QTL mapping and genome-wide association analysis reveal genetic loci and candidate gene for resistance to gray leaf spot in tropical and subtropical maize germplasm
Key message Using QTL mapping and GWAS, two candidate genes ( Zm00001d051039 and Zm00001d051147 ) were consistently identified across the three different environments and BLUP values. GWAS analysis identified the candidate gene, Zm00001d044845 . These genes were subsequently validated to exhibit a s...
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Veröffentlicht in: | Theoretical and applied genetics 2024-12, Vol.137 (12), p.266, Article 266 |
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Sprache: | eng |
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Using QTL mapping and GWAS, two candidate genes (
Zm00001d051039 and Zm00001d051147
) were consistently identified across the three different environments and BLUP values. GWAS analysis identified the candidate gene,
Zm00001d044845
. These genes were subsequently validated to exhibit a significant association with maize gray leaf spot (GLS) resistance.
Gray leaf spot (GLS) is a major foliar disease of maize (
Zea mays
L.) that causes significant yield losses worldwide. Understanding the genetic mechanisms underlying gray leaf spot resistance is crucial for breeding high-yielding and disease-resistant varieties. In this study, eight tropical and subtropical germplasms were crossed with the temperate germplasm Ye107 to develop a nested association mapping (NAM) population comprising 1,653 F2:8 RILs, consisting of eight recombinant inbred line (RIL) subpopulations, using the single-seed descent method. The NAM population was evaluated for GLS resistance in three different environments, and genotyping by sequencing of the NAM population generated 593,719 high-quality single-nucleotide polymorphisms (SNPs). Linkage analysis and genome-wide association studies (GWASs) were conducted to identify candidate genes regulating GLS resistance in maize. Both analyses identified 25 QTLs and 149 SNPs that were significantly associated with GLS resistance. Candidate genes were screened 20 Kb upstream and downstream of the significant SNPs, and three novel candidate genes (
Zm00001d051039
,
Zm00001d051147
, and
Zm00001d044845
) were identified.
Zm00001d051039
and
Zm00001d051147
were located on chromosome 4 and co-localized in both linkage (
qGLS4-1
and
qGLS4-2
) and GWAS analyses. SNP-138,153,206 was located 0.499 kb downstream of the candidate gene
Zm00001d051039
, which encodes the protein IN2-1 homolog B, a homolog of glutathione S-transferase (GST). GSTs and protein IN2-1 homolog B scavenge reactive oxygen species under various stress conditions, and GSTs are believed to protect plants from a wide range of biotic and abiotic stresses by detoxifying reactive electrophilic compounds.
Zm00001d051147
encodes a probable beta-1,4-xylosyltransferase involved in the biosynthesis of xylan in the cell wall, enhancing resistance.
SNP-145,813,215
was located 2.69 kb downstream of the candidate gene.
SNP-5,043,412
was consistently identified in three different environments and BLUP values and was located 8.788 kb downstream of the candidate gene
Zm00001d044845
on chromos |
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ISSN: | 0040-5752 1432-2242 1432-2242 |
DOI: | 10.1007/s00122-024-04764-0 |