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Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis

Enzymatic discoloration (ED) of potato tubers was investigated in an attempt to unravel the underlying genetic factors. Both enzyme and substrate concentration have been reported to influence the degree of discoloration and as such this trait can be regarded as polygenic. The diploid mapping populat...

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Autores principales: Werij, Jeroen S., Kloosterman, Bjorn, Celis-Gamboa, Carolina, de Vos, C. H. Ric, America, Twan, Visser, Richard G. F., Bachem, Christian W. B.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913181/
https://www.ncbi.nlm.nih.gov/pubmed/17492422
http://dx.doi.org/10.1007/s00122-007-0560-y
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author Werij, Jeroen S.
Kloosterman, Bjorn
Celis-Gamboa, Carolina
de Vos, C. H. Ric
America, Twan
Visser, Richard G. F.
Bachem, Christian W. B.
author_facet Werij, Jeroen S.
Kloosterman, Bjorn
Celis-Gamboa, Carolina
de Vos, C. H. Ric
America, Twan
Visser, Richard G. F.
Bachem, Christian W. B.
author_sort Werij, Jeroen S.
collection PubMed
description Enzymatic discoloration (ED) of potato tubers was investigated in an attempt to unravel the underlying genetic factors. Both enzyme and substrate concentration have been reported to influence the degree of discoloration and as such this trait can be regarded as polygenic. The diploid mapping population C × E, consisting of 249 individuals, was assayed for the degree of ED and levels of chlorogenic acid and tyrosine. Using this data, Quantitative Trait Locus (QTL) analysis was performed. Three QTLs for ED have been found on parental chromosomes C3, C8, E1, and E8. For chlorogenic acid a QTL has been identified on C2 and for tyrosine levels, a QTL has been detected on C8. None of the QTLs overlap, indicating the absence of genetic correlations between these components underlying ED, in contrast to earlier reports in literature. An obvious candidate gene for the QTL for ED on Chromosome 8 is polyphenol oxidase (PPO), which was previously mapped on chromosome 8. With gene-specific primers for PPO gene POT32 a CAPS marker was developed. Three different alleles (POT32-1, -2, and -3) could be discriminated. The segregating POT32 alleles were used to map the POT32 CAPS marker and QTL analysis was redone, showing that POT32 coincides with the QTL peak. A clear correlation between allele combinations and degree of discoloration was observed. In addition, analysis of POT32 gene expression in a subset of genotypes indicated a correlation between the level of gene expression and allele composition. On average, genotypes having two copies of allele 1 had both the highest degree of discoloration as well as the highest level of POT32 gene expression.
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spelling pubmed-19131812007-07-09 Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis Werij, Jeroen S. Kloosterman, Bjorn Celis-Gamboa, Carolina de Vos, C. H. Ric America, Twan Visser, Richard G. F. Bachem, Christian W. B. Theor Appl Genet Original Paper Enzymatic discoloration (ED) of potato tubers was investigated in an attempt to unravel the underlying genetic factors. Both enzyme and substrate concentration have been reported to influence the degree of discoloration and as such this trait can be regarded as polygenic. The diploid mapping population C × E, consisting of 249 individuals, was assayed for the degree of ED and levels of chlorogenic acid and tyrosine. Using this data, Quantitative Trait Locus (QTL) analysis was performed. Three QTLs for ED have been found on parental chromosomes C3, C8, E1, and E8. For chlorogenic acid a QTL has been identified on C2 and for tyrosine levels, a QTL has been detected on C8. None of the QTLs overlap, indicating the absence of genetic correlations between these components underlying ED, in contrast to earlier reports in literature. An obvious candidate gene for the QTL for ED on Chromosome 8 is polyphenol oxidase (PPO), which was previously mapped on chromosome 8. With gene-specific primers for PPO gene POT32 a CAPS marker was developed. Three different alleles (POT32-1, -2, and -3) could be discriminated. The segregating POT32 alleles were used to map the POT32 CAPS marker and QTL analysis was redone, showing that POT32 coincides with the QTL peak. A clear correlation between allele combinations and degree of discoloration was observed. In addition, analysis of POT32 gene expression in a subset of genotypes indicated a correlation between the level of gene expression and allele composition. On average, genotypes having two copies of allele 1 had both the highest degree of discoloration as well as the highest level of POT32 gene expression. Springer-Verlag 2007-05-11 2007-07 /pmc/articles/PMC1913181/ /pubmed/17492422 http://dx.doi.org/10.1007/s00122-007-0560-y Text en © Springer-Verlag 2007
spellingShingle Original Paper
Werij, Jeroen S.
Kloosterman, Bjorn
Celis-Gamboa, Carolina
de Vos, C. H. Ric
America, Twan
Visser, Richard G. F.
Bachem, Christian W. B.
Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis
title Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis
title_full Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis
title_fullStr Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis
title_full_unstemmed Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis
title_short Unravelling enzymatic discoloration in potato through a combined approach of candidate genes, QTL, and expression analysis
title_sort unravelling enzymatic discoloration in potato through a combined approach of candidate genes, qtl, and expression analysis
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1913181/
https://www.ncbi.nlm.nih.gov/pubmed/17492422
http://dx.doi.org/10.1007/s00122-007-0560-y
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