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新型小麦-1BS·1EL 易位系抗条锈病的细胞遗传学和基因组特征分析。

Cytogenetic and Genomic Characterization of a Novel Wheat-Tetraploid 1BS⋅1EL Translocation Line with Stripe Rust Resistance.

机构信息

State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China, Sichuan Agricultural University, Chengdu 611130, Sichuan, China.

Triticeae Research Institute, Sichuan Agricultural University, Chengdu 611130, Sichuan, China.

出版信息

Plant Dis. 2024 Jul;108(7):2065-2072. doi: 10.1094/PDIS-12-23-2799-RE. Epub 2024 Jun 24.

Abstract

Stripe rust, caused by f. sp. , is a destructive wheat disease pathogen. is a valuable germplasm including diploid, tetraploid, and decaploid with plenty of biotic and abiotic resistance. In a previous study, we generated a stripe rust-resistant wheat-tetraploid 1E/1D substitution line, K17-841-1. To further apply the wild germplasm for wheat breeding, we selected and obtained a new homozygous wheat-tetraploid translocation line, T1BS⋅1EL, using genomic in situ hybridization, fluorescence in situ hybridization (FISH), oligo-FISH painting, and the wheat 55K single nucleotide polymorphism genotyping array. The T1BS⋅1EL is highly resistant to stripe rust at the seedling and adult stages. Pedigree and molecular marker analyses revealed that the resistance gene was located on the chromosome arm 1EL of tetraploid . tentatively named . In addition, we developed and validated 32 simple sequence repeat markers and two kompetitive allele-specific PCR assays that were specific to the tetraploid chromosome arm 1EL to facilitate marker-assisted selection for alien 1EL stripe rust resistance breeding. This will help us explore and locate the stripe rust resistance gene mapping on the 1E chromosome and deploy it in the wheat breeding program.

摘要

条锈病,由 f. sp. 引起,是一种破坏性的小麦病害病原体。 是一种有价值的种质资源,包括二倍体、四倍体和十倍体,具有丰富的生物和非生物抗性。在之前的研究中,我们生成了一个抗条锈病的小麦-四倍体 1E/1D 替换系,K17-841-1。为了进一步将野生种质应用于小麦育种,我们使用基因组原位杂交、荧光原位杂交(FISH)、寡核苷酸 FISH 染色和小麦 55K 单核苷酸多态性基因分型阵列,选择并获得了一个新的纯合小麦-四倍体 1BS⋅1EL 易位系。T1BS⋅1EL 在幼苗和成株期对条锈病高度抗性。系谱和分子标记分析表明,抗性基因位于四倍体 的 1EL 染色体臂上,我们暂将其命名为 。此外,我们开发并验证了 32 个简单序列重复标记和两个针对四倍体 1EL 染色体臂的竞争性等位基因特异性 PCR 检测方法,以促进用于外源 1EL 条锈病抗性育种的标记辅助选择。这将有助于我们探索和定位 1E 染色体上的条锈病抗性基因,并将其部署到小麦育种计划中。

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