首页> 外文OA文献 >Ontogeny of osmoregulation in the Pacific blue shrimp, Litopenaeus stylirostris (decapoda, penaeidae): Deciphering the role of the Na+/K+-ATPase
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Ontogeny of osmoregulation in the Pacific blue shrimp, Litopenaeus stylirostris (decapoda, penaeidae): Deciphering the role of the Na+/K+-ATPase

机译:太平洋蓝虾(Litopenaeus stylirostris(decapoda,penaeidae))渗透调节的发生:解读Na + / K + -aTpase的作用

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摘要

The role of the main ion transporting enzyme Na +/K + − ATPase in osmoregulation processes was investigated in Litopenaeus stylirostris. The development and localization of the osmoregulation sites were studied during ontogenesis by immunodetection of Na+ K+-ATPase using monoclonal antibodies and transmission electron microscopy (TEM). Osmoregulation sites were identified as the pleurae and branchiostegites in the zoeae and mysis stages. In the subsequent post-metamorphic stages the osmoregulatory function was mainly located in the epipodites and branchiostegites and osmotic regulation was later detected in the gills. The presence of ionocytes and microvilli in these tissues confirmed their role in ionic processes. The complete open reading frame of the mRNA coding for the α-subunit of Na + K + − ATPase was characterized in L. stylirostris. The resulting 3092-bp cDNA (LsNKA) encodes a putative 1011-amino-acid protein with a predicted molecular mass of 112.3 kDa. The inferred amino acid sequence revealed that the putative protein possesses the main structural characteristics of the Na + K + − ATPase α-subunits.Quantitative RT-PCR analyses indicated that LsNKA transcripts did not significantly vary between the different developmental stages. The number of transcripts was about 2.5-fold higher in the epipodites and gills than in any other tissues tested in juveniles. A reverse genetic approach was finally implemented to study the role of LsNKA in vivo. Knock down of LsNKA expression by gene-specific dsRNA injection led to an increase of shrimp mortality following an abrupt salinity change compared to control animals. These data strongly suggest that LsNKA plays an important role in osmoregulation when the shrimp are challenged by changing salinities.
机译:在细齿对虾中研究了主要的离子转运酶Na + / K +-ATPase在渗透调节过程中的作用。通过使用单克隆抗体和透射电子显微镜(TEM)对Na + K + -ATPase进行免疫检测,研究了渗透调节位点的发育和定位。渗透调节位点被确定为动物园和蝇sis阶段的胸膜和分支骨。在随后的亚变态阶段,渗透调节功能主要位于附睾和分支雌激素中,随后在g中检测到渗透调节。这些组织中离子细胞和微绒毛的存在证实了它们在离子过程中的作用。 stylirostris中表征了编码Na + K +-ATPaseα亚基的mRNA的完整开放阅读框。所得的3092 bp cDNA(LsNKA)编码一种推测的1011氨基酸蛋白,预测分子量为112.3 kDa。推测的氨基酸序列表明,推测的蛋白质具有Na + K +-ATPaseα-亚基的主要结构特征。定量RT-PCR分析表明,LsNKA转录本在不同发育阶段之间没有显着变化。附生动物和ill中的转录物数量比在少年中测试的任何其他组织高约2.5倍。最终实施了反向遗传方法来研究LsNKA在体内的作用。与对照动物相比,通过盐特异性突变,通过基因特异性dsRNA注射抑制LsNKA表达导致虾死亡率增加。这些数据强烈表明,当虾受到盐度变化的挑战时,LsNKA在渗透调节中起着重要作用。

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