高分辨率遗传和物理图谱显示,在A01染色体上的一个重组冷点上,发现了一个花生斑点枯萎病对番茄斑点枯萎病毒(TSWV)的抗性位点PSWDR-1。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2025-03-06 DOI:10.1186/s12864-025-11366-7
Dongliang Wu, Chuanzhi Zhao, Walid Korani, Ethan A Thompson, Hui Wang, Gaurav Agarwal, Jake C Fountain, Albert Culbreath, C Corley Holbrook, Xingjun Wang, Josh P Clevenger, Baozhu Guo
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引用次数: 0

摘要

背景:花生(arachhis hypogaea L.)是一种重要的全球作物,经常受到非生物和生物胁迫的威胁。其中最具破坏性的生物胁迫是番茄斑点枯萎病毒(TSWV),它引起花生斑点枯萎病,造成严重的产量损失。培育抗tswv的品种是新品种释放的关键。先前的研究使用了SunOleic 97R和NC94022衍生的“S”重组自交系(RIL)群体的一个亚群,并确定了抗TSWV的数量性状位点(qtl)。这些研究利用不同的基因分型技术,在A01染色体上发现了大量一致的基因组区域。本研究的目的是利用352个ril的全群体和高密度、高质量的花生SNP阵列,精细定位QTL并鉴定候选基因。结果:我们使用了具有5年疾病评级的两种版本的花生SNP阵列,并成功定位了长期寻找的花生斑点枯萎病抗性位点PSWDR-1。利用花生A01染色体Axiom_Arachis-v1和Axiom_Arachis-v2 SNP阵列进行QTL分析,鉴定出两个主要QTL,分别在3.6 cM和0.28 cM区间内解释41.43%和43.69%的表型变异。这些qtl对应295 kb和235 kb的物理间隔。这两个qtl的唯一重叠区域为488kb。与参考基因组的遗传连锁图谱比较,发现一个1.3 Mb的重组“冷点”(11.325 ~ 12.646 Mb),只有两个il - s1和il - s17的重组事件,表现出不同的表型。这两个重组体的测序证实了冷点,在该区域仅检测到5个snp。结论:本研究成功鉴定了花生斑点病抗性位点PSWDR-1,该位点位于重组“冷点”A01染色体上。PSWDR-1位点包含三个候选基因,一个TIR-NBS-LRR基因(Arahy.1PK53M),一个谷氨酸受体样基因(Arahy.RI1BYW)和一个mlo样蛋白(Arahy.FX71XI)。研究结果为进一步研究候选基因在花生tswv抗性中的作用及在花生tswv抗性育种中的应用奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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High-resolution genetic and physical mapping reveals a peanut spotted wilt disease resistance locus, PSWDR-1, to Tomato spotted wilt virus (TSWV), within a recombination cold-spot on chromosome A01.

Background: Peanut (Arachis hypogaea L.) is a vital global crop, frequently threatened by both abiotic and biotic stresses. Among the most damaging biotic stresses is Tomato spotted wilt virus (TSWV), which causes peanut spotted wilt disease resulting in significant yield loss. Developing TSWV-resistant cultivars is crucial to new cultivar release. Previous studies have used a subset of the "S" recombinant inbred line (RIL) population derived from SunOleic 97R and NC94022 and identified quantitative trait loci (QTLs) for resistance to TSWV. These studies utilized different genotyping techniques and found large consistent genomic regions on chromosome A01. The objective of this study was to fine map the QTL and identify candidate genes using the entire population of 352 RILs and high-density, high-quality peanut SNP arrays.

Results: We used both versions of the peanut SNP arrays with five years of disease ratings, and successfully mapped the long-sought peanut spotted wilt disease resistance locus, PSWDR-1. QTL analyses identified two major QTLs, explaining 41.43% and 43.69% of the phenotypic variance within 3.6 cM and 0.28 cM intervals using the peanut Axiom_Arachis-v1 and Axiom_Arachis-v2 SNP arrays, respectively, on chromosome A01. These QTLs corresponded to 295 kb and 235 kb physical intervals. The unique overlap region of these two QTLs was 488 kb. A comparison of the genetic linkage map with the reference genome revealed a 1.3 Mb recombination "cold spot" (11.325-12.646 Mb) with only two recombination events of RIL-S1 and RIL-S17, which displayed contrasting phenotypes. Sequencing of these two recombinants confirmed the cold spot with only five SNPs detected within this region.

Conclusions: This study successfully identified a peanut spotted wilt disease resistance locus, PSWDR-1, on chromosome A01 within a recombination "cold spot". The PSWDR-1 locus contains three candidate genes, a TIR-NBS-LRR gene (Arahy.1PK53M), a glutamate receptor-like gene (Arahy.RI1BYW), and an MLO-like protein (Arahy.FX71XI). These findings provide a foundation for future functional studies to validate the roles of these candidate genes in resistance and application in breeding TSWV-resistant peanut cultivars.

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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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