Pluripotential competence of cells associated with Nanog activity

被引:198
作者
Hatano, S
Tada, M
Kimura, H
Yamaguchi, S
Kono, T
Nakano, T
Suemori, H
Nakatsuji, N
Tada, T
机构
[1] Kyoto Univ, Inst Frontier Med Sci, Sakyo Ku, Kyoto 6068507, Japan
[2] ReproCELL Inc, Chiyoda Ku, Tokyo 1000011, Japan
[3] Tokyo Univ Agr, Dept Biosci, Setagaya Ku, Tokyo 1568502, Japan
[4] Osaka Univ, Sch Med, Suita, Osaka 5650871, Japan
[5] Osaka Univ, Grad Sch Frontier Biosci, Suita, Osaka 5650871, Japan
关键词
Nanog; ES cell; pluripotency; reprogramming; targeting; cell fusion; clone; human; monkey; mouse;
D O I
10.1016/j.mod.2004.08.008
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nanog is a novel pluripotential cell-specific gene that plays a crucial role in maintaining the undifferentiated state of early, postimplantation embryos and embryonic stem (ES) cells. We have explored the expression pattern and function of Nanog and a Nanog-homologue. Nanog-ps1.Nanog-ps1 was mapped on Chromosome 7 and shown to be a pseudogene. Immunocytochemical analysis in vivo Showed that the NANOG protein was absent in unfertilized oocytes, and was detected in cells of morula-stage embryos, the inner cell mass of blastocysts and the epiblast of E6.5 and E7.5 embryos, but not in primordial germ cells of early postimplantation embryos. In monkey and human ES cells. NANOG expression was restricted to undifferentiated cells. Furthermore, reactivation of the somatic cell-derived Nanog was tightly linked with nuclear reprogramming induced by cell hybridization with ES cells and by nuclear transplantation into enucleated oocyte. Notably. mouse Nanog (+/-) ES cells. which produced approximately half the amount of NANOG produced by wild-type ES cells. readily differentiated to multi-lineage cells in culture medium including LIF. The labile undifferentiated state was fully rescued by constitutive expression of exogenous Nanog. Thus, the activity of Nanog is tightly correlated with an undifferentiated state of cells even in nuclear reprogrammed somatic cells. Nanog may function as a key regulator for sustaining pluripotency in a dose-dependent manner. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:67 / 79
页数:13
相关论文
共 39 条
[1]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[2]   Multipotent cell lineages in early mouse development depend on SOX2 function [J].
Avilion, AA ;
Nicolis, SK ;
Pevny, LH ;
Perez, L ;
Vivian, N ;
Lovell-Badge, R .
GENES & DEVELOPMENT, 2003, 17 (01) :126-140
[3]   Oct4 distribution and level in mouse clones:: consequences for pluripotency [J].
Boiani, M ;
Eckardt, S ;
Schöler, HR ;
McLaughlin, KJ .
GENES & DEVELOPMENT, 2002, 16 (10) :1209-1219
[4]   Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells [J].
Chambers, I ;
Colby, D ;
Robertson, M ;
Nichols, J ;
Lee, S ;
Tweedie, S ;
Smith, A .
CELL, 2003, 113 (05) :643-655
[5]   Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal polycomb sites [J].
Czermin, B ;
Melfi, R ;
McCabe, D ;
Seitz, V ;
Imhof, A ;
Pirrotta, V .
CELL, 2002, 111 (02) :185-196
[6]   BIOLOGICAL VARIATION IN GLYCATED PROTEINS [J].
DAVIE, SJ ;
WHITING, KL ;
GOULD, BJ .
ANNALS OF CLINICAL BIOCHEMISTRY, 1993, 30 :260-264
[7]   X-chromosomes inactivation in cloned mouse embryos [J].
Eggan, K ;
Akutsu, H ;
Hochedlinger, K ;
Rideout, W ;
Yanagimachi, R ;
Jaenisch, R .
SCIENCE, 2000, 290 (5496) :1578-1581
[8]   Consequences of the depletion of zygotic and embryonic enhancer of zeste 2 during preimplantation mouse development [J].
Erhardt, S ;
Su, IH ;
Schneider, R ;
Barton, S ;
Bannister, AJ ;
Perez-Burgos, L ;
Jenuwein, T ;
Kouzarides, T ;
Tarakhovsky, A ;
Surani, MA .
DEVELOPMENT, 2003, 130 (18) :4235-4248
[9]   Identification, cloning and expression analysis of the pluripotency promoting Nanog genes in mouse and human [J].
Hart, AH ;
Hartley, L ;
Ibrahim, M ;
Robb, L .
DEVELOPMENTAL DYNAMICS, 2004, 230 (01) :187-198
[10]   Histone code modifications on pluripotential nuclei of reprogrammed somatic cells [J].
Kimura, H ;
Tada, M ;
Nakatsuji, N ;
Tada, T .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (13) :5710-5720