About Us | Help Videos | Contact Us | Subscriptions
 

The Plant Genome Abstract - Original Research

SNP Discovery and QTL Mapping of Sclerotinia Basal Stalk Rot Resistance in Sunflower using Genotyping-by-Sequencing

 

This article in TPG

  1. Vol. 9 No. 3
    unlockOPEN ACCESS
     
    Received: Mar 30, 2016
    Accepted: July 19, 2016
    Published: September 29, 2016


    * Corresponding author(s): lili.qi@ars.usda.gov
 View
 Download
 Alerts
 Permissions
Request Permissions
 Share

doi:10.3835/plantgenome2016.03.0035
  1. Zahirul I. Talukdera,
  2. Gerald J. Seilerb,
  3. Qijian Songc,
  4. Guojia Mad and
  5. Lili Qi *b
  1. a Dep. of Plant Sciences, 166 Loftsgard Hall, North Dakota State Univ., Fargo, ND 58102, USA
    b USDA–ARS, Sunflower and Plant Biology Research Unit, Northern Crop Science Laboratory, 1307 18th St. N., Fargo, ND 58102, USA
    c USDA–ARS, Soybean Genomics and Improvement Laboratory, 10300 Baltimore Ave., Beltsville, MD 20705, USA
    d Dep. of Plant Pathology, 306 Walster Hall, North Dakota State Univ., Fargo, ND 58102, USA

Abstract

Basal stalk rot (BSR), caused by the ascomycete fungus Sclerotinia sclerotiorum (Lib.) de Bary, is a serious disease of sunflower (Helianthus annuus L.) in the cool and humid production areas of the world. Quantitative trait loci (QTL) for BSR resistance were identified in a sunflower recombinant inbred line (RIL) population derived from the cross HA 441 × RHA 439. A genotyping-by-sequencing (GBS) approach was adapted to discover single nucleotide polymorphism (SNP) markers. A genetic linkage map was developed comprised of 1053 SNP markers on 17 linkage groups (LGs) spanning 1401.36 cM. The RILs were tested in five environments (locations and years) for resistance to BSR. Quantitative trait loci were identified in each environment separately and also with integrated data across environments. A total of six QTL were identified in all five environments: one of each on LGs 4, 9, 10, 11, 16, and 17. The most significant QTL, Qbsr-10.1 and Qbsr-17.1, were identified at multiple environments on LGs 10 and 17, explaining 31.6 and 20.2% of the observed phenotypic variance, respectively. The remaining four QTL, Qbsr-4.1, Qbsr-9.1, Qbsr-11.1, and Qbsr-16.1, were detected in only one environment on LGs 4, 9, 11, and 16, respectively. Each of these QTL explains between 6.4 and 10.5% of the observed phenotypic variation in the RIL population. Alleles conferring increased resistance were contributed by both parents. The potential of the Qbsr-10.1 and Qbsr-17.1 in marker-assisted selection (MAS) breeding are discussed.

  Please view the pdf by using the Full Text (PDF) link under 'View' to the left.

Copyright © 2016. Copyright © 2016 Crop Science Society of America