Ovulation Control

In mammals, the ability of a female to remain fertile depends on the continuous activation of oocyte-containing follicles from their dormant state in the ovary. Menopause, or the natural end of the female reproductive cycle, occurs when the primordial follicle pool has been exhausted. However, the molecular mechanisms underlying follicle activation have been poorly understood. Now, in a report that Pten, a gene best known for its role as a tumor suppressor, plays a vital role in regulating this process. The researchers showed that in genetically engineered mice lacking PTEN in their oocytes, the entire pool of immature eggs is activated prematurely, depleting the supply of mature, fertilizable eggs by early adulthood -- a situation similar to that of premature ovarian failure in humans. As noted by J. Marx, whether mutations in PTEN or in other proteins that cooperate with PTEN are involved in human ovarian problems remains to be determined. If so, the new findings may aid the design of improved fertility treatments.

 

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