Axolotl Nanog activity in mouse embryonic stem cells demonstrates that ground state pluripotency is conserved from urodele amphibians to mammals

被引:46
作者
Dixon, James E. [1 ]
Allegrucci, Cinzia [1 ,2 ]
Redwood, Catherine [1 ]
Kump, Kevin [3 ]
Bian, Yuhong [1 ]
Chatfield, Jodie [1 ]
Chen, Yi-Hsien [1 ]
Sottile, Virginie [4 ]
Voss, S. Randal [3 ]
Alberio, Ramiro [1 ]
Johnson, Andrew D. [1 ]
机构
[1] Univ Nottingham, Queens Med Ctr, Inst Genet, Sch Biol, Nottingham NG2 2UH, England
[2] Univ Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, Leics, England
[3] Univ Kentucky, Dept Biol, Lexington, KY 40506 USA
[4] Univ Nottingham, Wolfson Ctr Stem Cells Tissue Engn & Modelling, Nottingham NG7 2RD, England
来源
DEVELOPMENT | 2010年 / 137卷 / 18期
基金
英国医学研究理事会;
关键词
Pluripotency; Nanog; Axolotl; Xenopus; GERM-CELLS; SELF-RENEWAL; EXPRESSION; SPECIFICATION; EPIBLAST; REPRESSION; EVOLUTION; NETWORK; LINES; SALL4;
D O I
10.1242/dev.049262
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cells in the pluripotent ground state can give rise to somatic cells and germ cells, and the acquisition of pluripotency is dependent on the expression of Nanog. Pluripotency is conserved in the primitive ectoderm of embryos from mammals and urodele amphibians, and here we report the isolation of a Nanog ortholog from axolotls (axNanog). axNanog does not contain a tryptophan repeat domain and is expressed as a monomer in the axolotl animal cap. The monomeric form is sufficient to regulate pluripotency in mouse embryonic stem cells, but axNanog dimers are required to rescue LIF-independent self-renewal. Our results show that protein interactions mediated by Nanog dimerization promote proliferation. More importantly, they demonstrate that the mechanisms governing pluripotency are conserved from urodele amphibians to mammals.
引用
收藏
页码:2973 / 2980
页数:8
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