Authors' Affiliations
(1)
School of Life Sciences, University of Nottingham
Noble RE. Salivary alpha-amylase and lysozyme levels: a non-invasive technique for measuring parotid vs submandibular/sublingual gland activity. J Oral Science. 2000;42:83-6.Google Scholar
Granger DA, Kivlighan KT, El-Sheikh M, Gordis EB, Stroud LR. Salivary ?-amylase in biobehavioral research. Ann N Y Acad Sci. 2007;1098:122-44.Google Scholar
Nater UM, Hoppmann CA, Scott SB. Diurnal profiles of salivary cortisol and alpha-amylase change across the adult lifespan: evidence from repeated daily life assessments. Psychoneuroendocrinology. 2013;38:3167-71.Google Scholar
Lawrence HP. Salivary markers of systemic disease: noninvasive diagnosis of disease and monitoring of general health. J Canadian Dental Association. 2002;68:170-4.Google Scholar
Bank RA, Hettema EH, Muijs MA, Pals G, Arwert F, Boomsma DI, Pronk JC. Variation in gene copy number and polymorphism of the human salivary amylase isoenzyme system in Caucasians. Hum Genet. 1992;89:213-22.Google Scholar
Mandel AL, Peyrot des Gachons C, Plank KL, Alarcon S, Breslin PAS. Individual differences in AMY1 gene copy number, salivary ?-amylase levels, and the perception of oral starch. PLoS One. 2010;5:e13352.Google Scholar
Perry GH, Dominy NJ, Claw KG, Lee AS, Fiegler H, Redon R, et al. Diet and the evolution of human amylase gene copy number variation. Nat Genet. 2007;39:1256-60.Google Scholar
Pronk JC, Frants RR, Jansen W, Eriksson AW, Tonino GJM. Evidence for duplication of the human salivary amylase gene. Hum Genet. 1982;60:32-5.Google Scholar
Sudmant PH, Kitzman JO, Antonacci F, Alkan C, Malig M, Tsalenko A, et al. Diversity of human copy number variation and multicopy genes. Science. 2010;330:641-6.Google Scholar
Carpenter D, Dhar S, Mitchell L, Fu B, Tyson J, Shwan N, et al. Obesity, starch digestion and amylase: association between copy number variants at human salivary (AMY1) and pancreatic (AMY2) amylase genes. Hum Mol Genet. 2015;24:3472-80.Google Scholar
Falchi M, El-Sayed Moustafa JS, Takousis P, Pesce F, Bonnefond A, Andersson-Assarsson JC, et al. Low copy number of the salivary amylase gene predisposes to obesity. Nat Genet. 2014;46:492-7.Google Scholar
Usher CL, Handsaker RE, Esko T, Tuke MA, Weedon MN, Hastie AR, et al. Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity. Nat Genet. 2015;47:921-5.Google Scholar
Groot PC, Bleeker MJ, Pronk JC, Arwert F, Mager WH, Planta RJ, et al. The human ?-amylase multigene family consists of haplotypes with variable numbers of genes. Genomics. 1989;5:29-42.Google Scholar
Groot PC, Mager WH, Frants RR. Interpretation of polymorphic DNA patterns in the human ?-amylase multigene family. Genomics. 1991;10:779-85.Google Scholar
Groot PC, Mager WH, Henriquez NV, Pronk JC, Arwert F, Planta RJ, et al. Evolution of the human alpha-amylase multigene family through unequal, homologous, and interchromosomal and intrachromosomal crossovers. Genomics. 1990;8:97-105.Google Scholar
Yang Z-M, Lin J, Chen L-H, Zhang M, Chen W-W, Yang X-R. The roles of AMY1 copies and protein expression in human salivary ?-amylase activity. Physiol Behav. 2015;138:173-8.Google Scholar
Iontcheva I, Oppenheim FG, Troxler RF. Human salivary mucin MG1 selectively forms heterotypic complexes with amylase, proline-rich proteins, statherin, and histatins. J Dent Res. 1997;76:734-43.Google Scholar
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Copyright BioMed Central 2017
Abstract
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.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer