Ledent C, Parmentier M, Vassart G
Institut de Recherche Interdisciplinaire en Biologie Humaine et Nucléaire, Université Libre de Bruxelles, Belgium.
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6176-80. doi: 10.1073/pnas.87.16.6176.
Fusion genes containing 1600 or 2000 base pairs of the bovine thyroglobulin gene 5' flanking region and the chloramphenicol acetyltransferase (CAT) coding sequence were constructed and used to generate transgenic mice. Altogether, 24 independent transgenic lines were obtained, and the expression of the transgene was assayed by measuring the CAT activity in different tissues. Depending on the transgenic lines, the fusion gene was either silent in all tissues or specifically expressed in the thyroid. The level of expression was found to be highly variable from one line to another and to be regulated by thyrotropin in a manner similar to the natural thyroglobulin gene. The methylation status of the integrated DNA was tested by digestion of DNA extracted from thyroid and other tissues with the isochizomers Msp I and Hpa II. It was found that one of the Hpa II sites was demethylated specifically in the thyroid.
构建了含有1600或2000个碱基对的牛甲状腺球蛋白基因5'侧翼区和氯霉素乙酰转移酶(CAT)编码序列的融合基因,并用于产生转基因小鼠。总共获得了24个独立的转基因系,并通过测量不同组织中的CAT活性来检测转基因的表达。根据转基因系的不同,融合基因在所有组织中均无活性,或在甲状腺中特异性表达。发现表达水平在不同品系之间高度可变,并受促甲状腺激素的调节,其方式类似于天然甲状腺球蛋白基因。通过用同裂酶Msp I和Hpa II消化从甲状腺和其他组织中提取的DNA,检测整合DNA的甲基化状态。发现其中一个Hpa II位点在甲状腺中特异性去甲基化。