An AFLP-based genetic linkage map of Plasmodium chabaudi chabaudi
Autor(a) principal: | |
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Data de Publicação: | 2005 |
Outros Autores: | , , , , |
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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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) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799138044693970944 |