Selective recruitment of NAT10-catalyzed ac4C-modified mRNAs into stress granules by poly(A)-binding protein promotes mRNA stability and plant heat-stress tolerance.

IF 32.7 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Plant Pub Date : 2026-10-05 Epub Date: 2026-08-10 DOI:10.1016/j.molp.2026.08.004
Wanhong Zhang, Yanxiao Bu, Yubing Jiao, Yingwen Wang, Lili Shen, Ying Li, Binna Lv, Tzu-Chieh Ho, Yih-Cherng Liou, Chin-Kuo Chen, Fei Han, Robert Y L Wang, Jinguang Yang
{"title":"Selective recruitment of NAT10-catalyzed ac<sup>4</sup>C-modified mRNAs into stress granules by poly(A)-binding protein promotes mRNA stability and plant heat-stress tolerance.","authors":"Wanhong Zhang, Yanxiao Bu, Yubing Jiao, Yingwen Wang, Lili Shen, Ying Li, Binna Lv, Tzu-Chieh Ho, Yih-Cherng Liou, Chin-Kuo Chen, Fei Han, Robert Y L Wang, Jinguang Yang","doi":"10.1016/j.molp.2026.08.004","DOIUrl":null,"url":null,"abstract":"<p><p>Global warming poses a considerable threat to crop production, making heat stress a challenge in agriculture, yet how epitranscriptomic modifications contribute to plant heat-stress responses remains to be explored. This study reveals the role of phase separation in plant heat-stress tolerance and shows that N-acetyltransferase 10 (NAT10), which encodes a cytosine N4 acetyltransferase, contributes to heat resistance. We found that NAT10 interacts with polyadenylate-binding protein (PABP), which contains intrinsically disordered regions, thereby facilitating the selective recruitment of ac<sup>4</sup>C-modified mRNAs into PABP-mediated condensates. Integrative transcriptome-wide analysis, combining ac<sup>4</sup>C acetylome profiling with stress-granule-enriched transcript sequencing, revealed that detoxification-related mRNAs, including those encoding the cytochrome P450, phenylalanine ammonia-lyase, glutathione S-transferase, and heat shock 70 protein families, preferentially accumulate within these condensates. This accumulation maintains their stability and prevents stress-induced degradation. Conversely, loss of PABP function impairs the recruitment of ac<sup>4</sup>C-modified detoxification-related transcripts into stress granules, thereby promoting their degradation under heat stress. In summary, our findings identify a stress-responsive NAT10-PABP-ac<sup>4</sup>C axis that promotes phase separation to stabilize ac<sup>4</sup>C-modified mRNAs under heat stress. By recruiting detoxification-related transcripts into stress granules, this axis ensures mRNA stability under environmental stress, offering new insights for enhancing crop stress resilience.</p>","PeriodicalId":19012,"journal":{"name":"Molecular Plant","volume":" ","pages":"2122-2139"},"PeriodicalIF":32.7000,"publicationDate":"2026-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Plant","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.molp.2026.08.004","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/10 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Global warming poses a considerable threat to crop production, making heat stress a challenge in agriculture, yet how epitranscriptomic modifications contribute to plant heat-stress responses remains to be explored. This study reveals the role of phase separation in plant heat-stress tolerance and shows that N-acetyltransferase 10 (NAT10), which encodes a cytosine N4 acetyltransferase, contributes to heat resistance. We found that NAT10 interacts with polyadenylate-binding protein (PABP), which contains intrinsically disordered regions, thereby facilitating the selective recruitment of ac4C-modified mRNAs into PABP-mediated condensates. Integrative transcriptome-wide analysis, combining ac4C acetylome profiling with stress-granule-enriched transcript sequencing, revealed that detoxification-related mRNAs, including those encoding the cytochrome P450, phenylalanine ammonia-lyase, glutathione S-transferase, and heat shock 70 protein families, preferentially accumulate within these condensates. This accumulation maintains their stability and prevents stress-induced degradation. Conversely, loss of PABP function impairs the recruitment of ac4C-modified detoxification-related transcripts into stress granules, thereby promoting their degradation under heat stress. In summary, our findings identify a stress-responsive NAT10-PABP-ac4C axis that promotes phase separation to stabilize ac4C-modified mRNAs under heat stress. By recruiting detoxification-related transcripts into stress granules, this axis ensures mRNA stability under environmental stress, offering new insights for enhancing crop stress resilience.

通过聚(A)结合蛋白选择性募集nat10催化的ac4c修饰mRNA进入胁迫颗粒,促进mRNA稳定性和植物耐热性。
全球变暖对农作物生产构成了相当大的威胁,使热应激成为农业的关键挑战。然而,表观转录组修饰如何促进植物热胁迫反应仍有待探索。本研究揭示了相分离在植物耐热性中的关键作用,并证明了编码胞嘧啶N4乙酰转移酶蛋白的n -乙酰转移酶10 (NAT10)在耐热性中起着重要作用。我们发现NAT10与含有内在无序区(IDRs)的聚腺苷酸结合蛋白(PABP)相互作用,从而促进ac4c修饰的mrna选择性募集到PABP介导的凝聚物中。综合转录组分析,结合ac4C乙酰基谱分析和gs富集转录物测序,揭示了解毒相关mrna,包括编码细胞色素P450、苯丙氨酸解氨酶、谷胱甘肽s转移酶和热休克70蛋白家族的mrna,优先在这些凝聚物中积累。这种积累保持了它们的稳定性,并防止应力引起的降解。相反,PABP的缺失会损害ac4c修饰的解毒相关转录本在胁迫颗粒中的募集,从而促进它们在热胁迫下的降解。总之,我们的研究结果确定了一个应激响应的NAT10-PABP-ac4C轴,该轴促进相分离以稳定热应激下ac4c修饰的mrna。通过将解毒相关转录本招募到胁迫颗粒中,该轴确保了mRNA的稳定性,并为提高作物在环境胁迫下的抗逆性提供了见解。
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
Molecular Plant
Molecular Plant 植物科学-生化与分子生物学
CiteScore
37.60
自引率
2.20%
发文量
1784
审稿时长
1 months
期刊介绍: Molecular Plant is dedicated to serving the plant science community by publishing novel and exciting findings with high significance in plant biology. The journal focuses broadly on cellular biology, physiology, biochemistry, molecular biology, genetics, development, plant-microbe interaction, genomics, bioinformatics, and molecular evolution. Molecular Plant publishes original research articles, reviews, Correspondence, and Spotlights on the most important developments in plant biology.
×
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:604180095
Book学术官方微信
小红书