FIGLA, a basic helix-loop-helix transcription factor, balances sexually dimorphic gene expression in postnatal oocytes.

Journal:

Mol. Cell. Biol. 2010 Jul

Authors:

Hu W, Gauthier L, Baibakov B, Jimenez-Movilla M, Dean J

Abstract

Maintenance of sex-specific germ cells requires balanced activation and repression of genetic hierarchies to ensure gender-appropriate development in mammals. Figla (factor in the germ line, alpha) encodes a germ cell-specific basic helix-loop-helix transcription factor first identified as an activator of oocyte genes. In comparing the ovarian proteome of normal and Figla null newborn mice, 18 testis-specific or -enhanced proteins were identified that were more abundant in Figla null ovaries tha
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n in normal ovaries. Transgenic mice, ectopically expressing Figla in male germ cells, downregulated a subset of these genes and demonstrated age-related sterility associated with impaired meiosis and germ cell apoptosis. Testis-associated genes, including Tdrd1, Tdrd6, and Tdrd7, were suppressed in the transgenic males with a corresponding disruption of the sperm chromatoid body and mislocalization of MVH and MILI proteins, previously implicated in posttranscriptional processing of RNA. These data demonstrate that physiological expression of Figla plays a critical dual role in activation of oocyte-associated genes and repression of sperm-associated genes during normal postnatal oogenesis.[less]

Mesh Headings:

Animals, Animals, Newborn, Basic Helix-Loop-Helix Transcription Factors, Fatty Acids, Fatty Alcohols, Female, Gene Expression, Male, Mice, Mice, Knockout, Mice, Transgenic, Oocytes, Oogenesis, Ovary, RNA, Messenger, Recombinant Proteins, Sex Characteristics, Testis