PEN1 catalyses RNA primer removal during plastid DNA replication in maize

IF 15.8 1区 生物学 Q1 PLANT SCIENCES
Xing Huang, Guolong Shi, Qiao Xiao, Jiaojiao Feng, Yongcai Huang, Hai Shi, Qiong Wang, Yu Su, Jiechen Wang, Xingguo Wu, Yuwei Cao, Haihai Wang, Wenqin Wang, Yu Zhang, Yongrui Wu
{"title":"PEN1 catalyses RNA primer removal during plastid DNA replication in maize","authors":"Xing Huang, Guolong Shi, Qiao Xiao, Jiaojiao Feng, Yongcai Huang, Hai Shi, Qiong Wang, Yu Su, Jiechen Wang, Xingguo Wu, Yuwei Cao, Haihai Wang, Wenqin Wang, Yu Zhang, Yongrui Wu","doi":"10.1038/s41477-025-02027-4","DOIUrl":null,"url":null,"abstract":"<p>The plastid DNA (ptDNA) replication is initiated by primases, which synthesize RNA primers; following the synthesis of DNA fragments, primers must be removed before ligation. However, the enzymes and mechanisms underlying this process are poorly understood. Here we cloned a gene from maize that encodes a plastid-localized and Mn<sup>2+</sup>-dependent 5′–3′ exonuclease (designated PEN1) responsible for this process. The <i>pen1</i> seeds show development and filling defects that intensify across generations. PEN1 cleaves the RNA primers, allowing for the complete excision of ribonucleotides. We reconstituted the plastid RNA primer removal processes in vitro. We also determined the crystal structure of the PEN1–dsDNA binary complex and explained the structural mechanism of the 5′ to 3′ exonuclease activity. Mutation of <i>Pen1</i> resulted in the accumulation of ptDNA breaks, thereby compromising plastid function. These studies fill a critical gap that has long existed in the understanding of ptDNA replication.</p>","PeriodicalId":18904,"journal":{"name":"Nature Plants","volume":"39 1","pages":""},"PeriodicalIF":15.8000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Plants","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1038/s41477-025-02027-4","RegionNum":1,"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

Abstract

The plastid DNA (ptDNA) replication is initiated by primases, which synthesize RNA primers; following the synthesis of DNA fragments, primers must be removed before ligation. However, the enzymes and mechanisms underlying this process are poorly understood. Here we cloned a gene from maize that encodes a plastid-localized and Mn2+-dependent 5′–3′ exonuclease (designated PEN1) responsible for this process. The pen1 seeds show development and filling defects that intensify across generations. PEN1 cleaves the RNA primers, allowing for the complete excision of ribonucleotides. We reconstituted the plastid RNA primer removal processes in vitro. We also determined the crystal structure of the PEN1–dsDNA binary complex and explained the structural mechanism of the 5′ to 3′ exonuclease activity. Mutation of Pen1 resulted in the accumulation of ptDNA breaks, thereby compromising plastid function. These studies fill a critical gap that has long existed in the understanding of ptDNA replication.

Abstract Image

玉米质体DNA复制过程中,PEN1催化RNA引物去除
质体DNA (ptDNA)的复制由引物启动,引物合成RNA引物;在DNA片段合成之后,在结扎之前必须移除引物。然而,人们对这一过程背后的酶和机制知之甚少。在这里,我们从玉米中克隆了一个基因,该基因编码负责这一过程的质体定位和Mn2+依赖的5 ‘ -3 ’外切酶(称为PEN1)。pen1种子表现出发育和填充缺陷,这种缺陷在几代之间加剧。PEN1切割RNA引物,允许核糖核苷酸的完全切除。我们在体外重建了质体RNA引物的去除过程。我们还确定了PEN1-dsDNA二元复合物的晶体结构,并解释了5 ‘至3 ’外切酶活性的结构机制。Pen1突变导致ptDNA断裂积累,从而损害质体功能。这些研究填补了长期以来在理解ptDNA复制方面存在的一个关键空白。
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
Nature Plants
Nature Plants PLANT SCIENCES-
CiteScore
25.30
自引率
2.20%
发文量
196
期刊介绍: Nature Plants is an online-only, monthly journal publishing the best research on plants — from their evolution, development, metabolism and environmental interactions to their societal significance.
×
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