Fertility and Sterility
Volume 94, Issue 1 , Pages 353-356, June 2010

Human forkhead L2 represses key genes in granulosa cell differentiation including aromatase, P450scc, and cyclin D2

  • Ikuko K. Bentsi-Barnes, Ph.D.

      Affiliations

    • Division of Reproductive Endocrinology and Infertility, Department of Obstetrics/Gynecology, Cedars-Sinai Medical Center, Los Angeles, California
  • ,
  • Fang-Ting Kuo, Ph.D.

      Affiliations

    • Division of Reproductive Endocrinology and Infertility, Department of Obstetrics/Gynecology, Cedars-Sinai Medical Center, Los Angeles, California
  • ,
  • Gillian M. Barlow, Ph.D.

      Affiliations

    • Division of Reproductive Endocrinology and Infertility, Department of Obstetrics/Gynecology, Cedars-Sinai Medical Center, Los Angeles, California
  • ,
  • Margareta D. Pisarska, M.D.

      Affiliations

    • Division of Reproductive Endocrinology and Infertility, Department of Obstetrics/Gynecology, Cedars-Sinai Medical Center, Los Angeles, California
    • David Geffen School of Medicine, UCLA, Los Angeles, California
    • Corresponding Author InformationReprint requests: Margareta D. Pisarska, M.D., Center of Fertility and Reproductive Medicine, Division of REI, Department of Ob/Gyn, Cedars-Sinai Medical Center, 8635 West Third Street, Suite 160W, Los Angeles, CA 90048 (FAX: 310-423-0140).

Received 29 May 2009; received in revised form 15 September 2009; accepted 23 September 2009. published online 16 November 2009.

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.

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 I.K.B.-B. has nothing to disclose. F.-T.K. has nothing to disclose. G.M.B. has nothing to disclose. M.D.P. has nothing to disclose.

 Supported by grant R01HD047603 from the National Institute of Child Health and Human Development and the Office of Research on Women's Health, Bethesda, Maryland (M.D.P.) and by a grant from the Helping Hands of Los Angeles, Inc., Los Angeles, California (M.D.P.).

PII: S0015-0282(09)03800-X

doi:10.1016/j.fertnstert.2009.09.050

Fertility and Sterility
Volume 94, Issue 1 , Pages 353-356, June 2010