Genome-Wide Association Analysis Pinpoints Additional Major Genomic Regions Conferring Resistance to Soybean Cyst Nematode ( Ichinohe).

Dung T Tran, Clinton J Steketee, Jeffrey D Boehm, James Noe, Zenglu Li
Author Information
  1. Dung T Tran: Institute of Plant Breeding, Genetics and Genomics and Department of Crop and Soil Sciences, University of Georgia, Athens, GA, United States.
  2. Clinton J Steketee: Institute of Plant Breeding, Genetics and Genomics and Department of Crop and Soil Sciences, University of Georgia, Athens, GA, United States.
  3. Jeffrey D Boehm: Institute of Plant Breeding, Genetics and Genomics and Department of Crop and Soil Sciences, University of Georgia, Athens, GA, United States.
  4. James Noe: Department of Plant Pathology, University of Georgia, Athens, GA, United States.
  5. Zenglu Li: Institute of Plant Breeding, Genetics and Genomics and Department of Crop and Soil Sciences, University of Georgia, Athens, GA, United States.

Abstract

Soybean cyst nematode ( Ichinohe) (SCN) is the most destructive pest affecting soybeans [ (L.) Merr.] in the U.S. To date, only two major SCN resistance alleles, and , identified in PI 88788 () and Peking (), residing on chromosomes (Chr) 18 and 8, respectively, have been widely used to develop SCN resistant cultivars in the U.S. Thus, some SCN populations have evolved to overcome the PI 88788 and Peking derived resistance, making it a priority for breeders to identify new alleles and sources of SCN resistance. Toward that end, 461 soybean accessions from various origins were screened using a greenhouse SCN bioassay and genotyped with Illumina SoySNP50K iSelect BeadChips and three KASP SNP markers developed at the and loci to perform a genome-wide association study (GWAS) and a haplotype analysis at the and loci. In total, 35,820 SNPs were used for GWAS, which identified 12 SNPs at four genomic regions on Chrs 7, 8, 10, and 18 that were significantly associated with SCN resistance ( < 0.001). Of those, three SNPs were located at and , and 24 predicted genes were found near the significant SNPs on Chrs 7 and 10. KASP SNP genotyping results of the 462 accessions at the and loci identified 30 that carried PI 88788-type resistance, 50 that carried Peking-type resistance, and 58 that carried neither the Peking-type nor the PI 88788-type resistance alleles, indicating they may possess novel SCN resistance alleles. By using two subsets of SNPs near the and loci obtained from SoySNP iSelect BeadChips, a haplotype analysis of 461 accessions grouped those 58 accessions differently from the accessions carrying Peking or PI 88788 derived resistance, thereby validating the genotyping results at and . The significant SNPs, candidate genes, and newly characterized SCN resistant accessions will be beneficial for the development of DNA markers to be used for marker-assisted breeding and developing soybean cultivars carrying novel sources of SCN resistance.

Keywords

References

  1. Bioinformatics. 2005 Jan 15;21(2):263-5 [PMID: 15297300]
  2. Theor Appl Genet. 2005 Sep;111(5):965-71 [PMID: 16075207]
  3. Bioinformatics. 2007 Oct 1;23(19):2633-5 [PMID: 17586829]
  4. Theor Appl Genet. 2008 Apr;116(6):777-87 [PMID: 18292984]
  5. Theor Appl Genet. 2009 Apr;118(6):1093-105 [PMID: 19184662]
  6. J Nematol. 2002 Dec;34(4):279-88 [PMID: 19265945]
  7. J Nematol. 1988 Jul;20(3):392-5 [PMID: 19290228]
  8. Theor Appl Genet. 2010 Feb;120(3):633-44 [PMID: 19856174]
  9. Nat Genet. 2010 Apr;42(4):355-60 [PMID: 20208535]
  10. Theor Appl Genet. 2010 Nov;121(7):1253-66 [PMID: 20559815]
  11. Bioinformatics. 2012 Sep 15;28(18):2397-9 [PMID: 22796960]
  12. Science. 2012 Nov 30;338(6111):1206-9 [PMID: 23065905]
  13. Nature. 2012 Dec 13;492(7428):256-60 [PMID: 23235880]
  14. Theor Appl Genet. 2013 Jul;126(7):1825-38 [PMID: 23568221]
  15. Plant Methods. 2013 Jul 22;9:29 [PMID: 23876160]
  16. Theor Appl Genet. 1995 Sep;91(4):574-81 [PMID: 24169883]
  17. Plant Physiol. 2014 Apr 14;165(2):630-647 [PMID: 24733883]
  18. G3 (Bethesda). 2014 Sep 22;4(11):2283-94 [PMID: 25246241]
  19. BMC Genomics. 2015 Apr 18;16:314 [PMID: 25903750]
  20. Mol Breed. 2015;35(6):131 [PMID: 26028986]
  21. BMC Genomics. 2015 Aug 12;16:593 [PMID: 26263897]
  22. BMC Genomics. 2015 Aug 13;16:598 [PMID: 26268218]
  23. Plant Sci. 2016 Jan;242:342-350 [PMID: 26566850]
  24. Phytopathology. 2016 Oct;106(10):1139-1151 [PMID: 27135674]
  25. Front Plant Sci. 2016 Aug 17;7:1214 [PMID: 27582748]
  26. Theor Appl Genet. 2016 Dec;129(12):2295-2311 [PMID: 27796432]
  27. Plant Genome. 2016 Jul;9(2): [PMID: 27898820]
  28. Sci Rep. 2017 Mar 24;7:45226 [PMID: 28338077]
  29. BMC Genomics. 2017 Jun 14;18(1):462 [PMID: 28615053]
  30. Mol Genet Genomics. 2017 Dec;292(6):1257-1265 [PMID: 28710561]
  31. Proc Natl Acad Sci U S A. 2018 May 8;115(19):E4512-E4521 [PMID: 29695628]
  32. Plant Dis. 2007 Nov;91(11):1473-1476 [PMID: 30780744]

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