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Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity

BACKGROUND: Salivary amylase in humans is encoded by the copy variable gene AMY1 in the amylase gene cluster on chromosome 1. Although the role of salivary amylase is well established, the consequences of the copy number variation (CNV) at AMY1 on salivary amylase protein production are less well un...

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Autores principales: Carpenter, Danielle, Mitchell, Laura M., Armour, John A. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319014/
https://www.ncbi.nlm.nih.gov/pubmed/28219410
http://dx.doi.org/10.1186/s40246-017-0097-3
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author Carpenter, Danielle
Mitchell, Laura M.
Armour, John A. L.
author_facet Carpenter, Danielle
Mitchell, Laura M.
Armour, John A. L.
author_sort Carpenter, Danielle
collection PubMed
description BACKGROUND: Salivary amylase in humans is encoded by the copy variable gene AMY1 in the amylase gene cluster on chromosome 1. Although the role of salivary amylase is well established, the consequences of the copy number variation (CNV) at AMY1 on salivary amylase protein production are less well understood. The amylase gene cluster is highly structured with a fundamental difference between odd and even AMY1 copy number haplotypes. In this study, we aimed to explore, in samples from 119 unrelated individuals, not only the effects of AMY1 CNV on salivary amylase protein expression and amylase enzyme activity but also whether there is any evidence for underlying difference between the common haplotypes containing odd numbers of AMY1 and even copy number haplotypes. RESULTS: AMY1 copy number was significantly correlated with the variation observed in salivary amylase production (11.7% of variance, P < 0.0005) and enzyme activity (13.6% of variance, P < 0.0005) but did not explain the majority of observed variation between individuals. AMY1-odd and AMY1-even haplotypes showed a different relationship between copy number and expression levels, but the difference was not statistically significant (P = 0.052). CONCLUSIONS: Production of salivary amylase is correlated with AMY1 CNV, but the majority of interindividual variation comes from other sources. Long-range haplotype structure may affect expression, but this was not significant in our data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40246-017-0097-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-53190142017-02-24 Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity Carpenter, Danielle Mitchell, Laura M. Armour, John A. L. Hum Genomics Primary Research BACKGROUND: Salivary amylase in humans is encoded by the copy variable gene AMY1 in the amylase gene cluster on chromosome 1. Although the role of salivary amylase is well established, the consequences of the copy number variation (CNV) at AMY1 on salivary amylase protein production are less well understood. The amylase gene cluster is highly structured with a fundamental difference between odd and even AMY1 copy number haplotypes. In this study, we aimed to explore, in samples from 119 unrelated individuals, not only the effects of AMY1 CNV on salivary amylase protein expression and amylase enzyme activity but also whether there is any evidence for underlying difference between the common haplotypes containing odd numbers of AMY1 and even copy number haplotypes. RESULTS: AMY1 copy number was significantly correlated with the variation observed in salivary amylase production (11.7% of variance, P < 0.0005) and enzyme activity (13.6% of variance, P < 0.0005) but did not explain the majority of observed variation between individuals. AMY1-odd and AMY1-even haplotypes showed a different relationship between copy number and expression levels, but the difference was not statistically significant (P = 0.052). CONCLUSIONS: Production of salivary amylase is correlated with AMY1 CNV, but the majority of interindividual variation comes from other sources. Long-range haplotype structure may affect expression, but this was not significant in our data. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40246-017-0097-3) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-20 /pmc/articles/PMC5319014/ /pubmed/28219410 http://dx.doi.org/10.1186/s40246-017-0097-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Primary Research
Carpenter, Danielle
Mitchell, Laura M.
Armour, John A. L.
Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity
title Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity
title_full Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity
title_fullStr Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity
title_full_unstemmed Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity
title_short Copy number variation of human AMY1 is a minor contributor to variation in salivary amylase expression and activity
title_sort copy number variation of human amy1 is a minor contributor to variation in salivary amylase expression and activity
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319014/
https://www.ncbi.nlm.nih.gov/pubmed/28219410
http://dx.doi.org/10.1186/s40246-017-0097-3
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