Evidence map›Paper›PMID 34351541›Full record

ArticleMolecular biology reports2021

CRISPR/Cas9-mediated mutagenesis of WRKY3 and WRKY4 function decreases salt and Me-JA stress tolerance in Arabidopsis thaliana.

Peng Li, Xiwen Li, Min Jiang

Abstract read
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Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.2field-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

29 citing papers in PubMed, 69 citations in OpenAlex.

  1. Advances in CRISPR Plant Applications.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Genome-wide analysis of DC1 domain proteins inFrontiers in plant science · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. The role of DNA content in shaping chromatin architecture and gene expression.The Plant journal : for cell and molecular biology · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Comprehensive Expression Analysis of the WRKY Gene Family inInternational journal of molecular sciences · 2024
    Article
  16. Review
  17. Article
  18. Review
  19. Gene Expression and Interaction Analysis ofPlants (Basel, Switzerland) · 2023
    Article
  20. Article
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

3 authors at 2 institutions in 1 country.

Peng Li *Shanghai Key Laboratory of Plant Functional Genomics and Resources, Shanghai Chenshan Botanical Garden, Shanghai, 201602, China.
Xiwen Li *Shanghai Key Laboratory of Plant Functional Genomics and Resources, Shanghai Chenshan Botanical Garden, Shanghai, 201602, China.
Min JiangMinistry of Education Key Laboratory for Biodiversity Science and Ecological Engineering, Institute of Biodiversity Science, School of Life Sciences, Fudan University, Shanghai, 200438, China. 20110700001@fudan.edu.cn.ORCID http://orcid.org/0000-0002-0757-9217
Shanghai Chenshan Plant Science Research Center · CNFudan University · CN

Funding

Shanghai Sailing Program 19YF1414800
6 · The paper itself

Abstract

backgroundWRKY transcription factor is involved in regulation of plant growth and development, response to biotic and abiotic stresses, including homologous WRKY3 and WRKY4 genes which play a vital role in regulating plants defense response to pathogen and drought stress. METHODS AND

resultsTo investigate the function of AtWRKY3 and AtWRKY4 genes in regulating salt and Me-JA stresses, the loss-of-function mutations were generated by clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated 9 (Cas9) system in Arabidopsis thaliana. Several independent transgenic lines with single or double mutations were obtained via Agrobacterium-mediated transformation. The knockout lines of AtWRKY3 and AtWRKY4 genes were successfully achieved and confirmed by qRT-PCR technology. Expression analysis showed that AtWRKY3 and AtWRKY4 genes had significantly up-regulated under salt and Me-JA stresses. The growth of double mutant plants under salt or Me-JA stresses were significantly inhibited compared with corresponding wild type (WT) plants, especially their root lengths. Moreover, the double mutant plants displayed salt and Me-JA sensitivity phenotypic characteristics, such as the increased relative electrolyte leakage (REL) and a substantial reduce in the activities of antioxidant enzymes, including superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT) activities.

conclusionTaken together, these data suggested that the simultaneous modification of homologous gene copies of WRKY are established using CRISPR/Cas9 system in A. thaliana and the loss of AtWRKY3 and AtWRKY4 has an effect on ROS scavenging pathways to reduce stress tolerance.

Indexed as

ArabidopsisArabidopsis ProteinsCRISPR-Cas SystemsDroughtsGene ExpressionGene Expression Regulation, PlantGenetic EngineeringPlant ProteinsPlants, Genetically ModifiedPolymorphism, Single NucleotideSalt StressSalt ToleranceSodium ChlorideStress, PhysiologicalTranscription FactorsArabidopsis ProteinsPlant ProteinsSodium ChlorideTranscription FactorsWRKY3 protein, ArabidopsisWRKY4 protein, ArabidopsisArabidopsis thalianaCRISPR/Cas9 systemMe-JA stressSalt stressWRKY transcription factors

Identifiers

PMID34351541
OpenAlexW3190618323

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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.