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  DNA methylation in the IGF2 intragenic DMR is re-established in a sex-specific manner in bovine blastocysts after somatic cloning.

Geberta, C., Wrenzyckia, C., Herrmann, D., Gröger, D., Thiel, J., Reinhardt, R., et al. (2009). DNA methylation in the IGF2 intragenic DMR is re-established in a sex-specific manner in bovine blastocysts after somatic cloning. Genomics, 94(1), 63-69. Retrieved from http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WG1-4VYP93F-1&_user=28761&_coverDate=07%2F31%2F2009&_rdoc=1&_fmt=high&_orig=search&_sort=d&_docanchor=&view=c&_acct=C000002718&_version=1&_urlVersion=0&_userid=28761&md5=66994da7b0000fca304cfe9cd5576a1c.

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Genre: Journal Article
Alternative Title : Genomics

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 Creators:
Geberta, Claudia, Author
Wrenzyckia, Christine, Author
Herrmann, Doris, Author
Gröger, Daniela1, Author
Thiel, Janina1, Author
Reinhardt, Richard2, Author           
Lehrach, Hans3, Author           
Hajkova, Petra, Author
Lucas-Hahn, Andrea, Author
Carnwath, Joseph W., Author
Niemann, Heiner, Author
Affiliations:
1Max Planck Society, ou_persistent13              
2High Throughput Technologies, Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433552              
3Dept. of Vertebrate Genomics (Head: Hans Lehrach), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433550              

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Free keywords: Genomic imprinting; Somatic cloning; Bovine embryos; Sex-specific DNA methylation; Epigenetic reprogramming
 Abstract: The recent identification of an intragenic differentially methylated region (DMR) within the last exon of the bovine Insulin-like growth factor 2 (IGF2) gene provides a diagnostic tool for in-depth investigation of bovine imprinting and regulatory mechanisms which are active during embryo development. Here, we used bisulfite sequencing to compare sex-specific DNA methylation patterns within this DMR in bovine blastocysts produced in vivo, by in vitro fertilization and culture, SCNT, androgenesis or parthenogenesis. In in vivo derived embryos, DNA methylation was removed from this intragenic DMR after fertilization, but partially replaced by the time the embryo reached the blastocyst stage. Among embryos developing in vivo, the level of DNA methylation was significantly lower in female than in male blastocysts. This sexual dimorphism was also found between parthenogenetic and androgenetic embryos, and followed the donor cell sex in SCNT derived blastocysts and is evidence for correct methylation reprogramming in SCNT embryos.

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Language(s): eng - English
 Dates: 2009-10-01
 Publication Status: Issued
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Title: Genomics
  Alternative Title : Genomics
Source Genre: Journal
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Pages: - Volume / Issue: 94 (1) Sequence Number: - Start / End Page: 63 - 69 Identifier: ISSN: 0888-7543