Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo

Detalhes bibliográficos
Autor(a) principal: Currais, Lara
Data de Publicação: 2013
Outros Autores: Loureiro, J., Santos, Conceição, Canhoto, J. M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/25784
https://doi.org/10.1007/s11240-013-0311-5
Resumo: Ploidy levels of short-term (1 and 2 years) and long-term (7 and 10 years) embryogenic cultures as well as of regenerated plantlets of tamarillo were analyzed by flow cytometry and chromosome counts. Embryogenic cultures were induced from expanding leaves cultured in the presence of Picloram or 2,4-dichlorophenoxyacetic acid (2,4-D) and monthly subcultured on the same media. Embryo development and plantlets were obtained following subculture of the embryogenic tissue in auxin free medium containing gibberellic acid (GA3). Seedlings and rooted shoots from axillary shoot proliferation were used as controls. The results showed that in long-term embryogenic cultures the ability to develop somatic embryos and plantlets was reduced. Embryogenic tissues maintained for 10 years were mostly aneuploids of the tetraploid (2n = 4x = 48) level whereas those kept in culture for 7 years or less were also mostly aneuploids but of the diploid (2n = 2x = 24) level. The results obtained by flow cytometry were, in general, consistent with those obtained by chromosome counts. The chromosome alteration observed in the embryogenic tissues was already present after 1 year of culture and increased with culture age, hence impairing the maintenance of these tissues for long periods without affecting chromosome stability of the regenerated plantlets. However, the occurrence of triploids and tetraploids as well as aneuploids can be useful for breeding purposes. A value around 23 pg/2C was found for the genome size of tamarillo largely exceeding the value previously published (15.50 pg/2C).
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spelling Ploidy stability in embryogenic cultures and regenerated plantlets of tamarilloCyphomandra betaceaAneuploidsMixoploidsNuclear DNA contentSomatic embryogenesisPloidy levels of short-term (1 and 2 years) and long-term (7 and 10 years) embryogenic cultures as well as of regenerated plantlets of tamarillo were analyzed by flow cytometry and chromosome counts. Embryogenic cultures were induced from expanding leaves cultured in the presence of Picloram or 2,4-dichlorophenoxyacetic acid (2,4-D) and monthly subcultured on the same media. Embryo development and plantlets were obtained following subculture of the embryogenic tissue in auxin free medium containing gibberellic acid (GA3). Seedlings and rooted shoots from axillary shoot proliferation were used as controls. The results showed that in long-term embryogenic cultures the ability to develop somatic embryos and plantlets was reduced. Embryogenic tissues maintained for 10 years were mostly aneuploids of the tetraploid (2n = 4x = 48) level whereas those kept in culture for 7 years or less were also mostly aneuploids but of the diploid (2n = 2x = 24) level. The results obtained by flow cytometry were, in general, consistent with those obtained by chromosome counts. The chromosome alteration observed in the embryogenic tissues was already present after 1 year of culture and increased with culture age, hence impairing the maintenance of these tissues for long periods without affecting chromosome stability of the regenerated plantlets. However, the occurrence of triploids and tetraploids as well as aneuploids can be useful for breeding purposes. A value around 23 pg/2C was found for the genome size of tamarillo largely exceeding the value previously published (15.50 pg/2C).This work was supported by the Portuguese Foundation for Science and Technology (FCT).Springer Science2013info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/25784http://hdl.handle.net/10316/25784https://doi.org/10.1007/s11240-013-0311-5enghttp://link.springer.com/article/10.1007%2Fs11240-013-0311-5Currais, LaraLoureiro, J.Santos, ConceiçãoCanhoto, J. M.info: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:RCAAP2020-05-25T09:41:28Zoai:estudogeral.uc.pt:10316/25784Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:56:05.692495Repositório 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 Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
title Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
spellingShingle Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
Currais, Lara
Cyphomandra betacea
Aneuploids
Mixoploids
Nuclear DNA content
Somatic embryogenesis
title_short Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
title_full Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
title_fullStr Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
title_full_unstemmed Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
title_sort Ploidy stability in embryogenic cultures and regenerated plantlets of tamarillo
author Currais, Lara
author_facet Currais, Lara
Loureiro, J.
Santos, Conceição
Canhoto, J. M.
author_role author
author2 Loureiro, J.
Santos, Conceição
Canhoto, J. M.
author2_role author
author
author
dc.contributor.author.fl_str_mv Currais, Lara
Loureiro, J.
Santos, Conceição
Canhoto, J. M.
dc.subject.por.fl_str_mv Cyphomandra betacea
Aneuploids
Mixoploids
Nuclear DNA content
Somatic embryogenesis
topic Cyphomandra betacea
Aneuploids
Mixoploids
Nuclear DNA content
Somatic embryogenesis
description Ploidy levels of short-term (1 and 2 years) and long-term (7 and 10 years) embryogenic cultures as well as of regenerated plantlets of tamarillo were analyzed by flow cytometry and chromosome counts. Embryogenic cultures were induced from expanding leaves cultured in the presence of Picloram or 2,4-dichlorophenoxyacetic acid (2,4-D) and monthly subcultured on the same media. Embryo development and plantlets were obtained following subculture of the embryogenic tissue in auxin free medium containing gibberellic acid (GA3). Seedlings and rooted shoots from axillary shoot proliferation were used as controls. The results showed that in long-term embryogenic cultures the ability to develop somatic embryos and plantlets was reduced. Embryogenic tissues maintained for 10 years were mostly aneuploids of the tetraploid (2n = 4x = 48) level whereas those kept in culture for 7 years or less were also mostly aneuploids but of the diploid (2n = 2x = 24) level. The results obtained by flow cytometry were, in general, consistent with those obtained by chromosome counts. The chromosome alteration observed in the embryogenic tissues was already present after 1 year of culture and increased with culture age, hence impairing the maintenance of these tissues for long periods without affecting chromosome stability of the regenerated plantlets. However, the occurrence of triploids and tetraploids as well as aneuploids can be useful for breeding purposes. A value around 23 pg/2C was found for the genome size of tamarillo largely exceeding the value previously published (15.50 pg/2C).
publishDate 2013
dc.date.none.fl_str_mv 2013
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/10316/25784
http://hdl.handle.net/10316/25784
https://doi.org/10.1007/s11240-013-0311-5
url http://hdl.handle.net/10316/25784
https://doi.org/10.1007/s11240-013-0311-5
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://link.springer.com/article/10.1007%2Fs11240-013-0311-5
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dc.publisher.none.fl_str_mv Springer Science
publisher.none.fl_str_mv Springer Science
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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