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PMID: 17143267 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

PGC7/Stella protects against DNA demethylation in early embryogenesis.

Nature cell biology ·Vol. 9 ·No. 1 ·2007-01-00 ·Pages 64-71

Nakamura T, Arai Y, Umehara H, Masuhara M, Kimura T, Taniguchi H, Sekimoto T, Ikawa M, Yoneda Y, Okabe M, Tanaka S, Shiota K, Nakano T

Abstract

DNA methylation is an important means of epigenetic gene regulation and must be carefully controlled as a prerequisite for normal early embryogenesis. Although global demethylation occurs soon after fertilization, it is not evenly distributed throughout the genome. Genomic imprinting and epigenetic asymmetry between parental genomes, that is, delayed demethylation of the maternal genome after fertilization, are clear examples of the functional importance of DNA methylation. Here, we show that PGC7/Stella, a maternal factor essential for early development, protects the DNA methylation state of several imprinted loci and epigenetic asymmetry. After determining that PGC7/Stella binds to Ran binding protein 5 (RanBP5; a nuclear transport shuttle protein), mutant versions of the two proteins were used to examine exactly when and where PGC7/Stella functions within the cell. It is likely that PGC7/Stella protects the maternal genome from demethylation only after localizing to the nucleus, where it maintains the methylation of several imprinted genes. These results demonstrate that PGC7/Stella is indispensable for the maintenance of methylation involved in epigenetic reprogramming after fertilization.

MeSH Terms
Animals COS Cells Cell Line Cell Nucleus/metabolism Chlorocebus aethiops Chromosomal Proteins, Non-Histone DNA Methylation Embryonic Development/genetics Epigenesis, Genetic Female Fertilization/genetics Gene Expression Regulation, Developmental Humans Male Mice Proteins/genetics,metabolism,physiology Transfection
Chemicals
Chromosomal Proteins, Non-Histone DPPA3 protein, human Proteins
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Nakamura Toshinobu
Department of Pathology, Graduate School of Medicine and Frontier Biosciences, Osaka University, Osaka 565-0871, Japan. tnakano@patho.med.osaka-u.ac.jp
Arai Yoshikazu
Umehara Hiroki
Masuhara Masaaki
Kimura Tohru
Taniguchi Hisaaki
Sekimoto Toshihiro
Ikawa Masahito
Yoneda Yoshihiro
Okabe Masaru
Tanaka Satoshi
Shiota Kunio
Nakano Toru
Article Info
Journal
Nature cell biology
Abbr.
Nat Cell Biol
ISSN
1465-7392
Published
2007-01-00
Epub
2006-00-03
Pages
64-71
Language
English
Region
England
NLM ID
100890575
Subset
IM
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