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长片段序列组装有助于揭示小麦-长穗偃麦草 6VS.6AL 易位染色体的基因组结构和小变异。

Long-range assembly of sequences helps to unravel the genome structure and small variation of the wheat-Haynaldia villosa translocated chromosome 6VS.6AL.

机构信息

National Key Laboratory of Crop Genetics and Germplasm Enhancement, Cytogenetics Institute, Nanjing Agricultural University/JCIC-MCP, Nanjing, China.

Institute of Experimental Botany of the Czech Academy of Sciences, Centre of the Region Haná for Biotechnological and Agricultural Research, Olomouc, Czech Republic.

出版信息

Plant Biotechnol J. 2021 Aug;19(8):1567-1578. doi: 10.1111/pbi.13570. Epub 2021 Mar 1.

DOI:10.1111/pbi.13570
PMID:33606347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8384597/
Abstract

Genomics studies in wild species of wheat have been limited due to the lack of references; however, new technologies and bioinformatics tools have much potential to promote genomic research. The wheat-Haynaldia villosa translocation line T6VS·6AL has been widely used as a backbone parent of wheat breeding in China. Therefore, revealing the genome structure of translocation chromosome 6VS·6AL will clarify how this chromosome formed and will help to determine how it affects agronomic traits. In this study, chromosome flow sorting, NGS sequencing and Chicago long-range linkage assembly were innovatively used to produce the assembled sequences of 6VS·6AL, and gene prediction and genome structure characterization at the molecular level were effectively performed. The analysis discovered that the short arm of 6VS·6AL was actually composed of a large distal segment of 6VS, a small proximal segment of 6AS and the centromere of 6A, while the collinear region in 6VS corresponding to 230-260 Mb of 6AS-Ta was deleted when the recombination between 6VS and 6AS occurred. In addition to the molecular mechanism of the increased grain weight and enhanced spike length produced by the translocation chromosome, it may be correlated with missing GW2-V and an evolved NRT-V cluster. Moreover, a fine physical bin map of 6VS was constructed by the high-throughput developed 6VS-specific InDel markers and a series of newly identified small fragment translocation lines involving 6VS. This study will provide essential information for mining of new alien genes carried by the 6VS·6AL translocation chromosome.

摘要

由于缺乏参考,野生小麦的基因组学研究受到限制;然而,新技术和生物信息学工具具有很大的潜力来促进基因组研究。小麦-长穗偃麦草易位系 T6VS·6AL 已被广泛用作中国小麦育种的骨干亲本。因此,揭示易位染色体 6VS·6AL 的基因组结构将阐明该染色体是如何形成的,并有助于确定它如何影响农艺性状。在这项研究中,创新性地使用染色体流式分选、NGS 测序和芝加哥长程连锁组装技术来生成 6VS·6AL 的组装序列,并有效地进行了基因预测和分子水平的基因组结构特征分析。分析发现,6VS·6AL 的短臂实际上由 6VS 的一个大的远端片段、6AS 的一个小的近端片段和 6A 的着丝粒组成,而当 6VS 和 6AS 之间发生重组时,6AS-Ta 中对应于 230-260 Mb 的 6VS 共线性区域缺失了。除了易位染色体增加粒重和增强穗长的分子机制外,它可能与缺失的 GW2-V 和进化的 NRT-V 簇有关。此外,通过高通量开发的 6VS 特异性 InDel 标记和一系列涉及 6VS 的新鉴定的小片段易位系构建了 6VS 的精细物理 bin 图谱。这项研究将为挖掘 6VS·6AL 易位染色体携带的新外源基因提供重要信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/9f402b585242/PBI-19-1567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/f6214e099c02/PBI-19-1567-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/ab68542779d6/PBI-19-1567-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/273df061c918/PBI-19-1567-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/dec28bef928a/PBI-19-1567-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/7552c2c730cc/PBI-19-1567-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/9f402b585242/PBI-19-1567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/f6214e099c02/PBI-19-1567-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/ab68542779d6/PBI-19-1567-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/273df061c918/PBI-19-1567-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/dec28bef928a/PBI-19-1567-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/7552c2c730cc/PBI-19-1567-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62cf/11386003/9f402b585242/PBI-19-1567-g001.jpg

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