An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi

Detalhes bibliográficos
Autor(a) principal: Martinelli, Axel
Data de Publicação: 2005
Outros Autores: Hunt, Paul, Fawcett, Richard, Cravo, Pedro V L, Walliker, David, Carter, Richard
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/117239
Resumo: BACKGROUND: Plasmodium chabaudi chabaudi can be considered as a rodent model of human malaria parasites in the genetic analysis of important characters such as drug resistance and immunity. Despite the availability of some genome sequence data, an extensive genetic linkage map is needed for mapping the genes involved in certain traits. METHODS: The inheritance of 672 Amplified Fragment Length Polymorphism (AFLP) markers from two parental clones (AS and AJ) of P. c. chabaudi was determined in 28 independent recombinant progeny clones. These, AFLP markers and 42 previously mapped Restriction Fragment Length Polymorphism (RFLP) markers (used as chromosomal anchors) were organized into linkage groups using Map Manager software. RESULTS: 614 AFLP markers formed linkage groups assigned to 10 of 14 chromosomes, and 12 other linkage groups not assigned to known chromosomes. The genetic length of the genome was estimated to be about 1676 centiMorgans (cM). The mean map unit size was estimated to be 13.7 kb/cM. This was slightly less then previous estimates for the human malaria parasite, Plasmodium falciparum CONCLUSION: The P. c. chabaudi genetic linkage map presented here is the most extensive and highly resolved so far available for this species. It can be used in conjunction with the genome databases of P. c chabaudi, P. falciparum and Plasmodium yoelii to identify genes underlying important phenotypes such as drug resistance and strain-specific immunity.
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spelling An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudiAllelesAnimalsChloroquineChromosome MappingChromosomesDNA, ProtozoanDisease Models, AnimalFemaleGenetic LinkageGenetic MarkersMalariaMiceMice, Inbred CBAMutationPlasmodium chabaudiPolymorphism, Restriction Fragment LengthRecombination, GeneticStatistics as TopicJournal ArticleResearch Support, Non-U.S. Gov'tGeneticsParasitologySDG 3 - Good Health and Well-beingBACKGROUND: Plasmodium chabaudi chabaudi can be considered as a rodent model of human malaria parasites in the genetic analysis of important characters such as drug resistance and immunity. Despite the availability of some genome sequence data, an extensive genetic linkage map is needed for mapping the genes involved in certain traits. METHODS: The inheritance of 672 Amplified Fragment Length Polymorphism (AFLP) markers from two parental clones (AS and AJ) of P. c. chabaudi was determined in 28 independent recombinant progeny clones. These, AFLP markers and 42 previously mapped Restriction Fragment Length Polymorphism (RFLP) markers (used as chromosomal anchors) were organized into linkage groups using Map Manager software. RESULTS: 614 AFLP markers formed linkage groups assigned to 10 of 14 chromosomes, and 12 other linkage groups not assigned to known chromosomes. The genetic length of the genome was estimated to be about 1676 centiMorgans (cM). The mean map unit size was estimated to be 13.7 kb/cM. This was slightly less then previous estimates for the human malaria parasite, Plasmodium falciparum CONCLUSION: The P. c. chabaudi genetic linkage map presented here is the most extensive and highly resolved so far available for this species. It can be used in conjunction with the genome databases of P. c chabaudi, P. falciparum and Plasmodium yoelii to identify genes underlying important phenotypes such as drug resistance and strain-specific immunity.Centro de Malária e outras Doenças Tropicais (CMDT)Instituto de Higiene e Medicina Tropical (IHMT)RUNMartinelli, AxelHunt, PaulFawcett, RichardCravo, Pedro V LWalliker, DavidCarter, Richard2021-05-06T22:40:45Z2005-02-112005-02-11T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article11application/pdfhttp://hdl.handle.net/10362/117239eng1475-2875PURE: 3631657https://doi.org/10.1186/1475-2875-4-11info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T05:00:20Zoai:run.unl.pt:10362/117239Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:43:33.161085Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
