Nishita Toshiho, Yatsu Juro, Murakami Masaru, Kamoshida Shino, Orito Kensuke, Ichihara Nobutune, Arishima Kazuyoshi, Ochiai Hideharu
Laboratory of Physiology I, School of Veterinary Medicine, Azabu University, 1-17-71 Fuchinobe, Sagamihara, Kanagawa 252-5201, Japan.
BMC Res Notes. 2014 Feb 28;7:116. doi: 10.1186/1756-0500-7-116.
Carbonic anhydrase VI (CA-VI) is produced by the salivary gland and is secreted into the saliva. Although CA-VI is found in the epithelial cells of distal straight tubule of swine kidneys, the exact function of CA-VI in the kidneys remains unclear.
CA-VI was located in the epithelial cells of distal straight tubule of swine kidneys.A full-length cDNA clone of CA-VI was generated from the swine parotid gland by reverse transcription polymerase chain reaction, using degenerate primers designed based on conserved regions of the same locus in human and bovine tissues. The cDNA sequence was 1348 base pairs long and was predicted to encode a 317 amino acid polypeptide with a putative signal peptide of 17 amino acids. The deduced amino acid sequence of mature CA-VI was most similar (77.4%) to that of human CA-VI. CA-VI expression was confirmed in both normal and nephritic kidneys, as well as parotid. As the primers used in this study spanned two exons, the influence of genomic DNA was not detected. The expression of CA-VI was demonstrated in both normal and nephritic kidneys, and mRNA of CA-VI in the normal kidneys which was the normalised to an endogenous β-actin was 0.098 ± 0.047, while it was significantly lower in the diseased kidneys (0.012 ± 0.007). The level of CA-VI mRNA in normal kidneys was 19-fold lower than that of the parotid gland (1.887).
The localisation of CA-VI indicates that it may play a specialised role in the kidney.
碳酸酐酶VI(CA-VI)由唾液腺产生并分泌到唾液中。虽然在猪肾远直小管的上皮细胞中发现了CA-VI,但其在肾脏中的具体功能仍不清楚。
CA-VI定位于猪肾远直小管的上皮细胞中。利用基于人和牛组织中同一位点保守区域设计的简并引物,通过逆转录聚合酶链反应从猪腮腺中获得了CA-VI的全长cDNA克隆。该cDNA序列长1348个碱基对,预计编码一个317个氨基酸的多肽,带有一个17个氨基酸的假定信号肽。推导的成熟CA-VI氨基酸序列与人类CA-VI的序列最相似(77.4%)。在正常肾、肾炎肾以及腮腺中均证实了CA-VI的表达。由于本研究中使用的引物跨越两个外显子,未检测到基因组DNA的影响。在正常肾和肾炎肾中均证实了CA-VI的表达,正常肾中CA-VI的mRNA以内源性β-肌动蛋白标准化后为0.098±0.047,而在患病肾中显著降低(0.012±0.007)。正常肾中CA-VI mRNA的水平比腮腺低19倍(1.887)。
CA-VI的定位表明它可能在肾脏中发挥特殊作用。