Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure

Reproductive BioMedicine Online

Volumn 20, Issue 4, 2010, Pages 499-503

  Wang, Binbin ^a,b   Mu, Yuan ^a,b   Ni, Feng ^c   Zhou, Sirui ^a,b   Wang, Jing ^a,b   Cao, Yunxia ^c   Ma, Xu ^a,b,d  

^a GRADUATE SCHOOL OF PEKING UNION MEDICAL COLLEGE   (China)

^b NATIONAL RESEARCH INSTITUTE FOR FAMILY PLANNING   (China)

^c ANHUI MEDICAL UNIVERSITY   (China)

^d WORLD HEALTH ORGANIZATION   (Switzerland)

Author keywords

Female infertility; FOXO3; Premature ovarian failure

Indexed keywords

ALANINE; ASPARAGINE; ASPARTIC ACID; FOXO3 PROTEIN; GLYCINE; HISTIDINE; LEUCINE; PHENYLALANINE; PROLINE; PROTEIN; SERINE; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; APOPTOSIS; ARTICLE; CELL ACTIVATION; CHINESE; CONTROLLED STUDY; FEMALE; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; OOCYTE; OVARY FOLLICLE; PREMATURE OVARIAN FAILURE; SAMPLE; SCREENING; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 77951653109     PISSN: 14726483     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rbmo.2010.01.008     Document Type: Article

References (25)

1. Aittomaeki, K., Dieguez Lucena, J., Pakarinen, P., et al., 1995. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 82, 958-959.
2. Bione, S., Sala, C., Manzini, C., et al., 1998. A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. Am. J. Hum. Genet. 62, 533-541.
3. Board, J., Redwine, F., Moncure, C., Frable, W., Taylor, J., 1979. Identification of differing etiologies of clinically diagnosed premature menopause. Am. J. Obstet. Gynecol. 134, 936-944.
4. Castrillon, D., Miao, L., Kollipara, R., Horner, J., DePinho, R., 2003. Suppression of ovarian follicle activation in mice by the transcription factor Foxo3a. Science 301, 215-218. (Pubitemid 36858475)
5. Coulam, C., Adamson, S., Annegers, J., 1986. Incidence of premature ovarian failure. Obstet. Gynecol. 67, 604-606.
6. Dixit, H., Rao, L.K., Padmalatha, V.V., et al., 2006. Missense mutations in the BMP15 gene are associated with ovarian failure. Hum. Genet. 119 (4), 408-415.
7. Elvin, J.A., Matzuk, M.M., 1998. Mouse models of ovarian failure. Rev. Reprod. 3 (3), 183-195.
8. Gallardo, T.D., John, G.B., Bradshaw, K., et al., 2008. Sequence variation at the human FOXO3 locus: a study of premature ovarian failure and primary amenorrhea. Hum. Reprod. 23, 216-221.
9. Hosaka, T., Biggs, W., Tieu, D., et al., 2004. Disruption of forkhead transcription factor (FOXO) family members in mice reveals their functional diversification. Proc. Natl. Acad. Sci. USA 101, 2975-2980.
10. John, G.B., Shirley, LJ., Gallardo, T.D., Castrillon, D.H., 2007a. Specificity of the requirement for Foxo3 in primordial follicle activation. Reproduction 133, 855-863.
11. John, G.B., Shirley, L.J., Gallardo, T.D., Castrillon, D.H., 2007b. Specificity of the requirement for Foxo3 in primordial follicle activation. Reproduction 133, 855-863.
12. Kalataridou, S., Nelson, L., 2000. Premature ovarian failure is not premature menopause. Ann. NY Acad. Sci. 900, 393-402.
13. Luborsky, J., Meyer, P., Sowers, M., Gold, E., Santoro, N., 2003. Premature menopause in a multi-ethnic population study of the menopause transition. Hum. Reprod. 18, 199-206.
14. McGee, E., Hsueh, A., 2000. Initial and cyclic recruitment of ovarian follicles. Endocr. Rev. 21, 200-214.
15. McKinlay, S., Jefferys, M., Thompson, B., 1972. An investigation of the age at menopause. J. Biosoc. Sci. 4, 161-173.
16. Mei, Yang, Zhang, Yiru, Yamamoto, Kazuo, Xie, Wei, Mak, Tak W., You, Han, 2009. FOX03a-dependent regulation of Pink1 (Park6) mediates survival signaling in response to cytokine deprivation. PNAS 106 (13), 5153-5158.
17. Russell, P., Bannatyne, P., Shearman, R., Fraser, I., Corbett, P., 1982. Premature hypergonadotropic ovarian failure: clinicopathological study of 19 cases. Int. J. Gynecol. Pathol. 1, 185.
18. Tilly, J., 2001. Commuting the death sentence: how oocytes strive to survive. Nat. Rev. Mol. Cell Biol. 2, 838.
19. Timmreck, L., Reindollar, R., 2003. Contemporary issues in primary amenorrhea. Obstet. Gynecol. Clin. North Am. 30, 287-302.
20. van Kasteren, Y., Hundscheid, R., Smits, A., Cremers, F., van Zonneveld, P., Braat, D., 1999. Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease? Hum. Reprod. 14, 2455-2459. (Pubitemid 29473910)
21. Vegetti, W., 1998. Inheritance in idiopathic premature ovarian failure: analysis of 71 cases. Hum. Reprod. 13, 1796-1800.
22. Wang, Binbin, Zhou, Sirui, Yang, Ze, et al., 2008. Genetic analysis of tumor necrosis factor-α (TNF-α) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease. J. Neurol. Sci. 270 (1-2), 148-151.
23. Watkins, W., Umbers, A., Woad, K., et al., 2006. Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure. Fertil. Steril. 86, 1518-1521.
24. Wyshak, G., Frisch, R., 1982. Evidence for a secular trend in age of menarche. N. Engl. J. Med. 306, 1033-1035.
25. Zarate, A., Karchmer, S., Gomez, E., Castelazo-Ayala, L., 1970. Premature menopause. A clinical, histologic and cytogenetic study. Am. J. Obstet. Gynecol. 106, 110-114.