Birkenmeier E H, Hoppe P C, Lyford K A, Gwynn B
Jackson Laboratory, Bar Harbor, ME 04609.
Nucleic Acids Res. 1992 Jun 11;20(11):2819-25. doi: 10.1093/nar/20.11.2819.
Comparison of the promoter sequence for the sn-glycerol-3-phosphate dehydrogenase (GPDH, EC 1.1.1.8) genes in mice and humans showed that there were three promoter domains conserved in evolution (1). To study the functional organization of the GPDH promoter, we generated transgenic mice carrying the complete human gene, GPD1. The level of human and mouse GPDH activity was measured in each tissue and the amount of human-mouse GPDH heterodimer was used as a sensitive indicator of cell-specific expression of GPD1. During postnatal development and in adult tissues of the transgenic mice, human GPDH was expressed at levels that corresponded closely to the expression of the endogenous mouse gene, Gdc-1. Surprisingly, deletion of the evolutionarily conserved fat-specific elements (FSE) in the proximal promoter region failed to reveal any alterations in GPD1 expression that were specific for either white or brown adipose tissue.
对小鼠和人类甘油-3-磷酸脱氢酶(GPDH,EC 1.1.1.8)基因启动子序列的比较表明,在进化过程中有三个保守的启动子结构域(1)。为了研究GPDH启动子的功能组织,我们构建了携带完整人类基因GPD1的转基因小鼠。在每个组织中测量人类和小鼠GPDH的活性水平,并将人-鼠GPDH异二聚体的量用作GPD1细胞特异性表达的敏感指标。在转基因小鼠的出生后发育和成年组织中,人类GPDH的表达水平与内源性小鼠基因Gdc-1的表达密切相关。令人惊讶的是,近端启动子区域中进化保守的脂肪特异性元件(FSE)的缺失并未揭示GPD1表达在白色或棕色脂肪组织中存在任何特异性改变。