剖析 mRNA m6A 甲基化增加在甜叶菊自四倍体化中的作用

IF 3.5 3区 生物学 Q1 PLANT SCIENCES
Juan Liu, Mingpu Tan, Yingying Zhang, Jie Zhao, Huijie Liu, Peng Liu, Wenna Meng, Anping Ding, Zengxu Xiang, Mingjia Chen
{"title":"剖析 mRNA m6A 甲基化增加在甜叶菊自四倍体化中的作用","authors":"Juan Liu, Mingpu Tan, Yingying Zhang, Jie Zhao, Huijie Liu, Peng Liu, Wenna Meng, Anping Ding, Zengxu Xiang, Mingjia Chen","doi":"10.1007/s10725-024-01199-x","DOIUrl":null,"url":null,"abstract":"<p>N6-methyladenosine (m<sup>6</sup>A) is the most abundant modification in eukaryotic mRNA. m<sup>6</sup>A functions in embryo development, flowering time regulation, and fruit ripening. Although polyploidization, a significant factor in plant evolution, leads to phenotypic changes, the roles of m<sup>6</sup>A in plant polyploidization remain unclear. Here, we observed increased leaf area, fresh weight, and thickness upon autotetraploidization in stevia (<i>Stevia rebaudiana</i>). To examine phenotypic and molecular changes following polyploidization, we quantified m<sup>6</sup>A abundance in RNA and conducted m<sup>6</sup>A immunoprecipitation sequencing (m<sup>6</sup>A-seq) and transcriptome analysis of autotetraploid and diploid stevia. Polyploidization led to increased m<sup>6</sup>A levels in RNA, especially in mRNA. m<sup>6</sup>A-seq methylome profiling revealed ~ 20,000 transcripts containing m<sup>6</sup>A, primarily in 3′ untranslated regions. Moreover, 2642 differentially modified m<sup>6</sup>A peaks (DMPs) were hypermethylated (hyper-DMPs) post polyploidization, and transcripts with hyper-DMPs were mainly associated with zeatin and flavonoid biosynthesis. Comparative analysis unveiled a possible correlation between m<sup>6</sup>A methylation and mRNA abundance, as confirmed by in vitro mRNA stability assays. The transcripts of many candidate genes involved in auxin, cytokinin, wax, and DNA biosynthesis, the cell cycle, and the cell wall exhibited hypermethylation and higher abundance in autotetraploid stevia. The contents of wax and auxin compounds significantly increased in autotetraploid stevia, suggesting that m<sup>6</sup>A modification helps maintain higher expression of these target genes. Our findings point to an m<sup>6</sup>A-orchestrated regulatory circuit where m<sup>6</sup>A hypermethylates and upregulates DMP-marked transcripts of auxin and wax biosynthesis genes, thereby determining the accumulation of auxin and wax compounds following stevia polyploidization, which contributes to the phenotypic changes following its autotetraploidization.</p>","PeriodicalId":20412,"journal":{"name":"Plant Growth Regulation","volume":"18 1","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dissecting the roles of increased mRNA m6A methylation in autotetraploidization in Stevia rebaudiana\",\"authors\":\"Juan Liu, Mingpu Tan, Yingying Zhang, Jie Zhao, Huijie Liu, Peng Liu, Wenna Meng, Anping Ding, Zengxu Xiang, Mingjia Chen\",\"doi\":\"10.1007/s10725-024-01199-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>N6-methyladenosine (m<sup>6</sup>A) is the most abundant modification in eukaryotic mRNA. m<sup>6</sup>A functions in embryo development, flowering time regulation, and fruit ripening. Although polyploidization, a significant factor in plant evolution, leads to phenotypic changes, the roles of m<sup>6</sup>A in plant polyploidization remain unclear. Here, we observed increased leaf area, fresh weight, and thickness upon autotetraploidization in stevia (<i>Stevia rebaudiana</i>). To examine phenotypic and molecular changes following polyploidization, we quantified m<sup>6</sup>A abundance in RNA and conducted m<sup>6</sup>A immunoprecipitation sequencing (m<sup>6</sup>A-seq) and transcriptome analysis of autotetraploid and diploid stevia. Polyploidization led to increased m<sup>6</sup>A levels in RNA, especially in mRNA. m<sup>6</sup>A-seq methylome profiling revealed ~ 20,000 transcripts containing m<sup>6</sup>A, primarily in 3′ untranslated regions. Moreover, 2642 differentially modified m<sup>6</sup>A peaks (DMPs) were hypermethylated (hyper-DMPs) post polyploidization, and transcripts with hyper-DMPs were mainly associated with zeatin and flavonoid biosynthesis. Comparative analysis unveiled a possible correlation between m<sup>6</sup>A methylation and mRNA abundance, as confirmed by in vitro mRNA stability assays. The transcripts of many candidate genes involved in auxin, cytokinin, wax, and DNA biosynthesis, the cell cycle, and the cell wall exhibited hypermethylation and higher abundance in autotetraploid stevia. The contents of wax and auxin compounds significantly increased in autotetraploid stevia, suggesting that m<sup>6</sup>A modification helps maintain higher expression of these target genes. Our findings point to an m<sup>6</sup>A-orchestrated regulatory circuit where m<sup>6</sup>A hypermethylates and upregulates DMP-marked transcripts of auxin and wax biosynthesis genes, thereby determining the accumulation of auxin and wax compounds following stevia polyploidization, which contributes to the phenotypic changes following its autotetraploidization.</p>\",\"PeriodicalId\":20412,\"journal\":{\"name\":\"Plant Growth Regulation\",\"volume\":\"18 1\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2024-08-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Growth Regulation\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s10725-024-01199-x\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PLANT SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Growth Regulation","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10725-024-01199-x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

