Specific gene-regulation networks during the pre-implantation development of the pig embryo as revealed by deep sequencing.
Specific gene-regulation networks during the pre-implantation development of the pig embryo as revealed by deep sequencing.
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DOI:
10.1186/1471-2164-15-4
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发表时间:
2014-01-03
期刊:
影响因子:
4.4
通讯作者:
Li N
中科院分区:
文献类型:
--
作者:
Cao S;Han J;Wu J;Li Q;Liu S;Zhang W;Pei Y;Ruan X;Liu Z;Wang X;Lim B;Li N
Because few studies exist to describe the unique molecular network regulation behind pig pre-implantation embryonic development (PED), genetic engineering in the pig embryo is limited. Also, this lack of research has hindered derivation and application of porcine embryonic stem cells and porcine induced pluripotent stem cells (iPSCs). We identified and analyzed the genome wide transcriptomes of pig in vivo-derived and somatic cell nuclear transferred (SCNT) as well as mouse in vivo-derived pre-implantation embryos at different stages using mRNA deep sequencing. Comparison of the pig embryonic transcriptomes with those of mouse and human pre-implantation embryos revealed unique gene expression patterns during pig PED. Pig zygotic genome activation was confirmed to occur at the 4-cell stage via genome-wide gene expression analysis. This activation was delayed to the 8-cell stage in SCNT embryos. Specific gene expression analysis of the putative inner cell mass (ICM) and the trophectoderm (TE) revealed that pig and mouse pre-implantation embryos share regulatory networks during the first lineage segregation and primitive endoderm differentiation, but not during ectoderm commitment. Also, fatty acid metabolism appears to be a unique characteristic of pig pre-implantation embryonic development. In addition, the global gene expression patterns in the pig SCNT embryos were different from those in in vivo-derived pig embryos. Our results provide a resource for pluripotent stem cell engineering and for understanding pig development. The online version of this article (doi:10.1186/1471-2164-15-4) contains supplementary material, which is available to authorized users.
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影响因子:
1.8
作者:
Lorthongpanich, Chanchao;Laowtammathron, Chuti;Parnpai, Rangsun
通讯作者:
Parnpai, Rangsun
DOI:
10.1089/clo.2009.0004
发表时间:
2009-06-01
期刊:
CLONING AND STEM CELLS
影响因子:
--
作者:
Chung, Young;Bishop, Colin E.;Lanza, Robert
通讯作者:
Lanza, Robert
影响因子:
2.5
作者:
Hall, Vanessa J.;Christensen, Josef;Hyttel, Poul
通讯作者:
Hyttel, Poul
影响因子:
64.8
作者:
BRAUDE, P;BOLTON, V;MOORE, S
通讯作者:
MOORE, S
影响因子:
4.8
作者:
Esteban, Miguel A.;Xu, Jianyong;Pei, Duanqing
通讯作者:
Pei, Duanqing