Evidence map›Paper›PMID 40107853›Full record

ArticleThe plant genome2025

A 24-nt miR9560 modulates the transporter gene BrpHMA2 expression in Brassica parachinensis.

Yongsheng Bai, Xiaoting Wang, Shahid Ali, Yang Liu, Jiannan Zhou, Meiting Liu, Shuai Liu, Yulin Tang

Abstract read
In one paragraph

Article in The plant genome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Exploring the CeRNA landscape in plants: advances, methods, and challenges.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2026
    Review
  2. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Yongsheng BaiGuangdong Provincial Key Laboratory for Plant Epigenetics, Guangdong Technology Research Center for Marine Algal Bioengineering, Shenzhen Public Service Platform of Collaborative Innovation for Marine Algae Industry, Longhua Institute of Innovative Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Xiaoting WangShaanxi Academy of Traditional Chinese Medicine, Xi'an, China.
Shahid AliGuangdong Provincial Key Laboratory for Plant Epigenetics, Guangdong Technology Research Center for Marine Algal Bioengineering, Shenzhen Public Service Platform of Collaborative Innovation for Marine Algae Industry, Longhua Institute of Innovative Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Yang LiuShaanxi Academy of Traditional Chinese Medicine, Xi'an, China.
Jiannan ZhouKey Laboratory of Tropical Fruit Biology (Ministry of Agriculture), South Subtropical Crops Research Institute, Chinese Academy of Tropical Agricultural Sciences, Zhanjiang, China.
Meiting LiuGuangdong Provincial Key Laboratory for Plant Epigenetics, Guangdong Technology Research Center for Marine Algal Bioengineering, Shenzhen Public Service Platform of Collaborative Innovation for Marine Algae Industry, Longhua Institute of Innovative Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Shuai LiuGuangdong Provincial Key Laboratory for Plant Epigenetics, Guangdong Technology Research Center for Marine Algal Bioengineering, Shenzhen Public Service Platform of Collaborative Innovation for Marine Algae Industry, Longhua Institute of Innovative Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.
Yulin TangGuangdong Provincial Key Laboratory for Plant Epigenetics, Guangdong Technology Research Center for Marine Algal Bioengineering, Shenzhen Public Service Platform of Collaborative Innovation for Marine Algae Industry, Longhua Institute of Innovative Biotechnology, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen, China.ORCID https://orcid.org/0000-0002-7098-8558

Funding

Guangdong Innovation Research Team Fund 2014ZT05S078Shenzhen Natural Science Fund 20220804115333001
6 · The paper itself

Abstract

MicroRNAs (miRNAs) control gene expression in plant through transcript cleavage and translation inhibition. Recently, 24-nt miRNAs have been shown to direct DNA methylation at target sites, regulating the neighboring gene expression. Our study focused on miR9560, a 24-nt miRNA induced by cadmium (Cd) stress in Brassica rapa ssp. parachinensis (B. parachinensis). Phylogenetic analysis revealed miR9560 predominantly emerged in the Rosanae superorder and was conserved in Brassicaceae, with potential target sites adjacent to transporter family genes HMAs. RNA gel blotting showed that mature miR9560 was only detected in various Brassica crops roots after Cd stress. In B. parachinensis, miR9560's putative target site is upstream of BrpHMA2, an afflux-type Cd transporter. In a transient expression system of B. parachinensis protoplasts, the expression of miR9560 increased the DNA methylation upstream of BrpHMA2, reducing the transcription of BrpHMA2. This regulation was also observed in Arabidopsis wild-type protoplasts but not in the mutants dcl234 and ago4 with impairments in the RNA-dependent DNA methylation (RdDM) pathway. We deduced that miR9560 modulates BrpHMA2 expression via the RdDM pathway, potentially regulating Cd uptake and movement in B. parachinensis. Furthermore, this regulatory mechanism may extend to other Brassica plants. This study enhances our comprehension of 24-nt miRNAs role in regulating Cd accumulation within Brassica plants.

Indexed as

BrassicaGene Expression Regulation, PlantMicroRNAsPlant ProteinsArabidopsisCadmiumDNA MethylationPhylogenyRNA, PlantCadmiumMicroRNAsPlant ProteinsRNA, Plant

Identifiers

PMID40107853
PMCPMC11922684

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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 OpenQuestion graph.