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两个对绿豆黄花叶印度病毒病具有不同抗性性状的大豆品种的全基因组单核苷酸多态性鉴定与特征分析

Genome-wide SNP identification and characterization in two soybean cultivars with contrasting Mungbean Yellow Mosaic India Virus disease resistance traits.

作者信息

Yadav Chandra Bhan, Bhareti Priyanka, Muthamilarasan Mehanathan, Mukherjee Minakshi, Khan Yusuf, Rathi Pushpendra, Prasad Manoj

机构信息

National Institute of Plant Genome Research, New Delhi, India.

Department of Genetics and Plant Breeding, Govind Ballabh Pant University of Agriculture and Technology, Pantnagar, Uttarakhand, India.

出版信息

PLoS One. 2015 Apr 13;10(4):e0123897. doi: 10.1371/journal.pone.0123897. eCollection 2015.

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 re-sequencing 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 149th 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.

摘要

绿豆黄花叶印度病毒(MYMIV)是一种双分体双生病毒,可导致大豆(Glycine max)严重减产。鉴于此,本研究旨在开发大规模全基因组单核苷酸多态性(SNP)标记,并鉴定与已知抗病基因座相关的潜在标记,以便在基因组辅助育种中有效利用,赋予大豆持久的MYMIV耐受性。对MYMIV抗性品种‘UPSM-534’和感病印度品种‘JS-335’进行全基因组重测序,以鉴定高质量的SNP和插入缺失(InDels,即插入和缺失)。分别从‘UPSM-534’和‘JS-335’产生了约2.34亿和2.55亿条100碱基对的双端 reads,覆盖了参考大豆基因组约98%的区域。共鉴定出3083987个SNP(‘UPSM-534’中有1559556个,‘JS-335’中有1524431个)和562858个InDels(‘UPSM-534’中有281958个,‘JS-335’中有280900个)。其中,1514个SNP存在于564个候选抗病基因中。其中,在266个和286个防御相关基因中分别检测到829个非同义SNP和671个同义SNP。值得注意的是,在富含亮氨酸重复序列的类受体蛋白激酶基因的第149个碱基对处(位于18号染色体上,命名为18-1861613)鉴定出一个导致G/C转换[脯氨酸(CCC)变为丙氨酸(GCC)]的非同义SNP,并在一组12个大豆品种中得到验证。综上所述,本研究在全基因组范围内产生了如SNP和InDels等大规模基因组资源,这将有助于通过构建高密度连锁图谱和精细定位来剖析各种复杂性状。在当前情况下,这些标记可有效地用于设计高密度SNP阵列,以便在不同的自然群体和作图群体中进行大规模验证和高通量基因分型,从而加速大豆基因组辅助MYMIV抗病育种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/776f/4395324/848cb056856e/pone.0123897.g001.jpg

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