[1] LINCOLN COLL,DEPT BIOCHEM & MICROBIOL,CANTERBURY,NEW ZEALAND
[2] BAYLOR COLL MED,DEPT PATHOL,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT PEDIAT,HOUSTON,TX 77030
来源:
AMERICAN JOURNAL OF PHYSIOLOGY
|
1991年
/
261卷
/
02期
关键词:
LUNG TUMORS;
PULMONARY EXPRESSION;
D O I:
10.1152/ajplung.1991.261.2.L70
中图分类号:
Q4 [生理学];
学科分类号:
071003 ;
摘要:
The rabbit uteroglobin gene is expressed in the lungs and reproductive tracts of male and female rabbits. To examine whether the promoter region of the uteroglobin gene could be used to target a heterologous gene to the lungs of transgenic mice, a fusion gene consisting of 3.3 kb of the 5'-flanking region of the rabbit uteroglobin gene and the large T antigen gene of the SV40 virus was constructed and microinjected into the pronuclei of one-cell mouse embryos. Eleven founder transgenic mice (5 female and 6 male) were generated. Seven of these mice developed bronchioalveolar neoplasms. Four of the founder males also developed primitive undifferentiated urogenital tract tumors. One founder female and one female offspring of a founder male developed glandular paraovarian tumors. Northern analysis revealed that the predominant site of expression of the transgene was the lung. Immunohistochemical staining showed T antigen predominantly in epithelial cells lining the bronchioles, the submucosal glands of the trachea, and the neoplasms. There appeared to be a high level of mosaicism for the transgene in the founder mice, with poor transmission of the transgene to subsequent generations. This suggest that, under the control of the uteroglobin promoter, the T antigen gene may be lethal to the fetus.