Bossus Maryline C, Madsen Steffen S, Tipsmark Christian K
Department of Biological Sciences, University of Arkansas, SCEN 601, Fayetteville, AR 72701, USA.
Department of Biological Sciences, University of Arkansas, SCEN 601, Fayetteville, AR 72701, USA; Department of Biology, University of Southern Denmark, Campusvej 55, 5230 Odense M, Denmark.
Comp Biochem Physiol A Mol Integr Physiol. 2015 Sep;187:74-85. doi: 10.1016/j.cbpa.2015.04.017. Epub 2015 May 7.
Salinity regulation of 13 claudin paralogs was investigated in osmoregulatory organs of euryhaline Japanese medaka. They were identified by blast-search in the medaka genome database based on representation in osmoregulatory organs of other teleosts. Our hypothesis was that, because of their sequence similarities to mammalian orthologs previously characterized as barrier- and ion-selective channel-forming proteins, these paralogs would respond to salinity according to expected modulation of osmoregulatory function. Cldn10c, -10d, -10e, -10f, -27a, -28a, -28b and -30c had 4- to 100-fold higher expression in gill than other examined organs. Two splice variants of cldn10b were predominantly expressed in kidney, while cldn15a, -15b and -25 were found mainly in intestine. In gills, cldn27a, -28a, -28b and -30c did not change between fresh water (FW) and seawater (SW)-acclimated fish, while cldn10c, -10d, -10e, and -10f were most abundant in SW. Short-term SW transfer induced up-regulation of cldn10 gill paralogs after 1 day, decrease in cldn28b and no difference for cldn27a, -28a and -30c. The reverse pattern was observed after FW transfer of SW medaka. Intestinal cldn15a and -25 did not differ between FW and SW fish. However, cldn15b was 10-fold higher in FW than SW, suggesting a role in functional modulation of the intestine related to water and salt transport. In kidney, cldn10bs were elevated in SW fish, suggesting a role in paracellular ion transport in the marine nephron. Based on in silico analysis, most gill Cldn10s were predicted to form cation pores, whereas Cldn27a, 28a, 28b and 30c may increase epithelial resistance.
在广盐性日本青鳉的渗透调节器官中研究了13种紧密连接蛋白旁系同源物的盐度调节。它们是通过在青鳉基因组数据库中进行blast搜索,基于其他硬骨鱼的渗透调节器官中的表达情况来鉴定的。我们的假设是,由于它们与先前被表征为屏障和离子选择性通道形成蛋白的哺乳动物直系同源物具有序列相似性,这些旁系同源物将根据渗透调节功能的预期调节对盐度作出反应。紧密连接蛋白10c、-10d、-10e、-10f、-27a、-28a、-28b和-30c在鳃中的表达比其他检测器官高4至100倍。紧密连接蛋白10b的两种剪接变体主要在肾脏中表达,而紧密连接蛋白15a、-15b和-25主要在肠道中发现。在鳃中,紧密连接蛋白27a、-28a、-28b和-30c在淡水(FW)和海水(SW)适应的鱼之间没有变化,而紧密连接蛋白10c、-10d、-10e和-10f在SW中最为丰富。短期SW转移在1天后诱导鳃紧密连接蛋白10旁系同源物上调,紧密连接蛋白2(8)b减少,紧密连接蛋白27a、-28a和-30c无差异。在SW青鳉进行FW转移后观察到相反的模式。肠道紧密连接蛋白15a和-(25)在FW和SW鱼之间没有差异。然而,紧密连接蛋白15b在FW中比SW高10倍,表明其在与水和盐运输相关的肠道功能调节中起作用。在肾脏中,紧密连接蛋白10b在SW鱼中升高,表明其在海洋肾单位的细胞旁离子转运中起作用。基于计算机分析,大多数鳃紧密连接蛋白10预计形成阳离子孔,而紧密连接蛋白27a、28a、28b和30c可能增加上皮抗性。