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NOBOX is a key FOXL2 partner involved in ovarian folliculogenesis Free
Justine Bouilly1,2, Reiner A. Veitia3,4, and Nadine Binart1,2,*
1Inserm U693, Le Kremlin-Bicêtre, F-94276, France
2Univ Paris-Sud, Faculté de Médecine Paris-Sud, UMR-S693, Le Kremlin-Bicêtre, F-94276, France
3Institut Jacques Monod, Paris, France
4Univ Paris Diderot, Paris, France *Correspondence to:Nadine Binart, E-mail: nadine.binart@inserm.fr
J Mol Cell Biol, Volume 6, Issue 2, April 2014, 175-177,  https://doi.org/10.1093/jmcb/mju006

Dear Editor,

Early ovarian expression of Newborn oogenesis homeobox (NOBOX), a transcription factor belonging to the homeoprotein class, is decisive for the progression of primordial follicles to the primary follicular stage as demonstrated by the sterility of Nobox−/− female mice (Rajkovic et al., 2004). Consequently, the loss of the Nobox gene causes primary ovarian insufficiency (POI) (Rajkovic et al., 2004) and we have shown that 6.2% of POI cases harbor mutations in the NOBOX gene (Qin et al., 2007; Bouilly et al., 2011). Such a high prevalence of mutations demonstrates that NOBOX is a major autosomal gene involved in POI (Bouilly et al., 2011). However, the exact role of this transcription factor during folliculogenesis is unclear.