Dissecting the genetic basis of UV-B responsive metabolites in rice

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Feng Zhang, Chenkun Yang, Hao Guo, Yufei Li, Shuangqian Shen, Qianqian Zhou, Chun Li, Chao Wang, Ting Zhai, Lianghuan Qu, Cheng Zhang, Xianqing Liu, Jie Luo, Wei Chen, Shouchuang Wang, Jun Yang, Cui Yu, Yanyan Liu
{"title":"Dissecting the genetic basis of UV-B responsive metabolites in rice","authors":"Feng Zhang, Chenkun Yang, Hao Guo, Yufei Li, Shuangqian Shen, Qianqian Zhou, Chun Li, Chao Wang, Ting Zhai, Lianghuan Qu, Cheng Zhang, Xianqing Liu, Jie Luo, Wei Chen, Shouchuang Wang, Jun Yang, Cui Yu, Yanyan Liu","doi":"10.1186/s13059-024-03372-x","DOIUrl":null,"url":null,"abstract":"UV-B, an important environmental factor, has been shown to affect the yield and quality of rice (Oryza sativa) worldwide. However, the molecular mechanisms underlying the response to UV-B stress remain elusive in rice. We perform comprehensive metabolic profiling of leaves from 160 diverse rice accessions under UV-B and normal light conditions using a widely targeted metabolomics approach. Our results reveal substantial differences in metabolite accumulation between the two major rice subspecies indica and japonica, especially after UV-B treatment, implying the possible role and mechanism of metabolome changes in subspecies differentiation and the stress response. We next conduct a transcriptome analysis from four representative rice varieties under UV-B stress, revealing genes from amino acid and flavonoid pathways involved in the UV-B response. We further perform a metabolite-based genome-wide association study (mGWAS), which reveals 3307 distinct loci under UV-B stress. Identification and functional validation of candidate genes show that OsMYB44 regulates tryptamine accumulation to mediate UV-B tolerance, while OsUVR8 interacts with OsMYB110 to promote flavonoid accumulation and UV-B tolerance in a coordinated manner. Additionally, haplotype analysis suggests that natural variation of OsUVR8groupA contributes to UV-B resistance in rice. Our study reveals the complex biochemical and genetic foundations that govern the metabolite dynamics underlying the response, tolerance, and adaptive strategies of rice to UV-B stress. These findings provide new insights into the biochemical and genetic basis of the metabolome underlying the crop response, tolerance, and adaptation to UV-B stress.","PeriodicalId":12611,"journal":{"name":"Genome Biology","volume":"17 1","pages":""},"PeriodicalIF":10.1000,"publicationDate":"2024-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genome Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s13059-024-03372-x","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

UV-B, an important environmental factor, has been shown to affect the yield and quality of rice (Oryza sativa) worldwide. However, the molecular mechanisms underlying the response to UV-B stress remain elusive in rice. We perform comprehensive metabolic profiling of leaves from 160 diverse rice accessions under UV-B and normal light conditions using a widely targeted metabolomics approach. Our results reveal substantial differences in metabolite accumulation between the two major rice subspecies indica and japonica, especially after UV-B treatment, implying the possible role and mechanism of metabolome changes in subspecies differentiation and the stress response. We next conduct a transcriptome analysis from four representative rice varieties under UV-B stress, revealing genes from amino acid and flavonoid pathways involved in the UV-B response. We further perform a metabolite-based genome-wide association study (mGWAS), which reveals 3307 distinct loci under UV-B stress. Identification and functional validation of candidate genes show that OsMYB44 regulates tryptamine accumulation to mediate UV-B tolerance, while OsUVR8 interacts with OsMYB110 to promote flavonoid accumulation and UV-B tolerance in a coordinated manner. Additionally, haplotype analysis suggests that natural variation of OsUVR8groupA contributes to UV-B resistance in rice. Our study reveals the complex biochemical and genetic foundations that govern the metabolite dynamics underlying the response, tolerance, and adaptive strategies of rice to UV-B stress. These findings provide new insights into the biochemical and genetic basis of the metabolome underlying the crop response, tolerance, and adaptation to UV-B stress.
剖析水稻紫外线-B 反应性代谢物的遗传基础
紫外线-B 作为一种重要的环境因素,已被证明会影响全球水稻(Oryza sativa)的产量和品质。然而,水稻对紫外线-B 胁迫反应的分子机制仍然难以捉摸。我们采用广泛的靶向代谢组学方法,对紫外线-B 和正常光照条件下 160 种不同水稻品种的叶片进行了全面的代谢分析。我们的研究结果表明,籼稻和粳稻这两个主要水稻亚种之间的代谢物积累存在很大差异,尤其是在紫外线-B 处理之后,这意味着代谢组的变化在亚种分化和胁迫响应中可能扮演的角色和机制。接下来,我们对紫外线-B 胁迫下的四个代表性水稻品种进行了转录组分析,揭示了参与紫外线-B 胁迫响应的氨基酸和类黄酮通路基因。我们进一步进行了基于代谢物的全基因组关联研究(mGWAS),发现了紫外线-B 胁迫下的 3307 个不同基因位点。候选基因的鉴定和功能验证表明,OsMYB44调控色胺积累以介导紫外线-B耐受性,而OsUVR8与OsMYB110相互作用,以协调的方式促进类黄酮积累和紫外线-B耐受性。此外,单倍型分析表明,OsUVR8groupA 的自然变异有助于水稻的抗紫外线-B 能力。我们的研究揭示了影响水稻对紫外线-B 胁迫的响应、耐受性和适应策略的代谢动态的复杂生化和遗传基础。这些发现为作物对紫外线-B 胁迫的响应、耐受和适应所依赖的代谢组的生化和遗传基础提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信