Islam Zinia, Hayashi Naoko, Inoue Hana, Umezawa Takahiro, Kimura Yuuri, Doi Hiroyuki, Romero Michael F, Hirose Shigehisa, Kato Akira
Department of Biological Sciences, Tokyo Institute of Technology, Yokohama, Japan;
Department of Physiology, Tokyo Medical University, Tokyo, Japan;
Am J Physiol Regul Integr Comp Physiol. 2014 Sep 1;307(5):R525-37. doi: 10.1152/ajpregu.00032.2014. Epub 2014 Jun 25.
The kidney of marine teleosts is the major site of Mg(2+) excretion and produces urine with a high Mg(2+) concentration. However, the transporters involved in Mg(2+) excretion are poorly understood. The cyclin M (Cnnm; also known as ancient conserved domain protein) family comprises membrane proteins homologous to the bacterial Mg(2+) and Co(2+) efflux protein, CorC. To understand the molecular mechanism of Mg(2+) homeostasis in marine teleosts, we analyzed the expression of the Cnnm family genes in the seawater (SW) pufferfish, torafugu (Takifugu rubripes), and the closely related euryhaline species, mefugu (Takifugu obscurus). Database mining and phylogenetic analysis indicated that the Takifugu genome contains six members of the Cnnm family: two orthologs of Cnnm1, one of Cnnm2, one of Cnnm3, and two of Cnnm4. RT-PCR analyses indicated that Cnnm2, Cnnm3, and Cnnm4a are expressed in the kidney, whereas other members are mainly expressed in the brain. Renal expression of Cnnm3 was upregulated in SW mefugu, whereas renal expression of Cnnm2 was upregulated in freshwater (FW) mefugu. No significant difference was observed in renal expression of Cnnm4a between SW and FW mefugu. In situ hybridization and immunohistochemical analyses of the SW mefugu kidney revealed that Cnnm3 is expressed in the proximal tubule, and its product localizes to the lateral membrane. When Cnnm3 was expressed in Xenopus laevis oocytes, whole cellular Mg(2+) content and free intracellular Mg(2+) activity significantly decreased. These results suggest that Cnnm3 is involved in body fluid Mg(2+) homeostasis in marine teleosts.
海洋硬骨鱼的肾脏是镁离子(Mg²⁺)排泄的主要部位,产生的尿液中镁离子浓度很高。然而,参与镁离子排泄的转运蛋白目前还知之甚少。细胞周期蛋白M(Cnnm;也称为古老保守结构域蛋白)家族由与细菌镁离子和钴离子(Co²⁺)外排蛋白CorC同源的膜蛋白组成。为了了解海洋硬骨鱼体内镁离子稳态的分子机制,我们分析了海水(SW)河豚、红鳍东方鲀(Takifugu rubripes)以及亲缘关系密切的广盐性物种、暗纹东方鲀(Takifugu obscurus)中Cnnm家族基因的表达情况。数据库挖掘和系统发育分析表明,东方鲀基因组包含Cnnm家族的六个成员:两个Cnnm1直系同源物、一个Cnnm2、一个Cnnm3和两个Cnnm4。逆转录聚合酶链反应(RT-PCR)分析表明,Cnnm2、Cnnm3和Cnnm4a在肾脏中表达,而其他成员主要在大脑中表达。在SW暗纹东方鲀中,Cnnm3的肾脏表达上调,而在淡水(FW)暗纹东方鲀中,Cnnm2的肾脏表达上调。SW和FW暗纹东方鲀之间Cnnm4a的肾脏表达未观察到显著差异。对SW暗纹东方鲀肾脏的原位杂交和免疫组织化学分析表明,Cnnm3在近端小管中表达,其产物定位于侧膜。当Cnnm3在非洲爪蟾卵母细胞中表达时,整个细胞的镁离子含量和细胞内游离镁离子活性显著降低。这些结果表明,Cnnm3参与了海洋硬骨鱼体内体液镁离子的稳态调节。