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dc.contributor.authorAmills, M.
dc.contributor.authorJiménez, N.
dc.contributor.authorVillalba, D.
dc.contributor.authorTor, M.
dc.contributor.authorMolina, E.
dc.contributor.authorCubiló, D.
dc.contributor.authorMarcos, C.
dc.contributor.authorFrancesch, A.
dc.contributor.authorSánchez, A.
dc.contributor.authorEstany, J.
dc.contributor.otherProducció Animalca
dc.date.accessioned2025-02-28T11:52:21Z
dc.date.available2025-02-28T11:52:21Z
dc.date.issued2003-10-01
dc.identifier.citationAmills, M, N Jimenez, D Villalba, M Tor, E Molina, D Cubilo, C Marcos, A Francesch, A Sanchez, and J Estany. 2003. “Identification of Three Single Nucleotide Polymorphisms in the Chicken Insulin-like Growth Factor 1 and 2 Genes and Their Associations With Growth and Feeding Traits.” Poultry Science 82 (10): 1485-1493. doi: 10.1093/ps/82.10.1485ca
dc.identifier.issn0032-5791ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/3690
dc.description.abstractThe chicken insulin-like growth factor (IGF)1 and IGF2 genes have been partially sequenced in six individuals of each of two chicken strains of the Black Penedesenca breed (PN and MN). These two strains are genetically diverse for growth traits. Sequence alignment revealed the existence of three single nucleotide polymorphisms (SNP) (IGF1-SNP1, IGF2-SNP2, and IGF2-SNP3). These three SNP and a fourth IGF1 polymorphism (IGF1- SNP4) were typed in 60 individuals from each strain by using PCR-RFLP or primer extension analysis. No significant associations among these four SNP, growth traits, and plasma IGF1 concentration were identified. In contrast, suggestive associations (P ≤ 0.05) were found between IGF1-SNP1 and average daily gain at 107 d and feed efficiency at 44, 73, and 107 d. However, these associations were not simultaneously found in both strains suggesting that they might have been produced by linkage disequilibrium with another mutation located in the IGF1 locus or another linked gene. Since the PN and MN strains differ very markedly on their feed intake, the chicken leptin gene was included in the sequence analysis. Unfortunately, attempts to amplify several regions of this gene were unsuccessful. Even when primers complementary to highly conserved regions were used, the PCR consistently failed. Other authors have reported similar problems when trying to amplify avian leptin sequencesca
dc.description.sponsorshipThis research was funded by the Spanish Ministry of Education and Culture (CICYT AGF99-1221)ca
dc.format.extent9ca
dc.language.isoengca
dc.publisherElsevierca
dc.relation.ispartofPoultry Scienceca
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleIdentification of Three Single Nucleotide Polymorphisms in the Chicken Insulin-Like Growth Factor 1 and 2 Genes and Their Associations with Growth and Feeding Traitsca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDCICYT/ /AGF99-1221/ES/ /ca
dc.subject.udc575ca
dc.identifier.doihttps://doi.org/10.1093/ps/82.10.1485ca
dc.contributor.groupGenètica i Millora Animalca


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