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Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland
PURPOSE: Salivary fluid formation is primarily driven by Ca(2+)-activated, apical efflux of chloride into the lumen of the salivary acinus. The anoctamin1 protein is an anion channel with properties resembling the endogenous calcium-activated chloride channels. In order to better understand the role...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Periodontology
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415004/ https://www.ncbi.nlm.nih.gov/pubmed/25932341 http://dx.doi.org/10.5051/jpis.2015.45.2.69 |
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author | Han, Ji-hye Kim, Hye-mi Seo, Deog-Gyu Lee, Gene Jeung, Eui-Bae Yu, Frank H. |
author_facet | Han, Ji-hye Kim, Hye-mi Seo, Deog-Gyu Lee, Gene Jeung, Eui-Bae Yu, Frank H. |
author_sort | Han, Ji-hye |
collection | PubMed |
description | PURPOSE: Salivary fluid formation is primarily driven by Ca(2+)-activated, apical efflux of chloride into the lumen of the salivary acinus. The anoctamin1 protein is an anion channel with properties resembling the endogenous calcium-activated chloride channels. In order to better understand the role of anoctamin proteins in salivary exocrine secretion, the expression of the ten members of the anoctamin gene family in the mouse submandibular gland was studied. METHODS: Total RNA extracted from mouse submandibular salivary glands was reverse transcribed using primer pairs to amplify the full-length coding regions of each anoctamin gene and was subcloned into plasmid vectors for DNA sequencing. Alternative splice variants were also screened by polymerase chain reaction using primer pairs that amplified six overlapping regions of the complementary DNA of each anoctamin gene, spanning multiple exons. RESULTS: Multiple anoctamin transcripts were found in the mouse submandibular salivary gland, including full-length transcripts of anoctamin1, anoctamin3, anoctamin4, anoctamin5, anoctamin6, anoctamin9, and anoctamin10. Exon-skipping splicing in the N-terminal exons of the anoctamins1, anoctamin5, and anoctamin6 genes resulted in multiple alternative splice variants. No expression of anoctamin2, anoctamin7, or anoctamin8 was found. CONCLUSIONS: The predominant anoctamin transcript expressed in the mouse submandibular gland is anoctamin1ac. The chloride channel protein produced by anoctamin1ac is likely responsible for the Ca(2+)-activated chloride efflux, which is the rate-limiting step in salivary exocrine secretion. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-4415004 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Korean Academy of Periodontology |
record_format | MEDLINE/PubMed |
spelling | pubmed-44150042015-04-30 Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland Han, Ji-hye Kim, Hye-mi Seo, Deog-Gyu Lee, Gene Jeung, Eui-Bae Yu, Frank H. J Periodontal Implant Sci Research Article PURPOSE: Salivary fluid formation is primarily driven by Ca(2+)-activated, apical efflux of chloride into the lumen of the salivary acinus. The anoctamin1 protein is an anion channel with properties resembling the endogenous calcium-activated chloride channels. In order to better understand the role of anoctamin proteins in salivary exocrine secretion, the expression of the ten members of the anoctamin gene family in the mouse submandibular gland was studied. METHODS: Total RNA extracted from mouse submandibular salivary glands was reverse transcribed using primer pairs to amplify the full-length coding regions of each anoctamin gene and was subcloned into plasmid vectors for DNA sequencing. Alternative splice variants were also screened by polymerase chain reaction using primer pairs that amplified six overlapping regions of the complementary DNA of each anoctamin gene, spanning multiple exons. RESULTS: Multiple anoctamin transcripts were found in the mouse submandibular salivary gland, including full-length transcripts of anoctamin1, anoctamin3, anoctamin4, anoctamin5, anoctamin6, anoctamin9, and anoctamin10. Exon-skipping splicing in the N-terminal exons of the anoctamins1, anoctamin5, and anoctamin6 genes resulted in multiple alternative splice variants. No expression of anoctamin2, anoctamin7, or anoctamin8 was found. CONCLUSIONS: The predominant anoctamin transcript expressed in the mouse submandibular gland is anoctamin1ac. The chloride channel protein produced by anoctamin1ac is likely responsible for the Ca(2+)-activated chloride efflux, which is the rate-limiting step in salivary exocrine secretion. GRAPHICAL ABSTRACT: [Image: see text] Korean Academy of Periodontology 2015-04 2015-04-29 /pmc/articles/PMC4415004/ /pubmed/25932341 http://dx.doi.org/10.5051/jpis.2015.45.2.69 Text en Copyright © 2015 Korean Academy of Periodontology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/). |
spellingShingle | Research Article Han, Ji-hye Kim, Hye-mi Seo, Deog-Gyu Lee, Gene Jeung, Eui-Bae Yu, Frank H. Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
title | Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
title_full | Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
title_fullStr | Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
title_full_unstemmed | Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
title_short | Multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
title_sort | multiple transcripts of anoctamin genes expressed in the mouse submandibular salivary gland |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415004/ https://www.ncbi.nlm.nih.gov/pubmed/25932341 http://dx.doi.org/10.5051/jpis.2015.45.2.69 |
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