4.3 Article

Genotyping-by-sequencing and genomic selection applications in hexaploid triticale

Journal

G3-GENES GENOMES GENETICS
Volume 12, Issue 2, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/g3journal/jkab413

Keywords

genotyping-by-sequencing (GBS); genomic selection (GS); linkage disequilibrium (LD); population genetics; triticale

Funding

  1. Foundation for Food and Agriculture Research [0001]
  2. Noble Research Institute, LLC

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Triticale, a hybrid species between wheat and rye, has a limited genomic resource due to its large and complex genome. This study used genotyping-by-sequencing to generate dense marker data and identified a large number of single nucleotide polymorphism markers. Genetic diversity and population structure analysis provided insights into the genetic background and population composition of triticale. Additionally, genomic selection models were used to estimate the accuracy of improving forage yield in triticale, showing the potential of genomic selection in triticale breeding.
Triticale, a hybrid species between wheat and rye, is one of the newest additions to the plant kingdom with a very short history of improvement. It has very limited genomic resources because of its large and complex genome. Objectives of this study were to generate dense marker data, understand genetic diversity, population structure, linkage disequilibrium (LD), and estimate accuracies of commonly used genomic selection (GS) models on forage yield of triticale. Genotyping-by-sequencing (GBS), using PstI and MspI restriction enzymes for reducing genome complexity, was performed on a triticale diversity panel (n = 289). After filtering for biallelic loci with more than 70% genome coverage, and minor allele frequency (MAF) > 0.05, de novo variant calling identified 16,378 single nucleotide polymorphism (SNP) markers. Sequences of these variants were mapped to wheat and rye reference genomes to infer their homologous groups and chromosome positions. About 45% (7430), and 58% (9500) of the de novo identified SNPs were mapped to the wheat and rye reference genomes, respectively. Interestingly, 28.9% (2151) of the 7430 SNPs were mapped to the D genome of hexaploid wheat, indicating substantial substitution of the R genome with D genome in cultivated triticale. About 27% of marker pairs were in significant LD with an average r(2) > 0.18 (P < 0.05). Genome-wide LD declined rapidly to r(2) < 0.1 beyond 10 kb physical distance. The three sub-genomes (A, B, and R) showed comparable LD decay patterns. Genetic diversity and population structure analyses identified five distinct clusters. Genotype grouping did not follow prior winter vs spring-type classification. However, one of the clusters was largely dominated by winter triticale. GS accuracies were estimated for forage yield using three commonly used models with different training population sizes and marker densities. GS accuracy increased with increasing training population size while gain in accuracy tended to plateau with marker densities of 2000 SNPs or more. Average GS accuracy was about 0.52, indicating the potential of using GS in triticale forage yield improvement.

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