties, dynamics during differentiation, and impacts of gene alterations in the individual cells in depth. These studies uncovered complex behaviors of the cells during differentiation in vivo, and identified previously unknown, transient populations that emerged in specific stages of development. These achievements clearly demonstrated that it is now more feasible to analyze gene expression in any cell type of interest in a quantitative, genome-wide manner at the single-cell resolution.
引用
收藏
页码:470 / 477
页数:8
相关论文
共 63 条
[31]  
LAWSON KA, 1991, DEVELOPMENT, V113, P891
[32]   Bmp4 is required for the generation of primordial germ cells in the mouse embryo [J].
Lawson, KA ;
Dunn, NR ;
Roelen, BAJ ;
Zeinstra, LM ;
Davis, AM ;
Wright, CVE ;
Korving, JPWFM ;
Hogan, BLM .
GENES & DEVELOPMENT, 1999, 13 (04) :424-436
[33]   Expression monitoring by hybridization to high-density oligonucleotide arrays [J].
Lockhart, DJ ;
Dong, HL ;
Byrne, MC ;
Follettie, MT ;
Gallo, MV ;
Chee, MS ;
Mittmann, M ;
Wang, CW ;
Kobayashi, M ;
Horton, H ;
Brown, EL .
NATURE BIOTECHNOLOGY, 1996, 14 (13) :1675-1680
[34]   DERIVATION OF PLURIPOTENTIAL EMBRYONIC STEM-CELLS FROM MURINE PRIMORDIAL GERM-CELLS IN CULTURE [J].
MATSUI, Y ;
ZSEBO, K ;
HOGAN, BLM .
CELL, 1992, 70 (05) :841-847
[35]   Microfluidic large-scale integration: The evolution of design rules for biological automation [J].
Melin, Jessica ;
Quake, Stephen R. .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2007, 36 :213-231
[36]   Blimp1 is a critical determinant of the germ cell lineage in mice [J].
Ohinata, Y ;
Payer, B ;
O'Carroll, D ;
Ancelin, K ;
Ono, Y ;
Sano, M ;
Barton, SC ;
Obukhanych, T ;
Nussenzweig, M ;
Tarakhovsky, A ;
Saitou, M ;
Surani, MA .
NATURE, 2005, 436 (7048) :207-213
[37]   A Signaling Principle for the Specification of the Germ Cell Lineage in Mice [J].
Ohinata, Yasuhide ;
Ohta, Hiroshi ;
Shigeta, Mayo ;
Yamanaka, Kaori ;
Wakayama, Teruhiko ;
Saitou, Mitinori .
CELL, 2009, 137 (03) :571-584
[38]   Molecular characterization of melanocyte stem cells in their niche [J].
Osawa, M ;
Egawa, G ;
Mak, SS ;
Moriyama, M ;
Freter, R ;
Yonetani, S ;
Beermann, F ;
Nishikawa, SI .
DEVELOPMENT, 2005, 132 (24) :5589-5599
[39]   Microfluidic digital PCR enables multigene analysis of individual environmental bacteria [J].
Ottesen, Elizabeth A. ;
Hong, Jong Wook ;
Quake, Stephen R. ;
Leadbetter, Jared R. .
SCIENCE, 2006, 314 (5804) :1464-1467
[40]   Distinct sequential cell behaviours direct primitive endoderm formation in the mouse blastocyst [J].
Plusa, Berenika ;
Piliszek, Anna ;
Frankenberg, Stephen ;
Artus, Jerome ;
Hadjantonakis, Anna-Katerina .
DEVELOPMENT, 2008, 135 (18) :3081-3091