College of Life Science, key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, Nanchang University, Nanchang 330031, China.
College of Life Science, key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, Nanchang University, Nanchang 330031, China; Science&Technology Normal University of Jiangxi, Nanchang 330013, China.
Gene. 2018 Jun 20;660:51-61. doi: 10.1016/j.gene.2018.03.041. Epub 2018 Mar 15.
The small Mafs, MafF, MafG and MafK play critical roles in morphogenesis and homeostasis through associating with Cap "n" Collar family of transcription factors. In this study, we tried to identify a small Maf protein in the freshwater mussel Cristaria plicata. The MafK cDNA of C. plicata, designated as CpMafK, was cloned from the hemocytes using degenerate primers by the rapid amplification of cDNA ends PCR. The full length cDNA of CpMafK is 2170 bp, which includes an open reading frame of 570 bp, encoding 189 amino acids. CpMafK possesses four conserved domains and shows a low level (54-63%) of sequence similarity to small Mafs from other species. The results of Real-time quantitative PCR revealed that CpMafK mRNA was constitutively expressed in tissues, and the highest expression level was in hepatopancreas. After microcystin challenge, the expression levels of CpMafK mRNA were up-regulated in hemocytes and hepatopancreas. The cDNA of CpMafK was cloned into the plasmid pET-32, and the recombinant protein was expressed in Escherichia coli BL21(DE3). CpMafK could combine to the promoters of CpGST1 and CpGST2 with high-affinity in vitro. Therefore, CpMafK could regulate the expression of detoxification.
小 mafs(MafF、MafG 和 MafK)通过与 Cap'n'Colla 家族转录因子结合,在形态发生和内稳态中发挥关键作用。在本研究中,我们试图从淡水贻贝褶纹冠蚌中鉴定一种小 maf 蛋白。褶纹冠蚌 mafK cDNA,命名为 CpMafK,是通过 cDNA 末端快速扩增聚合酶链式反应,使用简并引物从血细胞中克隆得到的。CpMafK 的全长 cDNA 为 2170bp,包含一个 570bp 的开放阅读框,编码 189 个氨基酸。CpMafK 具有四个保守结构域,与其他物种的小 mafs 具有较低的序列相似性(54-63%)。实时定量 PCR 的结果显示,CpMafK mRNA 在组织中持续表达,在肝胰腺中表达水平最高。微囊藻毒素处理后,CpMafK mRNA 在血细胞和肝胰腺中的表达水平上调。CpMafK cDNA 被克隆到质粒 pET-32 中,重组蛋白在大肠杆菌 BL21(DE3)中表达。CpMafK 可以在体外与 CpGST1 和 CpGST2 的启动子高亲和力结合。因此,CpMafK 可以调节解毒相关基因的表达。