Samson S L, Gedamu L
Department of Biological Sciences, University of Calgary, Alberta, Canada.
J Biol Chem. 1995 Mar 24;270(12):6864-71. doi: 10.1074/jbc.270.12.6864.
In this study, the contributions of the two metal-responsive elements (MREs) of the rainbow trout (Salmo gairdnerii) metallothionein (tMT)-B gene promoter (-137 to +5) were analyzed. The effect of MRE mutations on the basal and zinc-induced activities of tMT-B promoter-reporter gene fusions were determined by transfection of a rainbow trout hepatoma (RTH-149) cell line. Together, MREa and MREb cooperate to elicit a significant response to zinc but exhibit differential basal and metal-induced activity. The MREa sequence (-62 to -51) is important for basal promoter activity and can function independently, whereas the more distal MREb (-89 to -100) mainly contributes to metal induction through cooperative interactions with MREa. The degree of basal character of the MREs is partially determined by nucleotide differences at the flexible position N of the MRE consensus TGC(G/A)CNC. In mouse L and HepG2 cells, MREa activity is conserved, but the contributions of the MREb region differ, including reduced cooperativity with MREa. There are also differences in the apparent molecular masses of the rainbow trout and mammalian nuclear factors that bind to the tMT-B promoter and MREa sequence.
在本研究中,分析了虹鳟(Salmo gairdnerii)金属硫蛋白(tMT)-B基因启动子(-137至+5)的两个金属反应元件(MREs)的作用。通过转染虹鳟肝癌(RTH-149)细胞系,确定了MRE突变对tMT-B启动子-报告基因融合体的基础活性和锌诱导活性的影响。MREa和MREb共同作用以引发对锌的显著反应,但表现出不同的基础活性和金属诱导活性。MREa序列(-62至-51)对基础启动子活性很重要且可独立发挥作用,而更远端的MREb(-89至-100)主要通过与MREa的协同相互作用促进金属诱导。MREs的基础特性程度部分由MRE共有序列TGC(G/A)CNC的柔性位置N处的核苷酸差异决定。在小鼠L细胞和HepG2细胞中,MREa活性保守,但MREb区域的作用不同,包括与MREa的协同性降低。与tMT-B启动子和MREa序列结合的虹鳟和哺乳动物核因子的表观分子量也存在差异。