4.5 Article

MicroRNA-133b stimulates ovarian estradiol synthesis by targeting Foxl2

Journal

FEBS LETTERS
Volume 587, Issue 15, Pages 2474-2482

Publisher

WILEY
DOI: 10.1016/j.febslet.2013.06.023

Keywords

Granulosa cell; miR-133b; Foxl2; StAR; CYP19A1; Estrogen

Funding

  1. National Basic Research Program of China [2010CB945104]
  2. National Natural Science Foundation of China [81070508, 30900727, 81070492, 81170570]
  3. Health Department of Jiangsu Province [XK201102, LJ201102, RC2011005]
  4. Program of Six Top Talents of Jiangsu Province [2010-WS-058, 2012-WSN-005]

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Forkhead L2 (Foxl2) is expressed in ovarian granulosa cells and participates in steroidogenesis by transcriptionally regulating target genes such as steroidogenic acute regulatory protein (StAR) and CYP19A1. In this study, a direct link between microRNA-133b (miR-133b) and Foxl2-mediated estradiol release in granulosa cells was established. miR-133b was involved in follicle-stimulating hormone (FSH)-induced estrogen production. Luciferase assays confirmed that miR-133b was bound to the 3' untranslated region (3'UTR) of Foxl2 mRNA. Consistent with this finding, miR-133b overexpression reduced the Foxl2 levels. Furthermore, miR-133b inhibited Foxl2 binding to the StAR and CYP19A1 promoter sequences. These results demonstrate that miR-133b down-regulates Foxl2 expression in granulosa cells by directly targeting the 3'UTR, thus inhibiting the Foxl2-mediated transcriptional repression of StAR and CYP19A1 to promote estradiol production. Crown Copyright (C) 2013 Published by Elsevier B.V. on behalf of Federation of European Biochemical society. All rights reserved.

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