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Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney

BACKGROUND: 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. RESULTS: CA-VI was located in the epith...

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Autores principales: Nishita, Toshiho, Yatsu, Juro, Murakami, Masaru, Kamoshida, Shino, Orito, Kensuke, Ichihara, Nobutune, Arishima, Kazuyoshi, Ochiai, Hideharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975938/
https://www.ncbi.nlm.nih.gov/pubmed/24576305
http://dx.doi.org/10.1186/1756-0500-7-116
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author Nishita, Toshiho
Yatsu, Juro
Murakami, Masaru
Kamoshida, Shino
Orito, Kensuke
Ichihara, Nobutune
Arishima, Kazuyoshi
Ochiai, Hideharu
author_facet Nishita, Toshiho
Yatsu, Juro
Murakami, Masaru
Kamoshida, Shino
Orito, Kensuke
Ichihara, Nobutune
Arishima, Kazuyoshi
Ochiai, Hideharu
author_sort Nishita, Toshiho
collection PubMed
description BACKGROUND: 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. RESULTS: 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). CONCLUSIONS: The localisation of CA-VI indicates that it may play a specialised role in the kidney.
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spelling pubmed-39759382014-04-05 Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney Nishita, Toshiho Yatsu, Juro Murakami, Masaru Kamoshida, Shino Orito, Kensuke Ichihara, Nobutune Arishima, Kazuyoshi Ochiai, Hideharu BMC Res Notes Research Article BACKGROUND: 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. RESULTS: 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). CONCLUSIONS: The localisation of CA-VI indicates that it may play a specialised role in the kidney. BioMed Central 2014-02-28 /pmc/articles/PMC3975938/ /pubmed/24576305 http://dx.doi.org/10.1186/1756-0500-7-116 Text en Copyright © 2014 Nishita et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Nishita, Toshiho
Yatsu, Juro
Murakami, Masaru
Kamoshida, Shino
Orito, Kensuke
Ichihara, Nobutune
Arishima, Kazuyoshi
Ochiai, Hideharu
Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney
title Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney
title_full Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney
title_fullStr Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney
title_full_unstemmed Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney
title_short Isolation and sequencing of swine carbonic anhydrase VI, an enzyme expressed in the swine kidney
title_sort isolation and sequencing of swine carbonic anhydrase vi, an enzyme expressed in the swine kidney
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975938/
https://www.ncbi.nlm.nih.gov/pubmed/24576305
http://dx.doi.org/10.1186/1756-0500-7-116
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