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Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells.

Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Research Abstract Details 

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  • Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Abstract Text:

    kazuhiro iwahashiKazuhiro Iwahashi,hirotaka yoshiokaHirotaka Yoshioka,eleanor w lowEleanor W Low,john r mccarreyJohn R McCarrey,ryuzo yanagimachiRyuzo Yanagimachi,yukiko yamazakiYukiko Yamazaki,

    In mice, unique events regulating epigenetic programming (e.g., genomic imprinting) and replication state (mitosis versus meiosis) occur during fetal germ cell development. To determine whether these processes are autonomously programmed in fetal germ cells or are dependent upon ongoing instructive interactions with surrounding gonadal somatic cells, we isolated male and female germ cells at 13.5 days postcoitum (dpc) and maintained them in culture for 6 days, either alone or in the presence of feeder cells or gonadal somatic cells. We examined allele-specific DNA methylation in the imprinted H19 and Snrpn genes, and we also determined whether these cells remained mitotic or entered meiosis. Our results show that isolated male germ cells are able to establish a characteristic "paternal" methylation pattern at imprinted genes in the absence of any support from somatic cells. On the other hand, cultured female germ cells maintain a hypomethylated status at these loci, characteristic of the normal "maternal" methylation pattern in endogenous female germ cells before birth. Further, the surviving female germ cells entered first meiotic prophase and reached the pachytene stage, whereas male germ cells entered mitotic arrest. These results indicate that mechanisms controlling both epigenetic programming and replication state are autonomously regulated in fetal germ cells that have been exposed to the genital ridge prior to 13.5 dpc.

    Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Publishing Authors By Initials

    k iwahashiK Iwahashi,h yoshiokaH Yoshioka,ew lowEW Low,jr mccarreyJR McCarrey,r yanagimachiR Yanagimachi,y yamazakiY Yamazaki,

    For similar reproductive and urinary physiology: reproduction: sexual development research abstracts see: reproductive and urinary physiology: reproduction: sexual development research

    PUBMED ID PMID:

    MEDLINE DATE:

    Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Biology of reproduction

    VOLUME: 77

    Page Numbers: 697-706

    Journal Abbreviation: Biol. Reprod.

    ISSN: 0006-3363

    DAY: 5

    MONTH: 07

    YEAR: 2007

    Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 207224

    Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Keywords Mesh Terms:

    KEYWORDS: Sexual Development

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells. Information

    Substance Name: DNA (Cytosine-5-)-Methyltransferase

    Registry Number: EC 2.1.1.37

    Grant and Affiliation Information for Autonomous regulation of sex-specific developmental programming in mouse fetal germ cells.

    AFFILIATION: Institute for Biogenesis Research, John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii 96813, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCRR

    GRANT: P20RR16467

    ACRONYM: RR

    MEDLINETA: Biol Reprod

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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