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resumen

Resumen
In purple carrots, anthocyanin pigmentation can be expressed in the entire root, or it can display tissue specific-patterns. Within the phloem, purple pigmentation can be found in the outer phloem (OP) (also called the cortex) and inner phloem (IP), or it can be confined exclusively to the OP. In this work, the genetic control underlying tissue-specific anthocyanin pigmentation in the carrot root OP and IP tissues was investigated by means of linkage [ver mas...]
dc.contributor.authorBannoud, Florencia
dc.contributor.authorCarvajal, Sofía
dc.contributor.authorEllison, Shelby L.
dc.contributor.authorSenalik, Douglas A.
dc.contributor.authorGomez Talquenca, Gonzalo
dc.contributor.authorIorizzo, Massimo
dc.contributor.authorSimon, Philipp W.
dc.contributor.authorCavagnaro, Pablo
dc.date.accessioned2022-06-07T11:24:00Z
dc.date.available2022-06-07T11:24:00Z
dc.date.issued2021-09
dc.identifier.issn2073-4425
dc.identifier.otherhttps://doi.org/10.3390/genes12101464
dc.identifier.urihttp://hdl.handle.net/20.500.12123/12033
dc.identifier.urihttps://www.mdpi.com/2073-4425/12/10/1464
dc.description.abstractIn purple carrots, anthocyanin pigmentation can be expressed in the entire root, or it can display tissue specific-patterns. Within the phloem, purple pigmentation can be found in the outer phloem (OP) (also called the cortex) and inner phloem (IP), or it can be confined exclusively to the OP. In this work, the genetic control underlying tissue-specific anthocyanin pigmentation in the carrot root OP and IP tissues was investigated by means of linkage mapping and transcriptome (RNA-seq) and phylogenetic analyses; followed by gene expression (RT-qPCR) evaluations in two genetic backgrounds, an F2 population (3242) and the inbred B7262. Genetic mapping of ‘root outer phloem anthocyanin pigmentation’ (ROPAP) and inner phloem pigmentation (RIPAP) revealed colocalization of ROPAP with the P1 and P3 genomic regions previously known to condition pigmentation in different genetic stocks, whereas RIPAP co-localized with P3 only. Transcriptome analysis of purple OP (POP) vs. non-purple IP (NPIP) tissues, along with linkage and phylogenetic data, allowed an initial identification of 28 candidate genes, 19 of which were further evaluated by RT-qPCR in independent root samples of 3242 and B7262, revealing 15 genes consistently upregulated in the POP in both genetic backgrounds, and two genes upregulated in the POP in specific backgrounds. These include seven transcription factors, seven anthocyanin structural genes, and two genes involved in cellular transport. Altogether, our results point at DcMYB7, DcMYB113, and a MADS-box (DCAR_010757) as the main candidate genes conditioning ROPAP in 3242, whereas DcMYB7 and MADS-box condition RIPAP in this background. In 7262, DcMYB113 conditions ROPAP.eng
dc.formatapplication/pdfes_AR
dc.language.isoenges_AR
dc.publisherMDPIes_AR
dc.rightsinfo:eu-repo/semantics/openAccesses_AR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.sourceGenes 12 (10) : 1464 (2021)es_AR
dc.subjectZanahoriaes_AR
dc.subjectCarrotseng
dc.subjectDaucus carotaes_AR
dc.subjectVariedadeses_AR
dc.subjectVarietieseng
dc.subjectPigmentaciónes_AR
dc.subjectPigmentationeng
dc.subjectAntocianinases_AR
dc.subjectAnthocyaninseng
dc.subjectFloemaes_AR
dc.subjectPhloemeng
dc.subjectGenéticaes_AR
dc.subjectGeneticseng
dc.titleGenetic and Transcription Profile Analysis of Tissue-Specific Anthocyanin Pigmentation in Carrot Root Phloemes_AR
dc.typeinfo:ar-repo/semantics/artículoes_AR
dc.typeinfo:eu-repo/semantics/articlees_AR
dc.typeinfo:eu-repo/semantics/publishedVersiones_AR
dc.rights.licenseCreative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
dc.description.origenEEA Mendozaes_AR
dc.description.filFil: Bannoud, Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Carvajal, Sofía. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Ellison, Shelby. University of Wisconsin. Department of Horticulture; Estados Unidos.es_AR
dc.description.filFil: Senalik, Douglas A. United States Department of Agriculture–Agricultural Research Service. Vegetable Crops Research Unit; Estados Unidoses_AR
dc.description.filFil: Gomez Talquenca, Gonzalo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Mendoza; Argentinaes_AR
dc.description.filFil: Iorizzo, Massimo. North Carolina State University. Plants for Human Health Institute; Estados Unidoses_AR
dc.description.filFil: Iorizzo, Massimo. North Carolina State University. Department of Horticultural Science; Estados Unidoses_AR
dc.description.filFil: Simon, Philipp. University of Wisconsin. Department of Horticulture; Estados Unidos.es_AR
dc.description.filFil: Simon, Philipp. United States Department of Agriculture–Agricultural Research Service. Vegetable Crops Research Unit; Estados Unidoses_AR
dc.description.filFil: Cavagnaro, Pablo. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria La Consulta; Argentinaes_AR
dc.description.filFil: Cavagnaro, Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentinaes_AR
dc.description.filFil: Cavagnaro, Pablo. Universidad Nacional de Cuyo. Facultad de Ciencias Agrarias. Instituto de Horticultura; Argentina.es_AR
dc.subtypecientifico


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