Nottingham BBSRC Wheat Research Centre, Division of Plant and Crop Sciences, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, UK.
Molecular Breeding Department, Agricultural Institute, Centre for Agricultural Research, Hungarian Academy of Sciences, Martonvásár, Hungary.
Theor Appl Genet. 2019 May;132(5):1555-1570. doi: 10.1007/s00122-019-03300-9. Epub 2019 Feb 14.
Cytogenetic analysis and array-based SNP genotyping of wheat- Th. intermedium introgression lines allowed identification of 634 chromosome-specific SNP markers across all twenty-one chromosomes of Th. intermedium (StJ J , 2 n = 6 x = 42). Thinopyrum intermedium (2n = 6x = 42, StJJ) is one of the most promising reservoirs of useful genes including tolerance to abiotic stresses, perenniality and disease resistance not available in the cultivated bread wheat. The transfer of genetic diversity from wild species to wheat offers valuable responses to the effects of climate change. The new array-based single-nucleotide polymorphism (SNP) marker technology provides cheap and easy-to-use molecular markers for marker-assisted selection (MAS) in wheat breeding programmes. Here, we focus on the generation of a new chromosome-specific SNP marker set that can be used to characterize and identify the Th. intermedium chromosomes or chromosome segments transferred into wheat. A progressive investigation of marker development was conducted using 187 various newly developed wheat-Th. intermedium introgression lines and the Axiom Wheat-Relative Genotyping array. We employed molecular cytogenetic techniques to clarify the genome constitution of the Th. intermedium parental lines and validated 634 chromosome-specific SNPs. Our data confirmed the allohexaploid nature of Th. intermedium and demonstrated that the St genome-specific GISH signal and markers are present at the centromeric regions of chromosomes 1J, 2J, 3J and 7J. The SNP markers presented here will be introduced into current wheat improvement programmes, offering a significant speed-up in wheat breeding and making it possible to deal with the transfer of the full genetic potential of Th. intermedium into wheat.
小麦-中间偃麦草渗入系的细胞遗传学分析和基于阵列的 SNP 基因分型鉴定了中间偃麦草的 21 条染色体上的 634 个染色体特异性 SNP 标记(StJ J ,2n = 6x = 42)。中间偃麦草(2n = 6x = 42,StJJ)是最有前途的基因库之一,其中包括对非生物胁迫、多年生性和抗病性的耐受性,而这些特性在栽培小麦中是没有的。从野生物种向小麦转移遗传多样性为应对气候变化的影响提供了有价值的反应。新的基于阵列的单核苷酸多态性(SNP)标记技术为小麦育种计划中的标记辅助选择(MAS)提供了廉价且易于使用的分子标记。在这里,我们专注于生成一组新的染色体特异性 SNP 标记,可用于描述和鉴定转移到小麦中的中间偃麦草染色体或染色体片段。使用 187 种不同的新开发的小麦-中间偃麦草渗入系和 Axiom Wheat-Relative Genotyping 阵列,逐步进行了标记开发的研究。我们采用分子细胞遗传学技术阐明了中间偃麦草亲本系的基因组组成,并验证了 634 个染色体特异性 SNP。我们的数据证实了中间偃麦草的异源六倍体性质,并表明 St 基因组特异性 GISH 信号和标记存在于染色体 1J、2J、3J 和 7J 的着丝粒区域。这里提出的 SNP 标记将被引入到当前的小麦改良计划中,这将大大加快小麦的育种速度,并使中间偃麦草的全部遗传潜力转移到小麦中成为可能。