Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2011 Apr;152(4):1199-208.
doi: 10.1210/en.2010-1041. Epub 2011 Jan 19.

Minireview: roles of the forkhead transcription factor FOXL2 in granulosa cell biology and pathology

Affiliations
Review

Minireview: roles of the forkhead transcription factor FOXL2 in granulosa cell biology and pathology

Margareta D Pisarska et al. Endocrinology. 2011 Apr.

Abstract

The forkhead transcription factor (FOXL2) is an essential transcription factor in the ovary. It is important in ovarian development and a key factor in female sex determination. In addition, FOXL2 plays a significant role in the postnatal ovary and follicle maintenance. The diverse transcriptional activities of FOXL2 are likely attributable to posttranslational modifications and binding to other key proteins involved in granulosa cell function. Mutations of FOXL2 lead to disorders of ovarian function ranging from premature follicle depletion and ovarian failure to unregulated granulosa cell proliferation leading to tumor formation. Thus, FOXL2 is a key regulator of granulosa cell function and a master transcription factor in these cells.

PubMed Disclaimer

Figures

Fig. 1.
Fig. 1.
Activity of FOXL2 as a transcriptional repressor. FOXL2 likely functions as a dimer (118) and requires sumoylation and phosphorylation for its activity. Other factors that may make up the transcriptional complex (Erα, SF-1, and DP103) are indicated, as are the genes known to be regulated by FOXL2. The effects of FOXL2 on gene transcription may differ depending on the stage of ovarian development, including sexual differentiation, granulosa cell development, and pathological states such as GCT formation.

Similar articles

Cited by

References

    1. Weigel D, Jurgens G, Kuttner F, Seifert E, Jackle H. 1989. The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo. Cell 57:645–658 - PubMed
    1. Lehmann OJ, Sowden JC, Carlsson P, Jordan T, Bhattacharya SS. 2003. Fox's in development and disease. Trends Genet 19:339–344 - PubMed
    1. Mahlapuu M, Ormestad M, Enerback S, Carlsson P. 2001. The forkhead transcription factor Foxf1 is required for differentiation of extra-embryonic and lateral plate mesoderm. Development 128:155–166 - PubMed
    1. Nakae J, Kitamura T, Kitamura Y, Biggs WH, 3rd, Arden KC, Accili D. 2003. The forkhead transcription factor Foxo1 regulates adipocyte differentiation. Dev Cell 4:119–129 - PubMed
    1. Brissette JL, Li J, Kamimura J, Lee D, Dotto GP. 1996. The product of the mouse nude locus, Whn, regulates the balance between epithelial cell growth and differentiation. Genes Dev 10:2212–2221 - PubMed

Publication types