{"title":"The PDR-type ABC transporter OsPDR1 is involved in leaf senescence by influencing melatonin biosynthesis in rice","authors":"Junming Zheng, Jinjin Ge, Pengyu Li, Boning Xin, Feng Lin, Wenhua Zhang, Wen Jing","doi":"10.1016/j.bbrc.2025.151355","DOIUrl":null,"url":null,"abstract":"<div><div>Leaf senescence is a complex developmental process that is regulated by multiple genetic and environmental factors. Understanding the mechanisms underlying the regulation of leaf senescence will provide valuable insights for manipulation of this trait in crops. Here, we report that the ATP-binding cassette (ABC) transporter OsPDR1 is involved in promoting leaf senescence in rice. Mutation and overexpression of <em>OsPDR1</em> delayed and accelerated natural leaf senescence at the seedling and mature stages, respectively. The level of <em>OsPDR1</em> transcript in leaves was significantly upregulated by dark treatment. Overexpression of <em>OsPDR1</em> accelerated dark-induced leaf senescence by enhancing senescence-associated gene expression, whereas its mutation delayed dark-induced leaf senescence. <em>OsPDR1</em> is coexpressed with the rice <em>N</em>-acetylserotonin methyltransferase gene, <em>OsASMT1</em>, encoding a key enzyme in melatonin biosynthesis. <em>OsASMT1</em> expression levels and melatonin content were significantly decreased in <em>OsPDR1</em>-overexpressing lines but significantly increased in <em>ospdr1</em> mutants compared to the wild type. Exogenous melatonin application markedly decreased the accumulation of reactive oxygen species (ROS) and delayed leaf senescence in <em>PDR1.3</em>-overexpressing plants. These results indicated that OsPDR1 plays an important role in the regulation of leaf senescence by influencing melatonin biosynthesis in rice.</div></div>","PeriodicalId":8779,"journal":{"name":"Biochemical and biophysical research communications","volume":"749 ","pages":"Article 151355"},"PeriodicalIF":2.5000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochemical and biophysical research communications","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0006291X25000695","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Leaf senescence is a complex developmental process that is regulated by multiple genetic and environmental factors. Understanding the mechanisms underlying the regulation of leaf senescence will provide valuable insights for manipulation of this trait in crops. Here, we report that the ATP-binding cassette (ABC) transporter OsPDR1 is involved in promoting leaf senescence in rice. Mutation and overexpression of OsPDR1 delayed and accelerated natural leaf senescence at the seedling and mature stages, respectively. The level of OsPDR1 transcript in leaves was significantly upregulated by dark treatment. Overexpression of OsPDR1 accelerated dark-induced leaf senescence by enhancing senescence-associated gene expression, whereas its mutation delayed dark-induced leaf senescence. OsPDR1 is coexpressed with the rice N-acetylserotonin methyltransferase gene, OsASMT1, encoding a key enzyme in melatonin biosynthesis. OsASMT1 expression levels and melatonin content were significantly decreased in OsPDR1-overexpressing lines but significantly increased in ospdr1 mutants compared to the wild type. Exogenous melatonin application markedly decreased the accumulation of reactive oxygen species (ROS) and delayed leaf senescence in PDR1.3-overexpressing plants. These results indicated that OsPDR1 plays an important role in the regulation of leaf senescence by influencing melatonin biosynthesis in rice.
期刊介绍:
Biochemical and Biophysical Research Communications is the premier international journal devoted to the very rapid dissemination of timely and significant experimental results in diverse fields of biological research. The development of the "Breakthroughs and Views" section brings the minireview format to the journal, and issues often contain collections of special interest manuscripts. BBRC is published weekly (52 issues/year).Research Areas now include: Biochemistry; biophysics; cell biology; developmental biology; immunology
; molecular biology; neurobiology; plant biology and proteomics