Analysis of a 762-bp proximal leptin promoter to drive and control regulation of transgene expression of growth hormone receptor in mice

被引:7
作者
Chen, XL [1 ]
Hartzell, DL
McGraw, RA
Hausman, GJ
Dean, RG
Lee, K
Baile, CA
机构
[1] Univ Georgia, Dept Anim & Dairy Sci, Athens, GA 30602 USA
[2] Univ Georgia, Dept Physiol & Pharmacol, Athens, GA 30602 USA
[3] ARS, USDA, Athens, GA 30602 USA
关键词
transgenic; leptin; promoter; mice;
D O I
10.1006/bbrc.1999.1176
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
Transgenic (TG) mice expressing porcine GH receptor (pGHR) directed by a 762-bp proximal leptin promoter were used to analyze the capability of the promoter to drive and regulate pGHR expression in vivo. Transgene expression occurred in inguinal, retroper itoneal, and epididymal/parametrial fat depots in both male and female TG mice, but not in wild type (WT) mice. pGHR transgene was also expressed in liver, heart, kidney, muscle, lung, and brain. Levels of pGHR transgene mRNA were higher in tissues other than adipose tissue. Fasting reduced leptin mRNA levels in adipose; however, pGHR transgene expression was not affected in either adipose or muscle. These results suggest (1) the region between +3 and -759 bp of the leptin promoter is able to drive gene expression in vivo, (2) this region may not be responsible for adipose tissue specificity of leptin expression, and (3) this region may not be responsible for negative regulation of leptin gene expression during fasting. (C) 1999 Academic Press.
引用
收藏
页码:187 / 192
页数:6
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