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A PCR Marker for Growth Habit in Common Wheat Based on Allelic Variation at the VRN‐A1 Gene
Author(s) -
Sherman J. D.,
Yan L.,
Talbert L.,
Dubcovsky J.
Publication year - 2004
Publication title -
crop science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.76
H-Index - 147
eISSN - 1435-0653
pISSN - 0011-183X
DOI - 10.2135/cropsci2004.1832
Subject(s) - biology , locus (genetics) , vernalization , allele , backcrossing , genetics , genotype , habit , germplasm , gene , genotyping , botany , psychology , psychotherapist
Growth habit varies among accessions of hexaploid wheat ( Triticum aestivum L.). The winter habit genotype (homozygous recessive for vrn‐A1 , vrn‐B1 , vrn‐D1 ) requires a cold treatment to induce flowering and is generally planted in the fall. Spring habit genotypes flower in the absence of a vernalization treatment. Spring habit is conferred by a dominant allele at any of the three VRN‐1 loci, but varieties carrying the VRN‐A1 locus are the most frequent and usually flower earlier. To facilitate selection in populations segregating at the VRN‐A1 locus and to assist in genotyping wheat accessions of unknown VRN‐1 composition, a PCR‐based marker for growth habit would be useful. The VRN‐A1 gene was recently cloned allowing for the development of markers for growth habit. In this report, we designed primer sets specific for the VRN‐A1 locus, and used them to amplify an 810‐bp segment of the VRN‐A1 gene between intron 4 and exon 8 from 40 spring wheat lines and 37 winter wheat lines. Three diagnostic nucleotide changes were identified that differentiated the dominant Vrn‐A1 and recessive vrn‐A1 alleles in 75 out of the 77 genotypes analyzed in this study. One of these differences resulted in the presence of an additional Aci I restriction site in the allele for spring growth habit. This difference was exploited to develop a cleavage amplification polymorphic sequence (CAPS) that can be used to determine the allelic state at VRN‐A1 in germplasm collections, and as a marker in backcross breeding projects. An additional pair of dominant markers was developed from a different polymorphism.