FIGα, a germ cell-specific transcription factor required for ovarian follicle formation

生物 生殖细胞 转录因子 卵泡发生 卵泡 细胞生物学 毛囊 男科 遗传学 卵巢 内分泌学 胚胎发生 基因 胚胎 医学
作者
Selma M. Soyal,Asma Amleh,Jurrien Dean
出处
期刊:Development [The Company of Biologists]
卷期号:127 (21): 4645-4654 被引量:494
标识
DOI:10.1242/dev.127.21.4645
摘要

Primordial follicles are formed perinatally in mammalian ovaries and at birth represent the lifetime complement of germ cells. With cyclic periodicity, cohorts enter into a growth phase that culminates in ovulation of mature eggs, but little is known about the regulatory cascades that govern these events. FIGalpha, a transcription factor implicated in postnatal oocyte-specific gene expression, is detected as early as embryonic day 13. Mouse lines lacking FIGalpha were established by targeted mutagenesis in embryonic stem cells. Although embryonic gonadogenesis appeared normal, primordial follicles were not formed at birth, and massive depletion of oocytes resulted in shrunken ovaries and female sterility. Fig(&agr;) (the gene for FIGalpha null males have normal fertility. The additional observation that null females do not express Zp1, Zp2 or Zp3 indicates that FIGalpha plays a key regulatory role in the expression of multiple oocyte-specific genes, including those that initiate folliculogenesis and those that encode the zona pellucida required for fertilization and early embryonic survival. The persistence of FIGalpha in adult females suggests that it may regulate additional pathways that are essential for normal ovarian development.

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