Effects of functional defects in the NMD pathway on rice phenotype and transcriptome.

Q3 Medicine 遗传 Pub Date : 2024-07-01 DOI:10.16288/j.yczz.24-063
Yue-Yang Wu, Xiao-Yan Zhou, Yu-Feng Wu, Ju Huang
{"title":"Effects of functional defects in the NMD pathway on rice phenotype and transcriptome.","authors":"Yue-Yang Wu, Xiao-Yan Zhou, Yu-Feng Wu, Ju Huang","doi":"10.16288/j.yczz.24-063","DOIUrl":null,"url":null,"abstract":"<p><p>Nonsense-mediated mRNA decay (NMD) is an important RNA quality control pathway. It aids in degrading harmful erroneous mRNA, thereby preserving a stable and healthy internal environment. In this study, we employed CRISPR/Cas9 and amiRNA technology to generate knock out or knock down mutants of realted genes in the rice NMD pathway. Through transcriptome sequencing and observing phenotype changes, the study explored the impact of NMD pathway defects on rice gene expression and alternative splicing. The results suggest that even partial defects will induce phenotypic changes such as plant height and pollen vitality to different degrees, showing necessity of NMD factors. Gene expression analysis reveals that most differentially expressed genes are upregulated in the mutants, with <i>ko-upf1-like</i> and <i>kd-upf1</i> defects having a more significant impact than <i>kd-upf2</i> and <i>kd-upf3</i>. Specifically, NMD pathway defects result in increased expression levels of rice defense response-related genes and decreased expression levels of secondary metabolism-related genes, with a wider range of affected genes observed in 60-day-old senescence mutants. Transcript analysis indicates that different NMD related genes defects alter hundreds of alternative splicing events, mostly enriched in genes involving alternative splicing regulatory pathways. Approximately half of these events are shared among different mutants, and a substantial number of affected transcripts show NMD target features. NMD could affect both the transcript abundance and their splicing subtypes to regulate the defense response and early-senescence associated pathways, which plays a vital role in rice growth and reproduction.</p>","PeriodicalId":35536,"journal":{"name":"遗传","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"遗传","FirstCategoryId":"1091","ListUrlMain":"https://doi.org/10.16288/j.yczz.24-063","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Nonsense-mediated mRNA decay (NMD) is an important RNA quality control pathway. It aids in degrading harmful erroneous mRNA, thereby preserving a stable and healthy internal environment. In this study, we employed CRISPR/Cas9 and amiRNA technology to generate knock out or knock down mutants of realted genes in the rice NMD pathway. Through transcriptome sequencing and observing phenotype changes, the study explored the impact of NMD pathway defects on rice gene expression and alternative splicing. The results suggest that even partial defects will induce phenotypic changes such as plant height and pollen vitality to different degrees, showing necessity of NMD factors. Gene expression analysis reveals that most differentially expressed genes are upregulated in the mutants, with ko-upf1-like and kd-upf1 defects having a more significant impact than kd-upf2 and kd-upf3. Specifically, NMD pathway defects result in increased expression levels of rice defense response-related genes and decreased expression levels of secondary metabolism-related genes, with a wider range of affected genes observed in 60-day-old senescence mutants. Transcript analysis indicates that different NMD related genes defects alter hundreds of alternative splicing events, mostly enriched in genes involving alternative splicing regulatory pathways. Approximately half of these events are shared among different mutants, and a substantial number of affected transcripts show NMD target features. NMD could affect both the transcript abundance and their splicing subtypes to regulate the defense response and early-senescence associated pathways, which plays a vital role in rice growth and reproduction.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
NMD 通路功能缺陷对水稻表型和转录组的影响
无义介导的 mRNA 衰变(NMD)是一种重要的 RNA 质量控制途径。它有助于降解有害的错误 mRNA,从而保持稳定健康的内环境。在这项研究中,我们利用 CRISPR/Cas9 和 amiRNA 技术生成了水稻 NMD 通路中相关基因的基因敲除或基因敲低突变体。通过转录组测序和观察表型变化,该研究探讨了 NMD 通路缺陷对水稻基因表达和替代剪接的影响。结果表明,即使是部分缺陷,也会在不同程度上引起植株高度和花粉活力等表型变化,显示了 NMD 因子的必要性。基因表达分析表明,大多数差异表达基因在突变体中上调,其中 ko-upf1-like 和 kd-upf1 缺陷的影响比 kd-upf2 和 kd-upf3 更为显著。具体来说,NMD 途径缺陷导致水稻防御反应相关基因的表达水平升高,次生代谢相关基因的表达水平降低,在 60 天衰老突变体中观察到的受影响基因范围更广。转录本分析表明,不同的 NMD 相关基因缺陷改变了数百个替代剪接事件,其中大部分富集在涉及替代剪接调控途径的基因中。这些事件中约有一半是不同突变体共有的,大量受影响的转录本显示出 NMD 的目标特征。NMD 可影响转录本的丰度及其剪接亚型,从而调控防御反应和早期衰老相关途径,这对水稻的生长和繁殖起着至关重要的作用。
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 去求助
来源期刊
遗传
遗传 Medicine-Medicine (all)
CiteScore
2.50
自引率
0.00%
发文量
6699
期刊介绍:
期刊最新文献
Advancements and prospects in reconstructing the genetic genealogies of ancient and modern human populations using ancestral recombination graphs. Advances in high throughput sequencing methods for DNA damage and repair. Application of Mendelian randomization analysis in investigating the genetic background of blood biomarkers for colorectal cancer. Computational dissection of the regulatory mechanisms of aberrant metabolism in remodeling the microenvironment of breast cancer. Gut metagenome-derived image augmentation and deep learning improve prediction accuracy of metabolic disease classification.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1