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Single-Nucleotide Polymorphisms and Genome Diversity in Plasmodium vivax
The study of genetic variation in malaria parasites has practical significance for developing strategies to control the disease. Vaccines based on highly polymorphic antigens may be confounded by allelic restriction of the host immune response. In response to drug pressure, a highly plastic genome m...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2003-07, Vol.100 (14), p.8502-8507 |
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creator | Feng, Xiaorong Carlton, Jane M. Joy, Deirdre A. Mu, Jianbing Furuya, Tetsuya Suh, Bernard B. Wang, Yufeng Barnwell, John W. Su, Xin-Zhuan |
description | The study of genetic variation in malaria parasites has practical significance for developing strategies to control the disease. Vaccines based on highly polymorphic antigens may be confounded by allelic restriction of the host immune response. In response to drug pressure, a highly plastic genome may generate resistant mutants more easily than a monomorphic one. Additionally, the study of the distribution of genomic polymorphisms may provide information leading to the identification of genes associated with traits such as parasite development and drug resistance. Indeed, the age and diversity of the human malaria parasite Plasmodium falciparum has been the subject of recent debate, because an ancient parasite with a complex genome is expected to present greater challenges for drug and vaccine development. The genome diversity of the important human pathogen Plasmodium vivax, however, remains essentially unknown. Here we analyze an ≈100-kb contiguous chromosome segment from five isolates, revealing 191 single-nucleotide polymorphisms (SNPs) and 44 size polymorphisms. The SNPs are not evenly distributed across the segment with blocks of high and low diversity. Whereas the majority (≈63%) of the SNPs are in intergenic regions, introns contain significantly less SNPs than intergenic sequences. Polymorphic tandem repeats are abundant and are more uniformly distributed at a frequency of about one polymorphic tandem repeat per 3 kb. These data show that P. vivax has a highly diverse genome, and provide useful information for further understanding the genome diversity of the parasite. |
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Vaccines based on highly polymorphic antigens may be confounded by allelic restriction of the host immune response. In response to drug pressure, a highly plastic genome may generate resistant mutants more easily than a monomorphic one. Additionally, the study of the distribution of genomic polymorphisms may provide information leading to the identification of genes associated with traits such as parasite development and drug resistance. Indeed, the age and diversity of the human malaria parasite Plasmodium falciparum has been the subject of recent debate, because an ancient parasite with a complex genome is expected to present greater challenges for drug and vaccine development. The genome diversity of the important human pathogen Plasmodium vivax, however, remains essentially unknown. Here we analyze an ≈100-kb contiguous chromosome segment from five isolates, revealing 191 single-nucleotide polymorphisms (SNPs) and 44 size polymorphisms. The SNPs are not evenly distributed across the segment with blocks of high and low diversity. Whereas the majority (≈63%) of the SNPs are in intergenic regions, introns contain significantly less SNPs than intergenic sequences. Polymorphic tandem repeats are abundant and are more uniformly distributed at a frequency of about one polymorphic tandem repeat per 3 kb. These data show that P. vivax has a highly diverse genome, and provide useful information for further understanding the genome diversity of the parasite.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1232502100</identifier><identifier>PMID: 12799466</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Animals ; Biological Sciences ; Chromosome Mapping ; Chromosomes ; DNA ; DNA, Protozoan - genetics ; Genes ; Genes, Protozoan ; Genetic polymorphism ; Genetic Variation ; Genome, Protozoan ; Genomes ; Genomics ; Haplotypes - genetics ; Intergenic DNA ; Introns ; Introns - genetics ; Molecular Sequence Data ; Nucleotides ; Parasites ; Parasitism ; Plasma ; Plasmodium falciparum - genetics ; Plasmodium vivax - genetics ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide ; Protozoan Proteins - genetics ; Sequence Alignment ; Sequence Analysis, DNA ; Species Specificity ; Tandem Repeat Sequences</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2003-07, Vol.100 (14), p.8502-8507</ispartof><rights>Copyright 1993-2003 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Jul 8, 2003</rights><rights>Copyright © 2003, The National Academy of Sciences 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-20b73234090d92f0ec066d90a3fe4b11f1a49786e92ce1e7d803e2c7ad4c7e523</citedby><cites>FETCH-LOGICAL-c524t-20b73234090d92f0ec066d90a3fe4b11f1a49786e92ce1e7d803e2c7ad4c7e523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/100/14.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3139956$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3139956$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12799466$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Xiaorong</creatorcontrib><creatorcontrib>Carlton, Jane M.</creatorcontrib><creatorcontrib>Joy, Deirdre A.</creatorcontrib><creatorcontrib>Mu, Jianbing</creatorcontrib><creatorcontrib>Furuya, Tetsuya</creatorcontrib><creatorcontrib>Suh, Bernard B.</creatorcontrib><creatorcontrib>Wang, Yufeng</creatorcontrib><creatorcontrib>Barnwell, John W.</creatorcontrib><creatorcontrib>Su, Xin-Zhuan</creatorcontrib><title>Single-Nucleotide Polymorphisms and Genome Diversity in Plasmodium vivax</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>The study of genetic variation in malaria parasites has practical significance for developing strategies to control the disease. 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The SNPs are not evenly distributed across the segment with blocks of high and low diversity. Whereas the majority (≈63%) of the SNPs are in intergenic regions, introns contain significantly less SNPs than intergenic sequences. Polymorphic tandem repeats are abundant and are more uniformly distributed at a frequency of about one polymorphic tandem repeat per 3 kb. 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Vaccines based on highly polymorphic antigens may be confounded by allelic restriction of the host immune response. In response to drug pressure, a highly plastic genome may generate resistant mutants more easily than a monomorphic one. Additionally, the study of the distribution of genomic polymorphisms may provide information leading to the identification of genes associated with traits such as parasite development and drug resistance. Indeed, the age and diversity of the human malaria parasite Plasmodium falciparum has been the subject of recent debate, because an ancient parasite with a complex genome is expected to present greater challenges for drug and vaccine development. The genome diversity of the important human pathogen Plasmodium vivax, however, remains essentially unknown. Here we analyze an ≈100-kb contiguous chromosome segment from five isolates, revealing 191 single-nucleotide polymorphisms (SNPs) and 44 size polymorphisms. The SNPs are not evenly distributed across the segment with blocks of high and low diversity. Whereas the majority (≈63%) of the SNPs are in intergenic regions, introns contain significantly less SNPs than intergenic sequences. Polymorphic tandem repeats are abundant and are more uniformly distributed at a frequency of about one polymorphic tandem repeat per 3 kb. These data show that P. vivax has a highly diverse genome, and provide useful information for further understanding the genome diversity of the parasite.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>12799466</pmid><doi>10.1073/pnas.1232502100</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological Sciences Chromosome Mapping Chromosomes DNA DNA, Protozoan - genetics Genes Genes, Protozoan Genetic polymorphism Genetic Variation Genome, Protozoan Genomes Genomics Haplotypes - genetics Intergenic DNA Introns Introns - genetics Molecular Sequence Data Nucleotides Parasites Parasitism Plasma Plasmodium falciparum - genetics Plasmodium vivax - genetics Polymerase Chain Reaction Polymorphism, Single Nucleotide Protozoan Proteins - genetics Sequence Alignment Sequence Analysis, DNA Species Specificity Tandem Repeat Sequences |
title | Single-Nucleotide Polymorphisms and Genome Diversity in Plasmodium vivax |
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