A MUTATION IN THE POU-HOMEODOMAIN OF PIT-1 RESPONSIBLE FOR COMBINED PITUITARY-HORMONE DEFICIENCY

被引:357
作者
RADOVICK, S
NATIONS, M
DU, YF
BERG, LA
WEINTRAUB, BD
WONDISFORD, FE
机构
[1] RAINBOW BABIES & CHILDRENS HOSP,DEPT PEDIAT,DIV ENDOCRINOL,CLEVELAND,OH 44106
[2] CASE WESTERN RESERVE UNIV,SCH MED,CLEVELAND,OH 44106
[3] UNIV HOSP CLEVELAND,DEPT MED,DIV ENDOCRINOL & HYPERTENS,CLEVELAND,OH 44106
[4] NIDDKD,MOLEC & CELLULAR ENDOCRINOL BRANCH,BETHESDA,MD 20892
关键词
D O I
10.1126/science.257.5073.1115
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
Pit-1 is a pituitary-specific transcription factor responsible for pituitary development and hormone expression in mammals. Mutations in the gene encoding Pit-1 have been found in two dwarf mouse strains displaying hypoplasia of growth hormone, prolactin, and thyroid-stimulating, hormone-secreting cell types in the anterior pituitary. A point mutation in this gene was identified on one allele in a patient with combined pituitary hormone deficiency. Mutant Pit-1 binds DNA normally but acts as a dominant inhibitor of Pit-1 action in the pituitary.
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页码:1115 / 1118
页数:4
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