Nucleologenesis and embryonic genome activation are defective in interspecies cloned embryos between bovine ooplasm and rhesus monkey somatic cells

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dc.contributor.authorBong Seok Song-
dc.contributor.authorS H Lee-
dc.contributor.authorSun-Uk Kim-
dc.contributor.authorJi Su Kim-
dc.contributor.authorJung Sun Park-
dc.contributor.authorC H Kim-
dc.contributor.authorKyu Tae Chang-
dc.contributor.authorY M Han-
dc.contributor.authorK K Lee-
dc.contributor.authorD S Lee-
dc.contributor.authorDeog Bon Koo-
dc.date.accessioned2017-04-19T09:14:23Z-
dc.date.available2017-04-19T09:14:23Z-
dc.date.issued2009-
dc.identifier.issn1471-213X-
dc.identifier.uri10.1186/1471-213X-9-44ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/9078-
dc.description.abstractBackground. Interspecies somatic cell nuclear transfer (iSCNT) has been proposed as a tool to address basic developmental questions and to improve the feasibility of cell therapy. However, the low efficiency of iSCNT embryonic development is a crucial problem when compared to in vitro fertilization (IVF) and intraspecies SCNT. Thus, we examined the effect of donor cell species on the early development of SCNT embryos after reconstruction with bovine ooplasm. Results. No apparent difference in cleavage rate was found among IVF, monkey-bovine (MB)-iSCNT, and bovine-bovine (BB)-SCNT embryos. However, MB-iSCNT embryos failed to develop beyond the 8- or 16-cell stages and lacked expression of the genes involved in embryonic genome activation (EGA) at the 8-cell stage. From ultrastructural observations made during the peri-EGA period using transmission electron microscopy (TEM), we found that the nucleoli of MB-iSCNT embryos were morphologically abnormal or arrested at the primary stage of nucleologenesis. Consistent with the TEM analysis, nucleolar component proteins, such as upstream binding transcription factor, fibrillarin, nucleolin, and nucleophosmin, showed decreased expression and were structurally disorganized in MB-iSCNT embryos compared to IVF and BB-SCNT embryos, as revealed by real-time PCR and immunofluorescence confocal laser scanning microscopy, respectively. Conclusion. The down-regulation of housekeeping and imprinting genes, abnormal nucleolar morphology, and aberrant patterns of nucleolar proteins during EGA resulted in developmental failure in MB-iSCNT embryos. These results provide insight into the unresolved problems of early embryonic development in iSCNT embryos. ⓒ 2009 Song et al; licensee BioMed Central Ltd.-
dc.publisherSpringer-BMC-
dc.titleNucleologenesis and embryonic genome activation are defective in interspecies cloned embryos between bovine ooplasm and rhesus monkey somatic cells-
dc.title.alternativeNucleologenesis and embryonic genome activation are defective in interspecies cloned embryos between bovine ooplasm and rhesus monkey somatic cells-
dc.typeArticle-
dc.citation.titleBMC Developmental Biology-
dc.citation.number0-
dc.citation.endPage44-
dc.citation.startPage44-
dc.citation.volume9-
dc.contributor.affiliatedAuthorBong Seok Song-
dc.contributor.affiliatedAuthorSun-Uk Kim-
dc.contributor.affiliatedAuthorJi Su Kim-
dc.contributor.affiliatedAuthorJung Sun Park-
dc.contributor.affiliatedAuthorKyu Tae Chang-
dc.contributor.affiliatedAuthorDeog Bon Koo-
dc.contributor.alternativeName송봉석-
dc.contributor.alternativeName이상희-
dc.contributor.alternativeName김선욱-
dc.contributor.alternativeName김지수-
dc.contributor.alternativeName박정선-
dc.contributor.alternativeName김철희-
dc.contributor.alternativeName장규태-
dc.contributor.alternativeName한용만-
dc.contributor.alternativeName이경광-
dc.contributor.alternativeName이동석-
dc.contributor.alternativeName구덕본-
dc.identifier.bibliographicCitationBMC Developmental Biology, vol. 9, pp. 44-44-
dc.identifier.doi10.1186/1471-213X-9-44-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
Jeonbuk Branch Institute > Primate Resources Center > 1. Journal Articles
Aging Convergence Research Center > 1. Journal Articles
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