| Literature DB >> 19917504 |
Ikuko K Bentsi-Barnes1, Fang-Ting Kuo, Gillian M Barlow, Margareta D Pisarska.
Abstract
FOXL2 is expressed in granulosa cells (GC) of small and medium ovarian follicles, functions as a repressor of the human steroidogenic acute regulatory gene, a marker of a GC differentiation, and its mutation is associated with premature ovarian failure (POF) in women with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), type I. We now report that FOXL2 also represses the transcription of aromatase, P450scc, and cyclin D2, three other key genes involved in GC proliferation, differentiation, and steroidogenesis, and that a FOXL2 mutation found in patients with BPES type I, also fails to repress aromatase transcription, further supporting a role for FOXL2 in follicle maturation. Copyright (c) 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.Entities:
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Year: 2009 PMID: 19917504 PMCID: PMC2876195 DOI: 10.1016/j.fertnstert.2009.09.050
Source DB: PubMed Journal: Fertil Steril ISSN: 0015-0282 Impact factor: 7.329