Societal Impact Statement
The English West Country is the home of cider making, providing the region with jobs and industry, as well as cultural reference points such as Laurie Lee's Cider with Rosie. Many important cider apple varieties were developed at Long Ashton Research Station (LARS), near Bristol, UK, including 29 varieties known collectively as ‘The Girls’. After its closure, some of the knowledge and expertise acquired at Long Ashton was lost, including the pedigree of ‘The Girls’. We sampled LARS’ derived trees and, using a novel genotyping technique, rediscovered the pedigree of ‘The Girls’, ensuring that this important cider apple collection will be available for future generations.
Summary
Our research had two objectives: (a) record the influence of Long Ashton Research Station on the introduction of new cider apple cultivars to the UK; (b) rediscover the parentage of the cider apple cultivars known collectively as ‘The Girls’.
For rapid, cost effective and accurate genotyping, we used the recently developed, medium density, single nucleotide polymorphism‐based genotyping procedure, SEQSNP®, to characterize the cultivars.
We generated a medium density (1,500 markers), whole genome genotype for 245 apple cultivars that allowed us to determine the relationship between cultivars and, in so doing, rediscover the parentage of ‘The Girls’.
We show that SNP genotyping is an efficient tool for the analysis of genetic diversity in cider apples and apples in general, and that the cider apple breeding programme carried out at Long Ashton Research Station made, and continues to make, a unique contribution to UK cider production.
Accurate identification of named accessions in germplasm collections is extremely important, especially for vegetatively propagated crops which are expensive to maintain. Thus, an inexpensive, reliable, and rapid genotyping method is essential because it avoids the need for laborious and time-consuming morphological comparisons. Single Nucleotide Polymorphism (SNP) marker panels containing large numbers of SNPs have been developed for many crop species, but such panels are much too large for basic cultivar identification. Here, we have identified a minimum set of SNP markers sufficient to distinguish apple cultivars held in the English and Welsh national collections providing a cheaper and automatable alternative to the markers currently used by the community. We show that SNP genotyping with a small set of well selected markers is equally efficient as microsatellites for the identification of apple cultivars and has the added advantage of automation and reduced cost when screening large numbers of samples.
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