Nested-Association Mapping (NAM) Based Genetic Dissection Reveals Candidate QTLs and Genes for Ear-Kernel Related Traits in Maize

Jiang, Fuyan; Bi, Yaqi; Jing, Xin; Wang, Tianyi; Yin, Yingfu; Yao, Wenhua; Fan, Xingming

doi:10.2139/ssrn.4193808

Cited by 1 publication

(1 citation statement)

References 48 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…"Repj" denotes the effect of the jth replication, while "εijlk" signi es random effects. Additionally, '(Line×Loc)ij' represents the interaction between the ith line and jth location, and 'Rep (Loc)jl' indicates the effect of the ith replication at the jth location (Jiang et al 2023).…”

Section: Experimental Materialsmentioning

confidence: 99%

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

Pan,

Jiang,

Shaw

et al. 2024

Preprint

View full text Add to dashboard Cite

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 four 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 (GWAS) 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 20Kb 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 0.499kb downstream of the candidate gene Zm00001d051039, which encodes the protein IN2-1 homolog B, a homolog of glutathione S-transferase (GSTs). GSTs and Protein IN2-1 homolog B scavenge reactive oxygen species (ROS) 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 four different environments and was located 8.788 kb downstream of the candidate gene Zm00001d044845 on chromosome 9. Zm00001d044845 encodes the U-box domain-containing protein 4 (PUB4), which is involved in regulating plant immunity. The findings of this study are significant for marker-assisted breeding aimed at enhancing resistance to GLS in maize and laying the foundation for further elucidation of the genetic mechanisms underlying resistance to gray leaf spot in maize and breeding of new disease-resistant varieties.

show abstract

Section: Experimental Materialsmentioning

confidence: 99%