N6-甲基腺苷(m6A)是真核生物 mRNA 中最丰富的修饰。m6A 在胚胎发育、花期调节和果实成熟中发挥作用。虽然多倍体化是植物进化的一个重要因素,会导致表型变化,但 m6A 在植物多倍体化中的作用仍不清楚。在这里,我们观察到甜叶菊(Stevia rebaudiana)自四倍体化后叶片面积、鲜重和厚度增加。为了研究多倍体化后的表型和分子变化,我们对 RNA 中的 m6A 丰度进行了量化,并对自四倍体和二倍体甜叶菊进行了 m6A 免疫沉淀测序(m6A-seq)和转录组分析。多倍体化导致 RNA 中 m6A 含量增加,尤其是在 mRNA 中。m6A-seq 甲基化组分析发现约 20,000 个转录本含有 m6A,主要在 3′非翻译区。此外,多倍体化后有2642个不同修饰的m6A峰(DMPs)被高甲基化(hyper-DMPs),具有高DMPs的转录本主要与玉米素和黄酮类化合物的生物合成有关。比较分析揭示了 m6A 甲基化与 mRNA 丰度之间可能存在的相关性,体外 mRNA 稳定性测定也证实了这一点。在自交系甜叶菊中,许多涉及辅酶、细胞分裂素、蜡质、DNA 生物合成、细胞周期和细胞壁的候选基因的转录本都表现出高甲基化和更高的丰度。在自交系甜叶菊中,蜡和辅助素化合物的含量显著增加,这表明 m6A 修饰有助于维持这些目标基因的高表达。我们的研究结果表明,在 m6A 协调的调控回路中,m6A 对辅素和蜡生物合成基因的 DMP 标记转录本进行超甲基化和上调,从而决定了甜叶菊多倍体化后辅素和蜡化合物的积累,这有助于甜叶菊自四倍体化后的表型变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dissecting the roles of increased mRNA m6A methylation in autotetraploidization in Stevia rebaudiana

Dissecting the roles of increased mRNA m6A methylation in autotetraploidization in Stevia rebaudiana

N6-methyladenosine (m6A) is the most abundant modification in eukaryotic mRNA. m6A functions in embryo development, flowering time regulation, and fruit ripening. Although polyploidization, a significant factor in plant evolution, leads to phenotypic changes, the roles of m6A in plant polyploidization remain unclear. Here, we observed increased leaf area, fresh weight, and thickness upon autotetraploidization in stevia (Stevia rebaudiana). To examine phenotypic and molecular changes following polyploidization, we quantified m6A abundance in RNA and conducted m6A immunoprecipitation sequencing (m6A-seq) and transcriptome analysis of autotetraploid and diploid stevia. Polyploidization led to increased m6A levels in RNA, especially in mRNA. m6A-seq methylome profiling revealed ~ 20,000 transcripts containing m6A, primarily in 3′ untranslated regions. Moreover, 2642 differentially modified m6A peaks (DMPs) were hypermethylated (hyper-DMPs) post polyploidization, and transcripts with hyper-DMPs were mainly associated with zeatin and flavonoid biosynthesis. Comparative analysis unveiled a possible correlation between m6A methylation and mRNA abundance, as confirmed by in vitro mRNA stability assays. The transcripts of many candidate genes involved in auxin, cytokinin, wax, and DNA biosynthesis, the cell cycle, and the cell wall exhibited hypermethylation and higher abundance in autotetraploid stevia. The contents of wax and auxin compounds significantly increased in autotetraploid stevia, suggesting that m6A modification helps maintain higher expression of these target genes. Our findings point to an m6A-orchestrated regulatory circuit where m6A hypermethylates and upregulates DMP-marked transcripts of auxin and wax biosynthesis genes, thereby determining the accumulation of auxin and wax compounds following stevia polyploidization, which contributes to the phenotypic changes following its autotetraploidization.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant Growth Regulation
Plant Growth Regulation 生物-植物科学
CiteScore
6.90
自引率
9.50%
发文量
139
审稿时长
4.5 months
期刊介绍: Plant Growth Regulation is an international journal publishing original articles on all aspects of plant growth and development. We welcome manuscripts reporting question-based research using hormonal, physiological, environmental, genetical, biophysical, developmental or molecular approaches to the study of plant growth regulation. Emphasis is placed on papers presenting the results of original research. Occasional reviews on important topics will also be welcome. All contributions must be in English.
×
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