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Parasitic plants have increased rates of molecular evolution across all three genomes

Bromham, Lindell; Cowman, Peter F; Lanfear, Robert

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BACKGROUND Theoretical models and experimental evidence suggest that rates of molecular evolution could be raised in parasitic organisms compared to non-parasitic taxa. Parasitic plants provide an ideal test for these predictions, as there are at least a dozen independent origins of the parasitic lifestyle in angiosperms. Studies of a number of parasitic plant lineages have suggested faster rates of molecular evolution, but the results of some studies have been mixed. Comparative analysis of...[Show more]

dc.contributor.authorBromham, Lindell
dc.contributor.authorCowman, Peter F
dc.contributor.authorLanfear, Robert
dc.date.accessioned2015-12-03T00:22:11Z
dc.date.available2015-12-03T00:22:11Z
dc.identifier.issn1471-2148
dc.identifier.urihttp://hdl.handle.net/1885/16986
dc.description.abstractBACKGROUND Theoretical models and experimental evidence suggest that rates of molecular evolution could be raised in parasitic organisms compared to non-parasitic taxa. Parasitic plants provide an ideal test for these predictions, as there are at least a dozen independent origins of the parasitic lifestyle in angiosperms. Studies of a number of parasitic plant lineages have suggested faster rates of molecular evolution, but the results of some studies have been mixed. Comparative analysis of all parasitic plant lineages, including sequences from all three genomes, is needed to examine the generality of the relationship between rates of molecular evolution and parasitism in plants. RESULTS We analysed DNA sequence data from the mitochondrial, nuclear and chloroplast genomes for 12 independent evolutionary origins of parasitism in angiosperms. We demonstrated that parasitic lineages have a faster rate of molecular evolution than their non-parasitic relatives in sequences for all three genomes, for both synonymous and nonsynonymous substitutions. CONCLUSIONS Our results prove that raised rates of molecular evolution are a general feature of parasitic plants, not confined to a few taxa or specific genes. We discuss possible causes for this relationship, including increased positive selection associated with host-parasite arms races, relaxed selection, reduced population size or repeated bottlenecks, increased mutation rates, and indirect causal links with generation time and body size. We find no evidence that faster rates are due to smaller effective populations sizes or changes in selection pressure. Instead, our results suggest that parasitic plants have a higher mutation rate than their close non-parasitic relatives. This may be due to a direct connection, where some aspect of the parasitic lifestyle drives the evolution of raised mutation rates. Alternatively, this pattern may be driven by an indirect connection between rates and parasitism: for example, parasitic plants tend to be smaller than their non-parasitic relatives, which may result in more cell generations per year, thus a higher rate of mutations arising from DNA copy errors per unit time. Demonstration that adoption of a parasitic lifestyle influences the rate of genomic evolution is relevant to attempts to infer molecular phylogenies of parasitic plants and to estimate their evolutionary divergence times using sequence data.
dc.publisherBioMed Central
dc.rights© 2013 Bromham et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.sourceBMC Evolutionary Biology
dc.source.urihttp://www.biomedcentral.com/1471-2148/13/126
dc.subjectangiosperms
dc.subjectcell nucleus
dc.subjectmutation rate
dc.subjectphylogeny
dc.subjectplant weeds
dc.subjectselection, genetic
dc.subjectevolution, molecular
dc.subjectgenome, chloroplast
dc.subjectgenome, mitochondrial
dc.subjectgenome, plant
dc.titleParasitic plants have increased rates of molecular evolution across all three genomes
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume13
dc.date.issued2013-06-19
local.identifier.absfor060399
local.identifier.ariespublicationu9511635xPUB1130
local.publisher.urlhttp://www.biomedcentral.com/
local.type.statusPublished Version
local.contributor.affiliationBromham, Lindell, College of Medicine, Biology and Environment, CMBE Research School of Biology, Division of Evolution, Ecology & Genetics, The Australian National University
local.contributor.affiliationCowman, Peter, College of Medicine, Biology and Environment, CMBE Research School of Biology, Division of Evolution, Ecology & Genetics, The Australian National University
local.contributor.affiliationLanfear, Robert, College of Medicine, Biology and Environment, CMBE Research School of Biology, Division of Evolution, Ecology & Genetics, The Australian National University
local.identifier.essn1471-2148
local.bibliographicCitation.issue1
local.bibliographicCitation.startpage126
local.bibliographicCitation.lastpage11
local.identifier.doi10.1186/1471-2148-13-126
local.identifier.absseo970106
dc.date.updated2015-12-10T10:06:12Z
local.identifier.scopusID2-s2.0-84879052543
local.identifier.thomsonID000321015100001
CollectionsANU Research Publications

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