Petropoulos C J, Rosenberg M P, Jenkins N A, Copeland N G, Hughes S H
BRI-Basic Research Program, National Cancer Institute-Frederick Cancer Research Facility, Maryland 21701-1013.
Mol Cell Biol. 1989 Sep;9(9):3785-92. doi: 10.1128/mcb.9.9.3785-3792.1989.
We have generated transgenic mouse lines that carry the promoter region of the chicken skeletal muscle alpha (alpha sk) actin gene linked to the bacterial chloramphenicol acetyltransferase (CAT) gene. In adult mice, the pattern of transgene expression resembled that of the endogenous alpha sk actin gene. In most of the transgenic lines, high levels of CAT activity were detected in striated muscle (skeletal and cardiac) but not in the other tissues tested. In striated muscle, transcription of the transgene was initiated at the normal transcriptional start site of the chicken alpha sk actin gene. The region from nucleotides -191 to +27 of the chicken alpha sk actin gene was sufficient to direct the expression of CAT in striated muscle of transgenic mice. These observations suggest that the mechanism of tissue-specific actin gene expression is well conserved in higher vertebrate species.
我们已培育出携带与细菌氯霉素乙酰转移酶(CAT)基因相连的鸡骨骼肌α(α sk)肌动蛋白基因启动子区域的转基因小鼠品系。在成年小鼠中,转基因表达模式类似于内源性α sk肌动蛋白基因的表达模式。在大多数转基因品系中,在横纹肌(骨骼肌和心肌)中检测到高水平的CAT活性,但在其他测试组织中未检测到。在横纹肌中,转基因的转录在鸡α sk肌动蛋白基因的正常转录起始位点开始。鸡α sk肌动蛋白基因从核苷酸-191至+27的区域足以指导转基因小鼠横纹肌中CAT的表达。这些观察结果表明,组织特异性肌动蛋白基因表达机制在高等脊椎动物物种中得到了很好的保留。