Long- and Short-Term Selective Forces on Malaria Parasite Genomes
Plasmodium parasites, the causal agents of malaria, result in more than 1 million deaths annually. Plasmodium are unicellular eukaryotes with small ∼23 Mb genomes encoding ∼5200 protein-coding genes. The protein-coding genes comprise about half of these genomes. Although evolutionary processes have...
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Published in | PLoS genetics Vol. 6; no. 9; p. e1001099 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
01.09.2010
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
ISSN | 1553-7404 1553-7390 1553-7404 |
DOI | 10.1371/journal.pgen.1001099 |
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Summary: | Plasmodium parasites, the causal agents of malaria, result in more than 1 million deaths annually. Plasmodium are unicellular eukaryotes with small ∼23 Mb genomes encoding ∼5200 protein-coding genes. The protein-coding genes comprise about half of these genomes. Although evolutionary processes have a significant impact on malaria control, the selective pressures within Plasmodium genomes are poorly understood, particularly in the non-protein-coding portion of the genome. We use evolutionary methods to describe selective processes in both the coding and non-coding regions of these genomes. Based on genome alignments of seven Plasmodium species, we show that protein-coding, intergenic and intronic regions are all subject to purifying selection and we identify 670 conserved non-genic elements. We then use genome-wide polymorphism data from P. falciparum to describe short-term selective processes in this species and identify some candidate genes for balancing (diversifying) selection. Our analyses suggest that there are many functional elements in the non-genic regions of these genomes and that adaptive evolution has occurred more frequently in the protein-coding regions of the genome. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Conceived and designed the experiments: ETD DCJ. Performed the experiments: SN AB GM DCJ. Analyzed the data: SN SvD PPG TDO JM ETD DCJ. Contributed reagents/materials/analysis tools: AK TDO AP MB JM DCJ. Wrote the paper: SN ETD DCJ. Identified and characterized CEs, ran SISSIz, identified SNPs, conducted polymorphism analysis, collated analysis: DCJ. Conducted divergence and constraint analysis, integrated genome annotations and alignments, ran RNAz: SN. Created alignments: AB JM. Obtained and mapped P. falciparum reads to the reference: GM. Assisted with RNA-Seq transcriptome analysis: TDO. Contributed suggestions for analysis: AP MB. Initiated the study, assisted with data analysis: ETD. |
ISSN: | 1553-7404 1553-7390 1553-7404 |
DOI: | 10.1371/journal.pgen.1001099 |