Conservation of methylation reprogramming in mammalian development: Aberrant reprogramming in cloned embryos

被引:762
作者
Dean, W
Santos, F
Stojkovic, M
Zakhartchenko, V
Walter, J
Wolf, E
Reik, W [1 ]
机构
[1] Babraham Inst, Dev Genet Program, Lab Dev Genet & Imprinting, Cambridge CB2 4AT, England
[2] Univ Munich, Gene Ctr, Inst Mol Anim Breeding, D-81377 Munich, Germany
[3] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[4] Univ Saarland, D-66041 Saarbrucken, Germany
关键词
D O I
10.1073/pnas.241522698
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
Mouse embryos undergo genome-wide methylation reprogramming by demethylation in early preimplantation development, followed by remethylation thereafter. Here we show that genome-wide reprogramming is conserved in several mammalian species and ask whether it also occurs in embryos cloned with the use of highly methylated somatic donor nuclei. Normal bovine, rat, and pig zygotes showed a demethylated paternal genome, suggesting active demethylation. In bovine embryos methylation was further reduced during cleavage up to the eight-cell stage, and this reduction in methylation was followed by de novo methylation by the 16-cell stage. in cloned one-cell embryos there was a reduction in methylation consistent with active demethylation, but no further demethylation occurred subsequently. Instead, de novo methylation and nuclear reorganization of methylation patterns resembling those of differentiated cells occurred precociously in many cloned embryos. Cloned, but not normal, morulae had highly methylated nuclei in all blastomeres that resembled those of the fibroblast donor cells. Our study shows that epigenetic reprogramming occurs aberrantly in most cloned embryos; incomplete reprogramming may contribute to the low efficiency of cloning.
引用
收藏
页码:13734 / 13738
页数:5
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