New insights into the cold tolerance of upland switchgrass by integrating a haplotype-resolved genome and multi-omics analysis

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Bingchao Wu, Dan Luo, Yuesen Yue, Haidong Yan, Min He, Xixi Ma, Bingyu Zhao, Bin Xu, Jie Zhu, Jing Wang, Jiyuan Jia, Min Sun, Zheni Xie, Xiaoshan Wang, Linkai Huang
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Abstract

Switchgrass (Panicum virgatum L.) is a bioenergy and forage crop. Upland switchgrass exhibits superior cold tolerance compared to the lowland ecotype, but the underlying molecular mechanisms remain unclear. Here, we present a high-quality haplotype-resolved genome of the upland ecotype “Jingji31.” We then conduct multi-omics analysis to explore the mechanism underlying its cold tolerance. By comparative transcriptome analysis of the upland and lowland ecotypes, we identify many genes with ecotype-specific differential expression, particularly members of the cold-responsive (COR) gene family, under cold stress. Notably, AFB1, ATL80, HOS10, and STRS2 gene families show opposite expression changes between the two ecotypes. Based on the haplotype-resolved genome of “Jingji31,” we detect more cold-induced allele-specific expression genes in the upland ecotype than in the lowland ecotype, and these genes are significantly enriched in the COR gene family. By genome-wide association study, we detect an association signal related to the overwintering rate, which overlaps with a selective sweep region containing a cytochrome P450 gene highly expressed under cold stress. Heterologous overexpression of this gene in rice alleviates leaf chlorosis and wilting under cold stress. We also verify that expression of this gene is suppressed by a structural variation in the promoter region. Based on the high-quality haplotype-resolved genome and multi-omics analysis of upland switchgrass, we characterize candidate genes responsible for cold tolerance. This study advances our understanding of plant cold tolerance, which provides crop breeding for improved cold tolerance.
整合单倍型解决基因组和多组学分析对山地柳枝稷耐寒性的新见解
柳枝稷(Panicum virgatum L.)是一种生物能源和饲料作物。与低地生态型相比,山地柳枝稷表现出更强的耐寒性,但其分子机制尚不清楚。在这里,我们提出了一个高质量的单倍型解决基因组的山地生态型“京吉31”。然后,我们进行了多组学分析,以探索其耐寒性的机制。通过比较高原和低地生态型的转录组分析,我们发现了许多在寒冷胁迫下具有生态型特异性差异表达的基因,特别是冷响应(COR)基因家族的成员。值得注意的是,AFB1、ATL80、HOS10和STRS2基因家族在两种生态型中表现出相反的表达变化。基于“京鸡31”的单倍型解析基因组,我们在旱地生态型中检测到比低地生态型更多的冷诱导等位基因特异性表达基因,这些基因在COR基因家族中显著富集。通过全基因组关联研究,我们发现了一个与越冬率相关的关联信号,该信号与冷胁迫下高表达的细胞色素P450基因的选择性扫描区域重叠。该基因在水稻中外源过表达可缓解冷胁迫下的叶片萎黄和萎蔫。我们还证实该基因的表达受到启动子区域结构变化的抑制。基于高质量的单倍型解析基因组和多组学分析,我们对旱地柳枝稷耐寒性候选基因进行了表征。该研究为我们进一步了解植物的耐寒性提供了理论依据,为作物的耐寒性育种提供了理论依据。
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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