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利用 BSR-seq 对辣椒中宽叶豌豆萎蔫病毒 2 抗性基因 bwvr 进行分子作图。

Molecular mapping of the broad bean wilt virus 2 resistance locus bwvr in Capsicum annuum using BSR-seq.

机构信息

Interdisciplinary Program in Agricultural Biotechnology, College of Agriculture and Life Sciences, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul, 08826, Republic of Korea.

Department of Plant Science and Plant Genomics and Breeding Institute, College of Agriculture and Life Sciences, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul, 08826, Republic of Korea.

出版信息

Theor Appl Genet. 2024 Apr 8;137(5):97. doi: 10.1007/s00122-024-04603-2.

Abstract

Bulked segregant RNA seq of pools of pepper accessions that are susceptible or resistant to Broad bean wilt virus 2 identifies a gene that might confer resistance to this devastating pathogen. The single-stranded positive-sense RNA virus Broad bean wilt virus 2 (BBWV2) causes substantial damage to pepper (Capsicum annuum) cultivation. Here, we describe mapping the BBWV2 resistance locus bwvr using a F recombinant inbred line (RIL) population constructed by crossing the BBWV2-resistant pepper accession 'SNU-C' with the susceptible pepper accession 'ECW30R.' All F plants infected with the BBWV2 strain PAP1 were susceptible to the virus, and the RIL population showed a 1:1 ratio of resistance to susceptibility, indicating that this trait is controlled by a single recessive gene. To map bwvr, we performed bulked segregant RNA-seq (BSR-seq). We sequenced pools of resistant and susceptible lines from the RILs and aligned the reads to the high-quality 'Dempsey' reference genome to identify variants between the pools. This analysis identified 519,887 variants and selected the region from 245.9-250.8 Mb of the Dempsey reference genome as the quantitative trait locus region for bwvr. To finely map bwvr, we used newly designed high-resolution melting (HRM) and Kompetitive allele specific PCR (KASP) markers based on variants obtained from the BSR-seq reads and the PepperSNP16K array. Comparative analysis identified 11 SNU-C-specific SNPs within the bwvr locus. Using markers derived from these variants, we mapped the candidate bwvr locus to the region from 246.833-246.949 kb. SNU-C-specific variants clustered near DEM.v1.00035533 within the bwvr locus. DEM.v1.00035533 encodes the nitrate transporter NPF1.2 and contains a SNP within its 5' untranslated region. The bwvr locus, which contains four genes including DEM.v1.00035533, could represent a valuable resource for global pepper breeding programs.

摘要

对易感性和抗广谱豆萎病毒 2 的辣椒品系群体的分离物进行 bulked segregant RNA 测序,鉴定出一个可能赋予该破坏性病原体抗性的基因。单链正链 RNA 病毒广谱豆萎病毒 2(BBWV2)对辣椒(Capsicum annuum)种植造成了严重损害。在这里,我们通过杂交抗 BBWV2 的辣椒品系“SNU-C”与易感辣椒品系“ECW30R”构建的 F 重组自交系(RIL)群体,描述了 BBWV2 抗性基因 bwvr 的定位。所有用 BBWV2 株 PAP1 感染的 F 植株均对该病毒敏感,而 RIL 群体显示出抗性与易感性的 1:1 比例,表明该性状由单个隐性基因控制。为了定位 bwvr,我们进行了 bulked segregant RNA-seq(BSR-seq)。我们对 RIL 中抗感品系的群体进行测序,并将读取序列与高质量的“Dempsey”参考基因组进行比对,以鉴定群体间的变异。该分析鉴定了 519,887 个变体,并选择 Dempsey 参考基因组的 245.9-250.8 Mb 区域作为 bwvr 的数量性状基因座区域。为了精细定位 bwvr,我们使用基于从 BSR-seq 读取和 PepperSNP16K 阵列获得的变体新设计的高分辨率熔解(HRM)和竞争性等位基因特异性 PCR(KASP)标记。比较分析在 bwvr 基因座内鉴定了 11 个 SNU-C 特异性 SNP。使用源自这些变体的标记,我们将候选 bwvr 基因座映射到 246.833-246.949 kb 区域。SNU-C 特异性变体在 bwvr 基因座内聚集在 DEM.v1.00035533 附近。DEM.v1.00035533 编码硝酸盐转运蛋白 NPF1.2,其 5'非翻译区包含一个 SNP。包含 DEM.v1.00035533 在内的四个基因的 bwvr 基因座可能代表全球辣椒育种计划的宝贵资源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ade2/11001752/2fd708e904c6/122_2024_4603_Fig1_HTML.jpg

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