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Epigenetic marks in cloned rhesus monkey embryos: Comparison with counterparts produced in vitro
Yang JF4,5; Yang SH4; Beaujean N6,7; Niu YY4; He XC4; Xie YH4; Tang XH4; Wang L7; Zhou Q*7; Ji WZ*4; qzhou@ioz.ac.cn; wji@mail.kiz.ac.cn
2007
发表期刊BIOLOGY OF REPRODUCTION
ISSN0006-3363
卷号76期号:1页码:36-42
合作性质其它
摘要Until now, no primate animals have been successfully cloned to birth with somatic cell nuclear transfer (SCNT) procedures, and little is known about the molecular events that occurred in the reconstructed embryos during preimplantation development. In many SCNT cases, epigenetic reprogramming of the donor nuclei after transfer into enucleated oocytes was hypothesized to be crucial to the reestablishment of embryonic totipotency. In the present study, we focused on two major epigenetic marks, DNA methylation and histone H3 lysine 9 (H3K9) acetylation, which we examined by indirect immunofluorescence and confocal laser scanning microscopy. During preimplantation development, 67% of two-cell- and 50% of eight-cell-cloned embryos showed higher DNA methylation levels than their in vitro fertilization (IVF) counterparts, which undergo gradual demethylation until the early morula stage. Moreover, whereas an asymmetric distribution of DNA methylation was established in an IVF blastocysts with a lower methylation level in the inner cell mass (ICM) than in the trophectoderm, in most cloned blastocysts, ICM cells maintained a high degree of methylation. Finally, two donor cell lines (S11 and S1-04) that showed a higher level of H3K9 acetylation supported more blastocyst formation after nuclear transfer than the other cell line (S1-03), with a relatively low level of acetylation staining. In conclusion, we propose that abnormal DNA methylation patterns contribute to the poor quality of cloned preimplantation embryos and may be one of the obstacles to successful cloning in primates.
关键词Dna Methylation Donor Cells Early Development Embryo
资助者Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois). ; Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois). ; Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois). ; Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois).
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收录类别SCI
语种英语
资助者Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois). ; Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois). ; Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois). ; Supported by Major Projects of Knowledge Innovation Program from the Chinese Academy of Sciences (KSCX1-05), National Natural Science Foundation of China (30370166), Joint Scholar Plan for the Development of Western China, National Basic Research Program of China (973 program, 2004CCA01300), and the PRA (Programme de Recherches Avance´es Franco—Chinois).
文献类型期刊论文
条目标识符http://ir.kiz.ac.cn/handle/152453/5619
专题生殖与发育生物学
科研部门_哺乳动物胚胎发育(郑萍)
中国科学院昆明灵长类研究中心
通讯作者qzhou@ioz.ac.cn; wji@mail.kiz.ac.cn
作者单位1.**
2.**
3.***
4.Department of Reproduction and Development,Kunming Institute of Zoology & Kunming Primate Research Center, the Chinese Academy of Sciences, Kunming, Yunnan 650223, China
5.Graduate University of Chinese Academy of Sciences,Beijing 100049, China
6.INRA,UMR 1198; ENVA; CNRS, FRE 2857, Biologie du De ´veloppement et Reproduction, Jouy en Josas, F-78350, France
7.The State Key Laboratory of Reproductive Biology,Institute of Zoology, the Chinese Academy of Sciences, Beijing 100860, China
推荐引用方式
GB/T 7714
Yang JF,Yang SH,Beaujean N,et al. Epigenetic marks in cloned rhesus monkey embryos: Comparison with counterparts produced in vitro[J]. BIOLOGY OF REPRODUCTION,2007,76(1):36-42.
APA Yang JF.,Yang SH.,Beaujean N.,Niu YY.,He XC.,...&wji@mail.kiz.ac.cn.(2007).Epigenetic marks in cloned rhesus monkey embryos: Comparison with counterparts produced in vitro.BIOLOGY OF REPRODUCTION,76(1),36-42.
MLA Yang JF,et al."Epigenetic marks in cloned rhesus monkey embryos: Comparison with counterparts produced in vitro".BIOLOGY OF REPRODUCTION 76.1(2007):36-42.
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