Evidence map›Paper›PMID 36460977›Full record

ArticleBMC plant biology2022

Suppression of microRNA168 enhances salt tolerance in rice (Oryza sativa L.).

Jiong Wan, Shujun Meng, Qiyue Wang, Jiawen Zhao, Xiaoqian Qiu, Liangfa Wang, Juan Li, Yuan Lin, Liqin Mu, Kuntai Dang and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.8field-weighted citation impact, top 7% of its field
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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Insights into the Epigenetic Basis of Plant Salt Tolerance.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
  10. Review
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

14 authors at 4 institutions in 2 countries.

Jiong Wan *National Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Shujun Meng *National Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Qiyue WangNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Jiawen ZhaoNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Xiaoqian QiuNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Liangfa WangHebi Academy of Agricultural Sciences, 458030, Hebi, China.
Juan LiInstitute of Crop Germplasm Resources, Guizhou Academy of Agricultural Sciences, 550006, Guiyang, China.
Yuan LinHebi Academy of Agricultural Sciences, 458030, Hebi, China.
Liqin MuNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Kuntai DangNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Qiankun XieNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Jihua TangNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China.
Dong DingNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China. dingdong0216@hotmail.com.
Zhanhui ZhangNational Key Laboratory of Wheat and Maize Crop Science, College of Agronomy, Henan Agricultural University, 450002, Zhengzhou, China. zhanhui17@henau.edu.cn.
Henan Agricultural University · CNHaute École de Bruxelles · BEChina Shenhua Energy (China) · CNGuizhou Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRice is a salt-sensitive crop. Complex gene regulatory cascades are likely involved in salinity stress in rice roots. microRNA168 (miR168) is a conserved miRNA among different plant species. It in-directly regulates the expression of all miRNAs by targeting gene ARGONAUTE1(AGO1). Short Tandem Target Mimic (STTM) technology is an ideal approach to study miRNA functions by in-activating mature miRNA in plants.

resultsIn this study, rice miR168 was inactivated by STTM. The T3 generation seedlings of STTM168 exhibited significantly enhanced salt resistance. Direct target genes of rice miR168 were obtained by in silico prediction and further confirmed by degradome-sequencing. PINHEAD (OsAGO1), which was previously suggested to be a plant abiotic stress response regulator. RNA-Seq was performed in root samples of 150mM salt-treated STTM168 and control seedlings. Among these screened 481 differentially expressed genes within STTM168 and the control, 44 abiotic stress response related genes showed significant difference, including four known salt-responsive genes.

conclusionBased on sequencing and qRT-PCR, a "miR168-AGO1-downstream" gene regulation model was proposed to be responsible for rice salt stress response. The present study proved miR168-AGO1 cascade to play important role in rice salinity stress responding, as well as to be applied in agronomic improvement in further.

Indexed as

MicroRNAsOryzaSalt StressSalt ToleranceSeedlingsMicroRNAsGene regulation cascadesmiR168RiceSalt stressSTTM

Identifiers

PMID36460977
PMCPMC9719116
OpenAlexW4310779927

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.