Literature DB >> 9299233

An oocyte-specific methylation imprint center in the mouse U2afbp-rs/U2af1-rs1 gene marks the establishment of allele-specific methylation during preimplantation development.

H Shibata1, T Ueda, M Kamiya, A Yoshiki, M Kusakabe, C Plass, W A Held, S Sunahara, M Katsuki, M Muramatsu, Y Hayashizaki.   

Abstract

An oocyte-specific methylation imprint mark region, consisting of approximately 200 bp from the mouse imprinted gene U2afbp-rs, was identified within an area containing a CpG island and a short tandem repeat sequence. The oocyte-specific methylation was preserved in fertilized eggs and then expanded on the repressed maternal allele during preimplantation development until the adult methylation pattern was achieved by 12.5 days of embryonic development. These results indicate that the oocyte-specific imprinting mark region acts as a center in establishing the hypermethylated region on the repressed maternal allele. Furthermore, a region that is hypermethylated in both gametes was identified but its hypermethylation was conserved only on the maternal allele during preimplantation development, suggesting that some factor(s) inherited from oocytes may act to maintain hypermethylation on the maternal allele. Copyright 1997 Academic Press.

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Year:  1997        PMID: 9299233     DOI: 10.1006/geno.1997.4877

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

1.  Parental allele-specific chromatin configuration in a boundary-imprinting-control element upstream of the mouse H19 gene.

Authors:  S Khosla; A Aitchison; R Gregory; N D Allen; R Feil
Journal:  Mol Cell Biol       Date:  1999-04       Impact factor: 4.272

2.  Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes.

Authors:  Cécile Fournier; Yuji Goto; Esteban Ballestar; Katia Delaval; Ann M Hever; Manel Esteller; Robert Feil
Journal:  EMBO J       Date:  2002-12-02       Impact factor: 11.598

3.  A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome.

Authors:  N J Smilinich; C D Day; G V Fitzpatrick; G M Caldwell; A C Lossie; P R Cooper; A C Smallwood; J A Joyce; P N Schofield; W Reik; R D Nicholls; R Weksberg; D J Driscoll; E R Maher; T B Shows; M J Higgins
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

4.  DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1.

Authors:  R I Gregory; T E Randall; C A Johnson; S Khosla; I Hatada; L P O'Neill; B M Turner; R Feil
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

5.  Parent-of-origin-specific binding of nuclear hormone receptor complexes in the H19-Igf2 imprinting control region.

Authors:  Piroska E Szabó; Gerd P Pfeifer; Jeffrey R Mann
Journal:  Mol Cell Biol       Date:  2004-06       Impact factor: 4.272

6.  Gatekeeper of pluripotency: a common Oct4 transcriptional network operates in mouse eggs and embryonic stem cells.

Authors:  Maurizio Zuccotti; Valeria Merico; Michele Bellone; Francesca Mulas; Lucia Sacchi; Paola Rebuzzini; Alessandro Prigione; Carlo A Redi; Riccardo Bellazzi; James Adjaye; Silvia Garagna
Journal:  BMC Genomics       Date:  2011-07-05       Impact factor: 3.969

  6 in total

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