On the origins of Mendelian disease genes in man: the impact of gene duplication

Dickerson, J. E. and Robertson, D. L. (2012) On the origins of Mendelian disease genes in man: the impact of gene duplication. Molecular Biology and Evolution, 29(1), pp. 61-69. (doi: 10.1093/molbev/msr111) (PMID:21705381) (PMCID:PMC3709195)

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Over 3,000 human diseases are known to be linked to heritable genetic variation, mapping to over 1,700 unique genes. Dating of the evolutionary age of these disease-associated genes has suggested that they have a tendency to be ancient, specifically coming into existence with early metazoa. The approach taken by past studies, however, assumes that the age of a disease is the same as the age of its common ancestor, ignoring the fundamental contribution of duplication events in the evolution of new genes and function. Here, we date both the common ancestor and the duplication history of known human disease-associated genes. We find that the majority of disease genes (80%) are genes that have been duplicated in their evolutionary history. Periods for which there are more disease-associated genes, for example, at the origins of bony vertebrates, are explained by the emergence of more genes at that time, and the majority of these are duplicates inferred to have arisen by whole-genome duplication. These relationships are similar for different disease types and the disease-associated gene's cellular function. This indicates that the emergence of duplication-associated diseases has been ongoing and approximately constant (relative to the retention of duplicate genes) throughout the evolution of life. This continued until approximately 390 Ma from which time relatively fewer novel genes came into existence on the human lineage, let alone disease genes. For single-copy genes associated with disease, we find that the numbers of disease genes decreases with recency. For the majority of duplicates, the disease-associated mutation is associated with just one of the duplicate copies. A universal explanation for heritable disease is, thus, that it is merely a by-product of the evolutionary process; the evolution of new genes (de novo or by duplication) results in the potential for new diseases to emerge.

Item Type:Articles
Additional Information:J.E.D. was supported by a Wellcome Trust studentship and VIP award.
Glasgow Author(s) Enlighten ID:Robertson, Professor David and Dickerson, Dr Jonathan
Authors: Dickerson, J. E., and Robertson, D. L.
College/School:College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
College of Medical Veterinary and Life Sciences > Institute of Infection Immunity and Inflammation
Journal Name:Molecular Biology and Evolution
Journal Abbr.:Mol Biol Evol
Publisher:Oxford University Press
ISSN (Online):1537-1719
Published Online:24 June 2011
Copyright Holders:Copyright © 2011 The Authors
First Published:First published in Molecular Biology and Evolution 29(1): 61-69
Publisher Policy:Reproduced under a Creative Commons License

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