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Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach
Peach flesh color (white or yellow) is among the most popular commercial criteria for peach classification, and has implications for consumer acceptance and fruit nutritional quality. Despite the increasing interest in improving cultivars of both flesh types, little is known about the genetic basis...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223380/ https://www.ncbi.nlm.nih.gov/pubmed/23855972 http://dx.doi.org/10.1111/tpj.12283 |
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author | Falchi, Rachele Vendramin, Elisa Zanon, Laura Scalabrin, Simone Cipriani, Guido Verde, Ignazio Vizzotto, Giannina Morgante, Michele |
author_facet | Falchi, Rachele Vendramin, Elisa Zanon, Laura Scalabrin, Simone Cipriani, Guido Verde, Ignazio Vizzotto, Giannina Morgante, Michele |
author_sort | Falchi, Rachele |
collection | PubMed |
description | Peach flesh color (white or yellow) is among the most popular commercial criteria for peach classification, and has implications for consumer acceptance and fruit nutritional quality. Despite the increasing interest in improving cultivars of both flesh types, little is known about the genetic basis for the carotenoid content diversity in peach. Here we describe the association between genotypes at a locus encoding the carotenoid cleavage dioxygenase 4 (PpCCD4), localized in pseudomolecule 1 of the Prunus persica reference genome sequence, and the flesh color for 37 peach varieties, including two somatic revertants, and three ancestral relatives of peach, providing definitive evidence that this locus is responsible for flesh color phenotype. We show that yellow peach alleles have arisen from various ancestral haplotypes by at least three independent mutational events involving nucleotide substitutions, small insertions and transposable element insertions, and that these mutations, despite being located within the transcribed portion of the gene, also result in marked differences in transcript levels, presumably as a consequence of differential transcript stability involving nonsense-mediated mRNA decay. The PpCCD4 gene provides a unique example of a gene for which humans, in their quest to diversify phenotypic appearance and qualitative characteristics of a fruit, have been able to select and exploit multiple mutations resulting from a variety of mechanisms. |
format | Online Article Text |
id | pubmed-4223380 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42233802014-12-12 Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach Falchi, Rachele Vendramin, Elisa Zanon, Laura Scalabrin, Simone Cipriani, Guido Verde, Ignazio Vizzotto, Giannina Morgante, Michele Plant J Featured Article Peach flesh color (white or yellow) is among the most popular commercial criteria for peach classification, and has implications for consumer acceptance and fruit nutritional quality. Despite the increasing interest in improving cultivars of both flesh types, little is known about the genetic basis for the carotenoid content diversity in peach. Here we describe the association between genotypes at a locus encoding the carotenoid cleavage dioxygenase 4 (PpCCD4), localized in pseudomolecule 1 of the Prunus persica reference genome sequence, and the flesh color for 37 peach varieties, including two somatic revertants, and three ancestral relatives of peach, providing definitive evidence that this locus is responsible for flesh color phenotype. We show that yellow peach alleles have arisen from various ancestral haplotypes by at least three independent mutational events involving nucleotide substitutions, small insertions and transposable element insertions, and that these mutations, despite being located within the transcribed portion of the gene, also result in marked differences in transcript levels, presumably as a consequence of differential transcript stability involving nonsense-mediated mRNA decay. The PpCCD4 gene provides a unique example of a gene for which humans, in their quest to diversify phenotypic appearance and qualitative characteristics of a fruit, have been able to select and exploit multiple mutations resulting from a variety of mechanisms. BlackWell Publishing Ltd 2013-10 2013-08-08 /pmc/articles/PMC4223380/ /pubmed/23855972 http://dx.doi.org/10.1111/tpj.12283 Text en © 2013 The Authors The Plant Journal © 2013 John Wiley & Sons Ltd http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Featured Article Falchi, Rachele Vendramin, Elisa Zanon, Laura Scalabrin, Simone Cipriani, Guido Verde, Ignazio Vizzotto, Giannina Morgante, Michele Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
title | Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
title_full | Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
title_fullStr | Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
title_full_unstemmed | Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
title_short | Three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
title_sort | three distinct mutational mechanisms acting on a single gene underpin the origin of yellow flesh in peach |
topic | Featured Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223380/ https://www.ncbi.nlm.nih.gov/pubmed/23855972 http://dx.doi.org/10.1111/tpj.12283 |
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