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对一个家系的核心品系进行重测序,鉴定了棉花改良过程中基因组片段的来源和关键农艺性状位点。

Resequencing core accessions of a pedigree identifies derivation of genomic segments and key agronomic trait loci during cotton improvement.

机构信息

State Key Laboratory of Cotton Biology, Institute of Cotton Research, Chinese Academy of Agricultural Sciences, Anyang, China.

Key Laboratory of the Ministry of Education for Medicinal Plant Resources and Natural Pharmaceutical Chemistry, National Engineering Laboratory for Resource Development of Endangered Crude Drugs in the Northwest of China, College of Life Sciences, Shaanxi Normal University, Xi'an, China.

出版信息

Plant Biotechnol J. 2019 Apr;17(4):762-775. doi: 10.1111/pbi.13013. Epub 2018 Oct 18.

DOI:10.1111/pbi.13013
PMID:30220108
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6419577/
Abstract

Upland cotton (Gossypium hirsutum) is the world's largest source of natural fibre and dominates the global textile industry. Hybrid cotton varieties exhibit strong heterosis that confers high fibre yields, yet the genome-wide effects of artificial selection that have influenced Upland cotton during its breeding history are poorly understood. Here, we resequenced Upland cotton genomes and constructed a variation map of an intact breeding pedigree comprising seven elite and 19 backbone parents. Compared to wild accessions, the 26 pedigree accessions underwent strong artificial selection during domestication that has resulted in reduced genetic diversity but stronger linkage disequilibrium and higher extents of selective sweeps. In contrast to the backbone parents, the elite parents have acquired significantly improved agronomic traits, with an especially pronounced increase in the lint percentage. Notably, identify by descent (IBD) tracking revealed that the elite parents inherited abundant beneficial trait segments and loci from the backbone parents and our combined analyses led to the identification of a core genomic segment which was inherited in the elite lines from the parents Zhong 7263 and Ejing 1 and that was strongly associated with lint percentage. Additionally, SNP correlation analysis of this core segment showed that a non-synonymous SNP (A-to-G) site in a gene encoding the cell wall-associated receptor-like kinase 3 (GhWAKL3) protein was highly correlated with increased lint percentage. Our results substantially increase the valuable genomics resources available for future genetic and functional genomics studies of cotton and reveal insights that will facilitate yield increases in the molecular breeding of cotton.

摘要

陆地棉(Gossypium hirsutum)是世界上最大的天然纤维来源,主导着全球纺织业。杂交棉品种表现出强大的杂种优势,从而提高了纤维产量,但在棉花的选育历史中,人工选择对其基因组的广泛影响仍知之甚少。在这里,我们对陆地棉基因组进行了重测序,并构建了一个完整的育种系谱的变异图谱,该系谱由 7 个优良品种和 19 个骨干亲本组成。与野生品种相比,这 26 个系谱品种在驯化过程中经历了强烈的人工选择,导致遗传多样性减少,但连锁不平衡增强,选择清除程度更高。与骨干亲本相比,优良亲本获得了明显改善的农艺性状,尤其是皮棉率显著提高。值得注意的是,通过血统鉴定(IBD)追踪发现,优良亲本从骨干亲本中继承了丰富的有益性状片段和位点,我们的综合分析确定了一个核心基因组片段,该片段在从中兴 7263 和额景 1 亲本的优良系中被继承,并与皮棉率呈强烈相关。此外,对该核心片段的 SNP 相关性分析表明,编码细胞壁相关受体样激酶 3(GhWAKL3)蛋白的基因中的一个非同义 SNP(A 到 G)位点与皮棉率的增加高度相关。我们的研究结果大大增加了棉花未来遗传和功能基因组学研究的宝贵基因组资源,并揭示了有助于提高棉花分子育种产量的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/f9143d508a04/PBI-17-762-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/a5fa1b42a1f1/PBI-17-762-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/f1106215f305/PBI-17-762-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/1c8ac83adccb/PBI-17-762-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/997ed4339116/PBI-17-762-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/c0ccb6d5ce40/PBI-17-762-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/f9143d508a04/PBI-17-762-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/a5fa1b42a1f1/PBI-17-762-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/f1106215f305/PBI-17-762-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/1c8ac83adccb/PBI-17-762-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/997ed4339116/PBI-17-762-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/c0ccb6d5ce40/PBI-17-762-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/964e/11386894/f9143d508a04/PBI-17-762-g003.jpg

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