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The long non-coding RNA PILNCR2 increases low phosphate tolerance in maize by interfering with miRNA399-guided cleavage of ZmPHT1s

作     者:Yafei Wang Zhonghua Wang Qingguo Du Kai Wang Chunqin Zou Wen-Xue Li Yafei Wang;Zhonghua Wang;Qingguo Du;Kai Wang;Chunqin Zou;Wen-Xue Li

作者机构:National Engineering Laboratory for Crop Molecular BreedingInstitute of Crop SciencesChinese Academy of Agricultural SciencesBeijing 100081China College of Resources and Environmental SciencesNational Academy of Agriculture Green DevelopmentKey Laboratory of Plant-Soil InteractionsMinistry of EducationChina Agricultural UniversityBeijing100193China 

出 版 物:《Molecular Plant》 (分子植物(英文版))

年 卷 期:2023年第16卷第7期

页      面:1146-1159页

核心收录:

学科分类:0710[理学-生物学] 09[农学] 0901[农学-作物学] 

基  金:the National Key Research and Development Program of China(2021YFF1000500) the Agricultural Science and Technology Innovation Program of CAAS to W.-X.L. 

主  题:long non-coding RNA miRNA RNA/RNA duplex post-transcriptional regulation maize 

摘      要:Theopen reading regions of ZmPHT1s(inorganic phosphate[Pij transporters)inmaize possess target sites of microRNA399(miR399).However,the relationship between miR399 and ZmPHT1s and its functional importance in response to Pi deficiency remain to be explored.We show here that ZmPHT1;1,ZmPHT1;3,and ZmPHT1;13 are the targets of ZmmiRNA399.We found that a long non-coding RNA,PILNCR2(Pi-deficiency-induced IncRNA 2),is transcribed from the opposing DNA strand of ZmPHT1;1 and predominantly localized in the cytoplasm.A ribonuclease protection assay and an RNA-RNA binding assay showed that PILNCR2 and ZmPHT1s could form the RNA/RNA duplexes in vivo and in vitro.A co-expression assay in N.benthamiana revealed that the PILNCR2/ZmPHT1 RNA/RNA duplexes interfere with miR399-guided cleavage of ZmPHT1 mRNAs.Overexpression of PILNCR2 increased low-Pi tolerance in maize,whereas its knockout and knockdown decreased low-Pi tolerance in maize.Consistently,ZmPHT1;3 and ZmPHT1;13 mRNA abundance was increased in transgenic plants overexpressing PILNCR2 but reduced in its knock-out mutants,suggesting that PILNCR2 positively regulates the mRNA abundance of ZmPHT1;3 and ZmPHT1;13 in maize.Collectively,these results indicate that PILNCR2 plays an important role in maize Pihomeostasisby interfering with miRNA399-guided cleavageof ZmPHT1mRNAs.

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