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Evolution of the rapidly mutating human salivary agglutinin gene (DMBT1) and population subsistence strategy.

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posted on 2015-05-01, 14:12 authored by Shamik Polley, S. Louzada, D. Forni, M. Sironi, Theodosius Balaskas, D. S. Hains, F. Yang, Edward J. Hollox
The dietary change resulting from the domestication of plant and animal species and development of agriculture at different locations across the world was one of the most significant changes in human evolution. An increase in dietary carbohydrates caused an increase in dental caries following the development of agriculture, mediated by the cariogenic oral bacterium Streptococcus mutans. Salivary agglutinin [SAG, encoded by the deleted in malignant brain tumors 1 (DMBT1) gene] is an innate immune receptor glycoprotein that binds a variety of bacteria and viruses, and mediates attachment of S. mutans to hydroxyapatite on the surface of the tooth. In this study we show that multiallelic copy number variation (CNV) within DMBT1 is extensive across all populations and is predicted to result in between 7-20 scavenger-receptor cysteine-rich (SRCR) domains within each SAG molecule. Direct observation of de novo mutation in multigeneration families suggests these CNVs have a very high mutation rate for a protein-coding locus, with a mutation rate of up to 5% per gamete. Given that the SRCR domains bind S. mutans and hydroxyapatite in the tooth, we investigated the association of sequence diversity at the SAG-binding gene of S. mutans, and DMBT1 CNV. Furthermore, we show that DMBT1 CNV is also associated with a history of agriculture across global populations, suggesting that dietary change as a result of agriculture has shaped the pattern of CNV at DMBT1, and that the DMBT1-S. mutans interaction is a promising model of host-pathogen-culture coevolution in humans.

Funding

This work was funded by a Government of India Ministry of Social Justice and Empowerment PhD studentship (to S.P. and E.J.H.). E.J.H. was supported in part by a Medical Research Council New Investigator Grant (GO801123). S.L. and F.Y. were supported by the Wellcome Trust (WT098051). D.S.H. was supported by NIH Grant RC4DK090937-01. This research used the ALICE and SPECTRE High Performance Computing Facilities at the University of Leicester.

History

Citation

Proceedings of the National Academy of Sciences of U.S.A. 2015, 112 (16), pp. 5105-5110

Author affiliation

/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY/School of Biological Sciences/Department of Genetics

Version

  • AM (Accepted Manuscript)

Published in

Proceedings of the National Academy of Sciences of U.S.A. 2015

Publisher

National Academy of Sciences

eissn

1091-6490

Copyright date

5105

Available date

2015-05-01

Publisher version

http://www.pnas.org/content/112/16/5105

Notes

This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1416531112/-/DCSupplemental.

Language

en

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