Evidence map›Paper›PMID 41249860›Full record

ArticlePlant biotechnology journal2026

WRKY27-RAP2.7 Regulatory Module Promotes Cold Tolerance via Modulation of Lignin Biosynthesis and Redox Homeostasis by Regulating Cinnamyl Alcohol Dehydrogenase 7 and Glutathione S-Transferase F6.

Jing Qu, Peng Xiao, Yilei Wang, Tian Fang, Haowei Chen, Chunlong Li, Ji-Hong Liu

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Functional Characterization and Potential Regulatory Role ofInternational journal of molecular sciences · 2026
    Article
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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

7 authors.

Jing QuNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.
Peng XiaoNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.
Yilei WangNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.
Tian FangNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.
Haowei ChenNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.
Chunlong LiNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0002-4693-2925
Ji-Hong LiuNational Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.ORCID https://orcid.org/0000-0001-6686-1629

Funding

National Key Research and Development Program of China 2022YFD1200503National Natural Science Foundation of China 32330095
6 · The paper itself

Abstract

Cold stress adversely affects plant growth and development, significantly limiting fruit yield and quality in citrus. Ichang papeda (Citrus ichangensis), a cold-tolerant citrus species, serves as a valuable genetic resource for studying cold adaptation, yet the key genes and their modes of action underlying the cold stress response remain largely unexplored. In this study, we identified CiWRKY27 as a critical positive regulator of cold tolerance in Ichang papeda. Through DNA affinity purification sequencing (DAP-seq) and RNA-sequencing analyses we uncovered 717 potential target genes of CiWRKY27, many of which are associated with stress adaptation. Further investigation revealed that CiWRKY27 directly activated CiCAD7 and CiGSTF6 by binding to W-box elements in their promoters, thereby enhancing lignin biosynthesis and reactive oxygen species (ROS) detoxification to confer cold tolerance. Functional assays confirmed that both CiCAD7 and CiGSTF6 contributed positively to cold tolerance. Additionally, CiRAP2.7, an RAP2 (AP2/ERF) transcription factor, physically interacted with CiWRKY27 to synergistically amplify the activation of CiCAD7. Intriguingly, CiRAP2.7 was itself regulated by CiWRKY27 and functioned as a transcriptional activator of CiCAD7 for rendering cold tolerance. Taken together, our findings demonstrate that CiWRKY27 works, alone or together with CiRAP2.7, to modulate cold tolerance by regulating CiCAD7-mediated lignin biosynthesis and CiGSTF6-dependent ROS scavenging. This study gains valuable insights into the molecular regulation of lignin biosynthesis and ROS homeostasis under cold stress, and offers a promising molecular module for improving cold tolerance in citrus and other crops.

Indexed as

Alcohol OxidoreductasesCitrusLigninPlant ProteinsTranscription FactorsCold-Shock ResponseCold TemperatureGene Expression Regulation, PlantHomeostasisOxidation-ReductionReactive Oxygen SpeciesAlcohol Oxidoreductasescinnamyl alcohol dehydrogenaseLigninPlant ProteinsReactive Oxygen SpeciesTranscription FactorsCitrus ichangensiscold stresslignin biosynthesisRAP2ROS scavengingWRKY

Identifiers

PMID41249860
PMCPMC13140723

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Registered trials

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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.