Genome-wide SNP identification and characterization in two soybean cultivars with contrasting mungbean yellow mosaic india virus disease resistance traits

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Abstract

Mungbean yellow mosaic India virus (MYMIV) is a bipartite Geminivirus, which causes severe yield loss in soybean (Glycine max). Considering this, the present study was conducted to develop large-scale genome-wide single nucleotide polymorphism (SNP) markers and identify potential markers linked with known disease resistance loci for their effective use in genomics-assisted breeding to impart durable MYMIV tolerance. The whole-genome resequencing of MYMIV resistant cultivar 'UPSM-534 ' and susceptible Indian cultivar 'JS-335' was performed to identify high-quality SNPs and InDels (insertion and deletions). Approximately 234 and 255 million of 100-bp paired-end reads were generated from UPSM-534 and JS-335, respectively, which provided ∼98%coverage of reference soybean genome. A total of 3083987 SNPs (1559556 in UPSM-534 and 1524431 in JS-335) and 562858 InDels (281958 in UPSM-534 and 280900 in JS-335) were identified. Of these, 1514 SNPs were found to be present in 564 candidate disease resistance genes. Among these, 829 non-synonymous and 671 synonymous SNPs were detected in 266 and 286 defence-related genes, respectively. Noteworthy, a non-synonymous SNP (in chromosome 18, named 18-1861613) at the 149 th base-pair of LEUCINE-RICH REPEAT RECEPTOR-LIKE PROTEIN KINASE gene responsible for a G/C transversion [proline (CCC) to alanine (GCC)] was identified and validated in a set of 12 soybean cultivars. Taken together, the present study generated a large-scale genomic resource such as, SNPs and InDels at a genome-wide scale that will facilitate the dissection of various complex traits through construction of high-density linkage maps and fine mapping. In the present scenario, these markers can be effectively used to design high-density SNP arrays for their large-scale validation and high-throughput genotyping in diverse natural and mapping populations, which could accelerate genomics-assisted MYMIV disease resistance breeding in soybean.

Figures

  • Fig 1. Phenotypic expression of soybean cultivars (a) UPSM-534 [MYMIV tolerant] and (b) JS-335 [MYMIV susceptible] in field conditions.
  • Table 1. Infectivity analysis of MYMIV by agroinoculation in soybean seedling of different cultivars.
  • Table 2. Statistics for high quality reads derived from JS-335 and UPSM-534 which were mapped onto the reference genome of soybean.
  • Fig 2. Comparison of (a) SNP and (b) InDel distributions between both the cultivars (JS-335 and UPSM-534).
  • Fig 3. Frequency of different nucleotides substitution types in the identified SNPs from JS-335 and UPSM-534.
  • Fig 4. Frequency of length distribution of InDels JS-335 and UPSM-534.
  • Fig 5. Number and distribution of (a) SNPs and (b) InDels detected on the soybean chromosomes in both the cultivars (JS-335 and UPSM-534).
  • Fig 6. Density distribution of (a) SNP and (b) InDel in all the 20 chromosomes of soybean. JS-335 (outer circle) and UPSM-534 (inner circle).

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APA

Yadav, C. B., Bhareti, P., Muthamilarasan, M., Mukherjee, M., Khan, Y., Rathi, P., & Prasad, M. (2015). Genome-wide SNP identification and characterization in two soybean cultivars with contrasting mungbean yellow mosaic india virus disease resistance traits. PLoS ONE, 10(4). https://doi.org/10.1371/journal.pone.0123897

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