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AOX – A potential marker for efficient rooting of olive shoot cuttings.

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Detalhes bibliográficos
Resumo:Alternative oxidase (AOX) is recently suggested to be a potential candidate as functional marker for efficient cell reprogramming under stress (Arnholdt-Schmitt et al., 2006a). The presented work is part of a Marie Curie Chair project, that was established to investigate the potential role of the multigene AOX to assist breeding on efficient rooting of olive shoot cuttings (Arnholdt-Schmitt et al. 2006b). Plant mito-chondrial AOX is a small nuclear-encoded multigene family consisting of the two subfamilies AOX1 and AOX2. The intron-exon structure of AOX has been well characterized in several species, revealing a large degree of conservation. Here we report for the first time about the isolation of AOX multigene se-quences of olive (Olea europaea L.). The genes were isolated from a portuguese clone of the landrace ‘Galega vulgar’.
Autores principais:Arnholdt-Schmitt, Birgit
Outros Autores:Santos Macedo, Elisete; Cardoso, Hélia; Peixe, Augusto; Cordeiro, António M.
Ano:2011
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade de Évora
Idioma:português
Origem:Repositório Científico da Universidade de Évora
Descrição
Resumo:Alternative oxidase (AOX) is recently suggested to be a potential candidate as functional marker for efficient cell reprogramming under stress (Arnholdt-Schmitt et al., 2006a). The presented work is part of a Marie Curie Chair project, that was established to investigate the potential role of the multigene AOX to assist breeding on efficient rooting of olive shoot cuttings (Arnholdt-Schmitt et al. 2006b). Plant mito-chondrial AOX is a small nuclear-encoded multigene family consisting of the two subfamilies AOX1 and AOX2. The intron-exon structure of AOX has been well characterized in several species, revealing a large degree of conservation. Here we report for the first time about the isolation of AOX multigene se-quences of olive (Olea europaea L.). The genes were isolated from a portuguese clone of the landrace ‘Galega vulgar’.