Evidence map›Paper›PMID 40437320›Full record

ArticlePlant cell reports2025

A novel-miR-164 from Atractylodes lancea targets AlNAC1 regulating leaf senescence.

Juan Deng, Xiao Huang, Meng Wang, Qian Li, Ling Gong, Bisheng Huang, Kun Yu

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Article in Plant cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Juan Deng *School of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China.
Xiao Huang *School of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China.
Meng WangSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China.
Qian LiSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China.
Ling GongSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China.
Bisheng HuangSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China.
Kun YuSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, 430065, China. kunyu@hbucm.edu.cn.ORCID http://orcid.org/0000-0002-4262-4431

Funding

National Natural Science Foundation of China 31670341
6 · The paper itself

Abstract

key messageA novel miR164-AlNAC1 module adjusting the expression of genes related to chlorophyll synthesis and ROS synthesis, and regulating leaf senescence in Atractylodes lancea. Leaf senescence is a critical developmental process regulated by complex genetic networks. In this study, a novel miRNA belonging to the MIR164 family was identified as a key regulator of leaf senescence in A. lancea by targeting the transcription factor AlNAC1. Bioinformatics analysis revealed that target gene AlNAC1 was closely related to the senescence-associated gene ANAC092 in Arabidopsis. The qRT-PCR and tobacco transient expression demonstrated nov-miR164 negatively regulated AlNAC1. Subcellular localization and transcriptional activity assays revealed that AlNAC1 localized to the nucleus and functioned as a transcriptional activator. Furthermore, EMSA experiments showed that AlNAC1 bound to the G-box motifs on the promoters of AlNYC, AlPAO, and AlRbohC. With the aging of A. lancea leaves, the expression of nov-miR164 decreased, while AlNAC1 and senescence-associated genes (AlSAG21, AlNYC, AlPAO, and AlRbohC) were significantly upregulated. Agrobacterium-mediated transient expression experiment results demonstrated that nov-miR164 negatively regulated AlNAC1 to suppress chlorophyll degradation and ROS accumulation, thereby delaying leaf senescence. Our findings provide new insights into the molecular mechanisms of leaf senescence in A. lancea and highlight the potential of nov-miR164 as a target for increasing crop yield and improving crop longevity.

Indexed as

AtractylodesMicroRNAsPlant LeavesPlant ProteinsPlant SenescenceTranscription FactorsChlorophyllGene Expression Regulation, PlantNicotianaPlants, Genetically ModifiedPromoter Regions, GeneticReactive Oxygen SpeciesChlorophyllMicroRNAsPlant ProteinsReactive Oxygen SpeciesTranscription FactorsAtractylodes lanceaChlorophyll degradationLeaf senescenceNACNovel miRNA

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.