Characterization of mice deficient in aromatase (ArKO) because of targeted disruption of the cyp19 gene

被引:725
作者
Fisher, CR
Graves, KH
Parlow, AF
Simpson, ER
机构
[1] Prince Henrys Inst Med Res, Melbourne, Vic 3168, Australia
[2] Univ Texas, SW Med Ctr, Cecil H & Ida Green Ctr Reprod Biol Sci, Dallas, TX 75235 USA
[3] Univ Calif Los Angeles, Harbor Med Ctr, Torrance, CA 90509 USA
关键词
D O I
10.1073/pnas.95.12.6965
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The formation of estrogens from C-19 steroids is catalyzed by aromatase cytochrome P450 (P350arom), the product of the cyp19 gene. The actions of estrogen include dimorphic anatomical, functional, and behavioral effects on the development of both males and females, considerations that prompted us to examine the consequences of deficiency of aromatase activity in mice, Mice lacking a functional aromatase enzyme (ArKO) were generated by targeted disruption of the cyp19 gene. Male and female ArKO mice were born with the expected Mendelian frequency from F-1 parents and grew to adulthood. Female ArKO mice at 9 weeks of age displayed underdeveloped external genitalia and uteri. Ovaries contained numerous follicles with abundant granulosa cells and evidence of antrum formation that appeared arrested before ovulation. No corpora lutea were present. Additionally the stroma were hyperplastic with structures that appeared to be atretic follicles, Development of the mammary glands approximated that of a prepubertal female. Examination of male ArKO mite of the same age revealed essentially normal internal anatomy but with enlargement of the male accessory sex glands because of increased content of secreted material. The testes appeared normal. Male ArKO mice are capable of breeding and produce litters of approximately average size. Whereas serum estradiol levels were at the limit of detection, testosterone levels were elevated, as were the levels of follicle-stimulating hormone and luteinizing hormone, The phenotype of these animals differs markedly from that of the previously reported ERKO mice, in which the estrogen receptor alpha is deleted bp targeted disruption.
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页码:6965 / 6970
页数:6
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