Meng Jie, Zhang Linlin, Li Li, Li Chunyan, Wang Ting, Zhang Guofan
Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, Shandong, China.
Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, Shandong, China.
Aquat Toxicol. 2015 Aug;165:179-88. doi: 10.1016/j.aquatox.2015.05.023. Epub 2015 May 29.
Oysters accumulate zinc at high tissue concentrations, and the metal response element (MRE)-binding transcription factor (MTF) functions as the cellular zinc sensor that coordinates the expression of genes involved in zinc efflux and storage, as well as those that protect against metal toxicity. In this study, we cloned MTF-1 in oysters and examined its regulation mechanism for its classic target genes, including MTs and ZnT1 under zinc exposure conditions. We cloned CgMTF-1 and determined the subcellular locations of its protein product in HEK293 cells. CgMTF-1 has a 2826bp open reading frame that encodes a predicted polypeptide with 707 amino acid residues, showing six well-conserved zinc finger domains that are required for metal binding. In HEK293 cell lines, CgMTF-1 primarily localizes in the cell nucleus under unstressed conditions and nuclear translocation was not critical for the activation of this gene. We searched for CgMTF-1-regulated genes in oysters using RNA interference. Decreased expression levels of CgMT1, CgMT4, and CgZnT1 were observed after CgMTF-1 interference (>70% inhibition) under zinc exposure, indicating the critical role of CgMTF-1 in the regulation of these genes. We searched for a direct regulation mechanism involving CgMTF-1 for CgMT1, CgMT4, and CgZnT1 in vitro. EMSA experiments indicated that CgMTF-1 can bind with the MREs found in the CgZnT1, CgMT1 and CgMT4 promoter regions. Additionally, luciferase reporter gene experiments indicated that CgMTF-1 could activate the CgMT1, CgMT4, and CgZnT1 promoters. Overall, our results suggest that CgMTF-1 directly coordinates the regulation of CgMTs and CgZnT1 expression and plays important roles in protecting oysters under zinc exposure conditions. To our knowledge, this is the first study to elucidate the function of MTF-1 in marine bivalves and provides new insights into the mechanisms of zinc accumulation and tolerance in mollusks.
牡蛎在组织中积累高浓度的锌,金属反应元件(MRE)结合转录因子(MTF)作为细胞锌传感器,协调参与锌外流和储存的基因以及那些抵御金属毒性的基因的表达。在本研究中,我们克隆了牡蛎中的MTF-1,并研究了其在锌暴露条件下对其经典靶基因(包括MTs和ZnT1)的调控机制。我们克隆了CgMTF-1并确定了其蛋白产物在HEK293细胞中的亚细胞定位。CgMTF-1有一个2826bp的开放阅读框,编码一个预测的含有707个氨基酸残基的多肽,显示出六个金属结合所需的高度保守的锌指结构域。在HEK293细胞系中,CgMTF-1在未受胁迫条件下主要定位于细胞核,核转位对该基因的激活并不关键。我们使用RNA干扰在牡蛎中寻找CgMTF-1调控的基因。在锌暴露条件下,CgMTF-1干扰后(抑制率>70%),观察到CgMT1、CgMT4和CgZnT1的表达水平降低,表明CgMTF-1在这些基因的调控中起关键作用。我们在体外寻找CgMTF-1对CgMT1、CgMT4和CgZnT1的直接调控机制。电泳迁移率变动分析(EMSA)实验表明,CgMTF-1可以与CgZnT1、CgMT1和CgMT4启动子区域中的MRE结合。此外,荧光素酶报告基因实验表明,CgMTF-1可以激活CgMT1、CgMT4和CgZnT1启动子。总体而言,我们的结果表明,CgMTF-1直接协调CgMTs和CgZnT1表达的调控,并在锌暴露条件下保护牡蛎方面发挥重要作用。据我们所知,这是第一项阐明MTF-1在海洋双壳贝类中的功能的研究,并为软体动物中锌积累和耐受机制提供了新的见解。