THE MULTIDRUG RESISTANCE AND CYSTIC-FIBROSIS GENES HAVE COMPLEMENTARY PATTERNS OF EPITHELIAL EXPRESSION

被引:178
作者
TREZISE, AEO
ROMANO, PR
GILL, DR
HYDE, SC
SEPULVEDA, FV
BUCHWALD, M
HIGGINS, CF
机构
[1] HOSP SICK CHILDREN,RES INST,DEPT GENET,TORONTO M5G 1X8,ONTARIO,CANADA
[2] AFRC,INST ANIM PHYSIOL & GENET RES,CAMBRIDGE CB2 4AT,ENGLAND
关键词
CYSTIC FIBROSIS; GENE EXPRESSION; INSITU HYBRIDIZATION; MULTIDRUG RESISTANCE; P-GLYCOPROTEIN;
D O I
10.1002/j.1460-2075.1992.tb05528.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cystic fibrosis gene product, CFTR, and the multidrug resistance P-glycoprotein (encoded by the MDR1 gene) are structurally related proteins and both are associated with epithelial chloride channel activities. We have compared their cell-specific expression in the rat by in situ hybridization. In all tissues examined the two genes were found to have complementary patterns of expression, demonstrating exquisite regulation in both cell-specific and temporal fashions. Additionally, a switch in expression from one gene to the other was observed in certain tissues. For example, expression in the intestine switches from CFTR to MDR1 as the cells migrate across the crypt-villus boundary. A switch from CFTR to MDR1 expression was also observed in the uterine epithelium upon pregnancy. These data suggest that CFTR and P-glycoprotein serve analogous roles in epithelial cells and provide additional evidence that P-glycoprotein has a physiological role in regulating epithelial cell volume. The patterns of expression suggest that the regulation of these two genes is coordinately controlled.
引用
收藏
页码:4291 / 4303
页数:13
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