Chesters J K, Boyne R, Petrie L, Lipson K E
Rowett Research Institute, Aberdeen, Scotland, U.K.
Biochem J. 1995 Jun 1;308 ( Pt 2)(Pt 2):659-64. doi: 10.1042/bj3080659.
Previous studies had indicated that lack of Zn2+ inhibits the expression of thymidine kinase activity and produces a corresponding reduction in the concentration of its mRNA. The present investigations have shown that with human thymidine kinase this is associated with increased binding of a specific protein to the gene's promoter in the region between -55 and -83 bp 5' to the transcription initiation site. A second binding site for the protein is present within the sixth exon of the human thymidine kinase gene.
先前的研究表明,锌离子缺乏会抑制胸苷激酶活性的表达,并使其mRNA浓度相应降低。目前的研究表明,对于人类胸苷激酶而言,这与一种特定蛋白质与基因启动子在转录起始位点5'端-55至-83碱基对区域的结合增加有关。该蛋白质的第二个结合位点存在于人类胸苷激酶基因的第六个外显子内。