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Article|01 Apr 2018|OPEN
Molecular markers reliably predict post-harvest deterioration of fresh-cut lettuce in modified atmosphere packaging
Ivan Simko1 , , Ryan J. Hayes2 , Maria-Jose Truco3 , Richard W. Michelmore3 , Rudie Antonise4 and Mark Massoudi,5
1U.S. Department of Agriculture, Agricultural Research Service, U.S. Agricultural Research Station, Crop Improvement and Protection Research Unit, 1636 East Alisal Street, Salinas, CA 93905, USA
2U.S. Department of Agriculture, National Forage Seed Production Research Center, 3450 SW Campus Way, Corvallis, OR 97331, USA
3The Genome Center and Department of Plant Sciences, University of California, Davis, CA 95616, USA
4KeyGene N.V., P.O. Box 2166700 AE Wageningen, The Netherlands
5Ag-Biotech, 9701 Blue Larkspur Lane, Suite A, Monterey, CA 93940, USA
*Corresponding author. E-mail: ivan.simko@ars.usda.gov

Horticulture Research 5,
Article number: 21 (2018)
doi: https://doi.org/10.1038/s41438-018-0022-5
Views: 1028

Received: 03 Dec 2017
Revised: 06 Feb 2018
Accepted: 13 Feb 2018
Published online: 01 Apr 2018

Abstract

Fresh-cut lettuce is popular, but highly perishable product. Genetic studies of two bi-parental populations derived from crossing parents with rapid and slow rates of deterioration showed that the deterioration rate is a heritable trait (broad spectrum heritability, H2 of 0.56–0.87). The major genetic determinant of the deterioration rate in both populations was the quantitative trait locus (QTL), qSL4, located on linkage group 4. This QTL explained 40–74% of the total phenotypic variation of the trait in the two populations. Saturating the qSL4 region with single-nucleotide (SNP) markers allowed detection of six haplotypes in a set of 16 lettuce accessions with different rates of deterioration. Three of the haplotypes were always associated with very rapid rates of deterioration, while the other three haplotypes were associated with slow rates of deterioration. Two SNPs located 53 bp apart were sufficient to separate the 16 accessions into two groups with different rates of deterioration. The accuracy of markers-trait association was subsequently tested on 350 plants from seven F2 families that originated from crossing parents with different rates of deterioration. The H2 of deterioration rate in these seven families ranged from 0.64 to 0.90. The SNP-based analysis accurately identified individuals with rapid, intermediate, and slow rates of deterioration in each family. Intermediate rate of deterioration was found in individuals having heterozygous alleles at qSL4, indicating an additive effect of the alleles. The assay can be used for fast, accurate, and reliable identification of deterioration rate after processing for salad.