Diversity analysis of cotton (Gossypium hirsutum L.) germplasm using the CottonSNP63K Array. Issue 1 (December 2017)

• Record Type: Journal Article
• Authors: Hinze, Lori; Hulse-Kemp, Amanda; Wilson, Iain; Zhu, Qian-Hao; Llewellyn, Danny; Taylor, Jen; Spriggs, Andrew; Fang, David; Ulloa, Mauricio; Burke, John; Giband, Marc; Lacape, Jean-Marc; Van Deynze, Allen; Udall, Joshua; Scheffler, Jodi; Hague, Steve; Wendel, Jonathan; Pepper, Alan; Frelichowski, James; Lawley, Cindy; Jones, Don; Percy, Richard; Stelly, David
• Is Part Of: BMC plant biology. Volume 17:Issue 1(2017)
• Page Start: 1
• Page End: 20
• Publication Date: 2017-12
• Subjects: Breeding -- Cotton -- Diversity analysis -- Genome-wide association analysis -- Germplasm collection -- Molecular markers -- Seed protein content; Plant molecular biology -- Periodicals; Botany -- Periodicals; 580.5
• DOI: 10.1186/s12870-017-0981-y
• Languages: English
• ISSNs: 1471-2229

Abstract

Abstract Background Cotton germplasm resources contain beneficial alleles that can be exploited to develop germplasm adapted to emerging environmental and climate conditions. Accessions and lines have traditionally been characterized based on phenotypes, but phenotypic profiles are limited by the cost, time, and space required to make visual observations and measurements. With advances in molecular genetic methods, genotypic profiles are increasingly able to identify differences among accessions due to the larger number of genetic markers that can be measured. A combination of both methods would greatly enhance our ability to characterize germplasm resources. Recent efforts have culminated in the identification of sufficient SNP markers to establish high-throughput genotyping systems, such as the CottonSNP63K array, which enables a researcher to efficiently analyze large numbers of SNP markers and obtain highly repeatable results. In the current investigation, we have utilized the SNP array for analyzing genetic diversity primarily among cotton cultivars, making comparisons to SSR-based phylogenetic analyses, and identifying loci associated with seed nutritional traits. Results The SNP markers distinctly separatedG. hirsutum from otherGossypium species and distinguished the wild from cultivated types ofG. hirsutum . The markers also efficiently discerned differences among cultivars, which was the primary goal when designing the CottonSNP63K array. Population structure within the genus compared favorably with previous results obtained using SSR markers, and an association study identified loci linked to factors that affect cottonseed protein content. Conclusions Our results provide a large genome-wide variation data set for primarily cultivated cotton. Thousands of SNPs in representative cotton genotypes provide an opportunity to finely discriminate among cultivated cotton from around the world. The SNPs will be relevant as dense markers of genome variation for association mapping approaches aimed at correlating molecular polymorphisms with variation in phenotypic traits, as well as for molecular breeding approaches in cotton.