| Autor: |
Kumar B; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Choudhary M; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Kumar P; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Kumar K; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Kumar S; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Singh BK; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Lahkar C; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Meenakshi; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Kumar P; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India., Dar ZA; Dryland Agriculture Research Station, SKUAST-K, Srinagar 190001, India., Devlash R; CSKHPKV, HAREC, Bajaura 175125, India., Hooda KS; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India.; ICAR-National Bureau of Plant Genetic Resources, New Delhi 110012, India., Guleria SK; CSKHPKV, HAREC, Bajaura 175125, India., Rakshit S; ICAR-Indian Institute of Maize Research, Ludhiana 141004, India. |
| Abstrakt: |
Maize is an important cereal crop in the world for feed, food, fodder, and raw materials of industries. Turcicum leaf blight (TLB) is a major foliar disease that can cause more than 50% yield losses in maize. Considering this, the molecular diversity, population structure, and genome-wide association study (GWAS) for TLB resistance were studied in 288 diverse inbred lines genotyped using 89 polymorphic simple sequence repeats (SSR) markers. These lines werescreened for TLB disease at two hot-spot locations under artificially inoculated conditions. The average percent disease incidence (PDI) calculated for each genotype ranged from 17 (UMI 1201) to 78% (IML 12-22) with an overall mean of 40%. The numbers of alleles detected at a locus ranged from twoto nine, with a total of 388 alleles. The polymorphic information content (PIC) of each marker ranged between 0.04 and 0.86. Out of 89 markers, 47 markers were highly polymorphic (PIC ≥ 0.60). This indicated that the SSR markers used were very informative and suitable for genetic diversity, population structure, and marker-trait association studies.The overall observed homozygosity for highly polymorphic markers was 0.98, which indicated that lines used were genetically pure. Neighbor-joining clustering, factorial analysis, and population structure studies clustered the 288 lines into 3-5 groups. The patterns of grouping were in agreement with the origin and pedigree records of the genotypesto a greater extent.A total of 94.10% lines were successfully assigned to one or another group at a membership probability of ≥0.60. An analysis of molecular variance (AMOVA) revealed highly significant differences among populations and within individuals. Linkage disequilibrium for r 2 and D' between loci ranged from 0 to 0.77 and 0 to 1, respectively. A marker trait association analysis carried out using a general linear model (GLM) and mixed linear model (MLM), identified 15 SSRs markers significantly associated with TLB resistance.These 15 markers were located on almost all chromosomes (Chr) except 7, 8, and 9. The phenotypic variation explained by these loci ranged from 6% (umc1367) to 26% (nc130, phi085). Maximum 7 associated markers were located together on Chr 2 and 5. The selected regions identified on Chr 2 and 5 corroborated the previous studies carried out in the Indian maize germplasm. Further, 11 candidate genes were identified to be associated with significant markers. The identified sources for TLB resistance and associated markers may be utilized in molecular breeding for the development of suitable genotypes. |