title An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
spellingShingle An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
Martinelli, Axel
Alleles
Animals
Chloroquine
Chromosome Mapping
Chromosomes
DNA, Protozoan
Disease Models, Animal
Female
Genetic Linkage
Genetic Markers
Malaria
Mice
Mice, Inbred CBA
Mutation
Plasmodium chabaudi
Polymorphism, Restriction Fragment Length
Recombination, Genetic
Statistics as Topic
Journal Article
Research Support, Non-U.S. Gov't
Genetics
Parasitology
SDG 3 - Good Health and Well-being
title_short An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
title_full An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
title_fullStr An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
title_full_unstemmed An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
title_sort An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
author Martinelli, Axel
author_facet Martinelli, Axel
Hunt, Paul
Fawcett, Richard
Cravo, Pedro V L
Walliker, David
Carter, Richard
author_role author
author2 Hunt, Paul
Fawcett, Richard
Cravo, Pedro V L
Walliker, David
Carter, Richard
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Centro de Malária e outras Doenças Tropicais (CMDT)
Instituto de Higiene e Medicina Tropical (IHMT)
RUN
dc.contributor.author.fl_str_mv Martinelli, Axel
Hunt, Paul
Fawcett, Richard
Cravo, Pedro V L
Walliker, David
Carter, Richard
dc.subject.por.fl_str_mv Alleles
Animals
Chloroquine
Chromosome Mapping
Chromosomes
DNA, Protozoan
Disease Models, Animal
Female
Genetic Linkage
Genetic Markers
Malaria
Mice
Mice, Inbred CBA
Mutation
Plasmodium chabaudi
Polymorphism, Restriction Fragment Length
Recombination, Genetic
Statistics as Topic
Journal Article
Research Support, Non-U.S. Gov't
Genetics
Parasitology
SDG 3 - Good Health and Well-being
topic Alleles
Animals
Chloroquine
Chromosome Mapping
Chromosomes
DNA, Protozoan
Disease Models, Animal
Female
Genetic Linkage
Genetic Markers
Malaria
Mice
Mice, Inbred CBA
Mutation
Plasmodium chabaudi
Polymorphism, Restriction Fragment Length
Recombination, Genetic
Statistics as Topic
Journal Article
Research Support, Non-U.S. Gov't
Genetics
Parasitology
SDG 3 - Good Health and Well-being
description BACKGROUND: Plasmodium chabaudi chabaudi can be considered as a rodent model of human malaria parasites in the genetic analysis of important characters such as drug resistance and immunity. Despite the availability of some genome sequence data, an extensive genetic linkage map is needed for mapping the genes involved in certain traits. METHODS: The inheritance of 672 Amplified Fragment Length Polymorphism (AFLP) markers from two parental clones (AS and AJ) of P. c. chabaudi was determined in 28 independent recombinant progeny clones. These, AFLP markers and 42 previously mapped Restriction Fragment Length Polymorphism (RFLP) markers (used as chromosomal anchors) were organized into linkage groups using Map Manager software. RESULTS: 614 AFLP markers formed linkage groups assigned to 10 of 14 chromosomes, and 12 other linkage groups not assigned to known chromosomes. The genetic length of the genome was estimated to be about 1676 centiMorgans (cM). The mean map unit size was estimated to be 13.7 kb/cM. This was slightly less then previous estimates for the human malaria parasite, Plasmodium falciparum CONCLUSION: The P. c. chabaudi genetic linkage map presented here is the most extensive and highly resolved so far available for this species. It can be used in conjunction with the genome databases of P. c chabaudi, P. falciparum and Plasmodium yoelii to identify genes underlying important phenotypes such as drug resistance and strain-specific immunity.
publishDate 2005
dc.date.none.fl_str_mv 2005-02-11
2005-02-11T00:00:00Z
2021-05-06T22:40:45Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/117239
url http://hdl.handle.net/10362/117239
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1475-2875
PURE: 3631657
https://doi.org/10.1186/1475-2875-4-11
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 11
application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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