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Genetic, metabolite and developmental determinism of fruit friction discolouration in pear
BACKGROUND: The unattractive appearance of the surface of pear fruit caused by the postharvest disorder friction discolouration (FD) is responsible for significant consumer dissatisfaction in markets, leading to lower returns to growers. Developing an understanding of the genetic control of FD is es...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177423/ https://www.ncbi.nlm.nih.gov/pubmed/25224302 http://dx.doi.org/10.1186/s12870-014-0241-3 |
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author | Saeed, Munazza Brewer, Lester Johnston, Jason McGhie, Tony K Gardiner, Susan E Heyes, Julian A Chagné, David |
author_facet | Saeed, Munazza Brewer, Lester Johnston, Jason McGhie, Tony K Gardiner, Susan E Heyes, Julian A Chagné, David |
author_sort | Saeed, Munazza |
collection | PubMed |
description | BACKGROUND: The unattractive appearance of the surface of pear fruit caused by the postharvest disorder friction discolouration (FD) is responsible for significant consumer dissatisfaction in markets, leading to lower returns to growers. Developing an understanding of the genetic control of FD is essential to enable the full application of genomics-informed breeding for the development of new pear cultivars. Biochemical constituents [phenolic compounds and ascorbic acid (AsA)], polyphenol oxidase (PPO) activity, as well as skin anatomy, have been proposed to play important roles in FD susceptibility in studies on a limited number of cultivars. However, to date there has been no investigation on the biochemical and genetic control of FD, employing segregating populations. In this study, we used 250 seedlings from two segregating populations (POP369 and POP356) derived from interspecific crosses between Asian (Pyrus pyrifolia Nakai and P. bretschneideri Rehd.) and European (P. communis) pears to identify genetic factors associated with susceptibility to FD. RESULTS: Single nucleotide polymorphism (SNP)-based linkage maps suitable for QTL analysis were developed for the parents of both populations. The maps for population POP369 comprised 174 and 265 SNP markers for the male and female parent, respectively, while POP356 maps comprised 353 and 398 SNP markers for the male and female parent, respectively. Phenotypic data for 22 variables were measured over two successive years (2011 and 2012) for POP369 and one year (2011) only for POP356. A total of 221 QTLs were identified that were linked to 22 phenotyped variables, including QTLs associated with FD for both populations that were stable over the successive years. In addition, clear evidence of the influence of developmental factors (fruit maturity) on FD and other variables was also recorded. CONCLUSIONS: The QTLs associated with fruit firmness, PPO activity, AsA concentration and concentration of polyphenol compounds as well as FD are the first reported for pear. We conclude that the postharvest disorder FD is controlled by multiple small effect QTLs and that it will be very challenging to apply marker-assisted selection based on these QTLs. However, genomic selection could be employed to select elite genotypes with lower or no susceptibility to FD early in the breeding cycle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0241-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4177423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41774232014-09-29 Genetic, metabolite and developmental determinism of fruit friction discolouration in pear Saeed, Munazza Brewer, Lester Johnston, Jason McGhie, Tony K Gardiner, Susan E Heyes, Julian A Chagné, David BMC Plant Biol Research Article BACKGROUND: The unattractive appearance of the surface of pear fruit caused by the postharvest disorder friction discolouration (FD) is responsible for significant consumer dissatisfaction in markets, leading to lower returns to growers. Developing an understanding of the genetic control of FD is essential to enable the full application of genomics-informed breeding for the development of new pear cultivars. Biochemical constituents [phenolic compounds and ascorbic acid (AsA)], polyphenol oxidase (PPO) activity, as well as skin anatomy, have been proposed to play important roles in FD susceptibility in studies on a limited number of cultivars. However, to date there has been no investigation on the biochemical and genetic control of FD, employing segregating populations. In this study, we used 250 seedlings from two segregating populations (POP369 and POP356) derived from interspecific crosses between Asian (Pyrus pyrifolia Nakai and P. bretschneideri Rehd.) and European (P. communis) pears to identify genetic factors associated with susceptibility to FD. RESULTS: Single nucleotide polymorphism (SNP)-based linkage maps suitable for QTL analysis were developed for the parents of both populations. The maps for population POP369 comprised 174 and 265 SNP markers for the male and female parent, respectively, while POP356 maps comprised 353 and 398 SNP markers for the male and female parent, respectively. Phenotypic data for 22 variables were measured over two successive years (2011 and 2012) for POP369 and one year (2011) only for POP356. A total of 221 QTLs were identified that were linked to 22 phenotyped variables, including QTLs associated with FD for both populations that were stable over the successive years. In addition, clear evidence of the influence of developmental factors (fruit maturity) on FD and other variables was also recorded. CONCLUSIONS: The QTLs associated with fruit firmness, PPO activity, AsA concentration and concentration of polyphenol compounds as well as FD are the first reported for pear. We conclude that the postharvest disorder FD is controlled by multiple small effect QTLs and that it will be very challenging to apply marker-assisted selection based on these QTLs. However, genomic selection could be employed to select elite genotypes with lower or no susceptibility to FD early in the breeding cycle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12870-014-0241-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-16 /pmc/articles/PMC4177423/ /pubmed/25224302 http://dx.doi.org/10.1186/s12870-014-0241-3 Text en © Saeed et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Saeed, Munazza Brewer, Lester Johnston, Jason McGhie, Tony K Gardiner, Susan E Heyes, Julian A Chagné, David Genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
title | Genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
title_full | Genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
title_fullStr | Genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
title_full_unstemmed | Genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
title_short | Genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
title_sort | genetic, metabolite and developmental determinism of fruit friction discolouration in pear |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177423/ https://www.ncbi.nlm.nih.gov/pubmed/25224302 http://dx.doi.org/10.1186/s12870-014-0241-3 |
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