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Fertility Center of CHA General Hospital,3 CHA Research Institute, Pochon CHA University, Seoul 135–081, Republic of Korea
Department of Obstetrics and Gynecology,4 Baylor College of Medicine, Houston, Texas 77030
ABSTRACT
We previously discovered a germ cell-specific spermatogenesis and oogenesis basic helix-loop-helix transcription factor, Sohlh2. We generated Sohlh2-deficient mice to understand physiologic consequences of Sohlh2 deletion. We discovered that Sohlh2-knockout adult female mice are infertile due to lack of ovarian follicles. Sohlh2-deficient ovaries can form primordial follicles and, despite limited oocyte growth, do not differentiate surrounding granulosa cells into cuboidal and multilayered structures. Oocytes are rapidly lost in Sohlh2-deficient ovaries, and few are present by 14 days of postnatal life. However, the primordial oocytes are abnormal at the molecular level because they misexpress numerous germ cell- and oocyte-specific genes, including Sohlh1, Nobox, Figla, Gdf9, Pou5f1, Zp1, Zp3, Kit, Oosp1, Nlrp14, H1foo, and Stra8. Our findings show that Sohlh2 is a critical factor for maintenance and differentiation of the oocyte during early oogenesis.
oocyte development, oogenesis, primordial follicle, Sohlh2, transcription factor
1Supported by the National Institutes of Health Grant HD44858, and March of Dimes grant #6-FY08-313.
Correspondence: 2Aleksandar Rajkovic, Department of Obstetrics and Gynecology, Baylor College of Medicine, 1709 Dryden Road, Suite 1100, Houston, TX 77030. FAX: 713 798 2744; e-mail: rajkovic{at}bcm.edu
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