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Birth of parthenogenetic mice that can develop to adulthood

DC FieldValueLanguage
dc.contributor.author박은성-
dc.date.accessioned2015-07-14T17:29:08Z-
dc.date.available2015-07-14T17:29:08Z-
dc.date.issued2004-
dc.identifier.issn0028-0836-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/112977-
dc.description.abstractOnly mammals have relinquished parthenogenesis, a means of producing descendants solely from maternal germ cells. Mouse parthenogenetic embryos die by day 10 of gestation. Bi-parental reproduction is necessary because of parent-specific epigenetic modification of the genome during gametogenesis. This leads to unequal expression of imprinted genes from the maternal and paternal alleles. However, there is no direct evidence that genomic imprinting is the only barrier to parthenogenetic development. Here we show the development of a viable parthenogenetic mouse individual from a reconstructed oocyte containing two haploid sets of maternal genome, derived from non-growing and fully grown oocytes. This development was made possible by the appropriate expression of the Igf2 and H19 genes with other imprinted genes, using mutant mice with a 13-kilobase deletion in the H19 gene as non-growing oocytes donors. This full-term development is associated with a marked reduction in aberrantly expressed genes. The parthenote developed to adulthood with the ability to reproduce offspring. These results suggest that paternal imprinting prevents parthenogenesis, ensuring that the paternal contribution is obligatory for the descendant.-
dc.description.statementOfResponsibilityopen-
dc.format.extent860~864-
dc.relation.isPartOfNATURE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHEmbryonic and Fetal Development/genetics-
dc.subject.MESHEpigenesis, Genetic-
dc.subject.MESHFemale-
dc.subject.MESHGene Expression Profiling-
dc.subject.MESHGene Expression Regulation, Developmental-
dc.subject.MESHGenomic Imprinting/genetics-
dc.subject.MESHHaploidy-
dc.subject.MESHInsulin-Like Growth Factor II/genetics-
dc.subject.MESHMale-
dc.subject.MESHMice/embryology*-
dc.subject.MESHMice/genetics-
dc.subject.MESHMice/growth & development*-
dc.subject.MESHMutation-
dc.subject.MESHOligonucleotide Array Sequence Analysis-
dc.subject.MESHOocytes/cytology-
dc.subject.MESHOocytes/metabolism-
dc.subject.MESHParthenogenesis/genetics-
dc.subject.MESHParthenogenesis/physiology*-
dc.subject.MESHRNA, Long Noncoding-
dc.subject.MESHRNA, Messenger/genetics-
dc.subject.MESHRNA, Messenger/metabolism-
dc.subject.MESHRNA, Untranslated/genetics-
dc.titleBirth of parthenogenetic mice that can develop to adulthood-
dc.typeArticle-
dc.contributor.collegeResearcher Institutes (부설 연구소)-
dc.contributor.departmentInstitute for Medical Convergence (연의-생공연 메디컬융합연구소)-
dc.contributor.googleauthorTomohiro Kono-
dc.contributor.googleauthorYayoi Obata-
dc.contributor.googleauthorHidehiko Ogawa-
dc.contributor.googleauthorJeong-Sun Seo-
dc.contributor.googleauthorEun Sung Park-
dc.contributor.googleauthorYuji Yamamoto-
dc.contributor.googleauthorYukiko Ono-
dc.contributor.googleauthorKatsutoshi Niwa-
dc.contributor.googleauthorQuiong Wu-
dc.identifier.doi10.1038/nature02402-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01609-
dc.relation.journalcodeJ02289-
dc.identifier.eissn1476-4687-
dc.identifier.pmid15103378-
dc.contributor.alternativeNamePark, Eun Sung-
dc.contributor.affiliatedAuthorPark, Eun Sung-
dc.rights.accessRightsfree-
dc.citation.volume428-
dc.citation.number6985-
dc.citation.startPage860-
dc.citation.endPage864-
dc.identifier.bibliographicCitationNATURE, Vol.428(6985) : 860-864, 2004-
Appears in Collections:
5. Research Institutes (연구소) > Institute for Medical Convergence (연의-생공연 메디컬융합연구소) > 1. Journal Papers

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