Evidence map›Paper›PMID 41540377›Full record

ArticleBMC plant biology2026

Genome-wide identification and analysis of the cysteine-rich transmembrane module genes in Chinese cabbage (Brassica rapa L. ssp. Pekinensis) and BrCYSTM1 is involved in leaf size development.

Han Zheng, Qun Liu, Tong Bu, Qian Zhang, Jingjuan Li, Yihui Zhang, Cheng Li, Lixia Wang, Fengde Wang, Jianwei Gao

Abstract read
In one paragraph

Article in BMC plant biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Han ZhengShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.
Qun LiuCollege of Life Science, Shandong Normal University, Jinan, 250100, China.
Tong BuCollege of Life Science, Shandong Normal University, Jinan, 250100, China.
Qian ZhangCollege of Life Science, Shandong Normal University, Jinan, 250100, China.
Jingjuan LiShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.
Yihui ZhangShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.
Cheng LiShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.
Lixia WangShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.
Fengde WangShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China.
Jianwei GaoShandong Key Laboratory of Bulk Open-field Vegetable Breeding, Ministry of Agriculture and Rural Affairs Key Laboratory of Huang Huai Protected Horticulture Engineering, Institute of Vegetables, Shandong Academy of Agricultural Sciences, Jinan, 250100, China. jianweigao3@qq.com.

Funding

Shandong Provincial Key Research and Development Program for International Sci-Tech Cooperation Projects 2024KJHZ005the "333" Talent Project of Shandong Academy of Agricultural Sciences CXGC2025F07the China Agriculture Research System CARS-23-G13the Modern Agricultural Industrial Technology System Funding of Shandong Province, China SDAIT-05the National Natural Science Foundation, China 32172591the Project of 20 New Items for Universities in Jinan, Shandong 202228058the Prospect of Shandong Seed Project, China 2023LZGC014
6 · The paper itself

Abstract

backgroundCysteine-rich transmembrane module (CYSTM) peptides are ubiquitous in eukaryotes and primarily involved in stress responses and defense mechanisms. To date, no comprehensive genomic identification of this family in Chinese cabbage has been reported, and the biological functions of the CYSTM genes in Chinese cabbage remain largely unexplored.

resultsNine members of the CYSTM family were identified in Chinese cabbage and was named according to their homologous genes in Arabidopsis. DNA structure and motif analyses revealed that the CYSTM family is highly conserved. Evolutionary analysis suggests that Chinese cabbage shares a more closely related lineage with other Brassicaceae species in comparison to Arabidopsis. Expression pattern analysis demonstrated that the BrCYSTM genes exhibit considerable variation across different tissues and display diverse expression patterns in response to various hormone treatments and abiotic stresses. Since leaf traits are directly associated with the yield of Chinese cabbage, and BrCYSTM1 exhibits the highest expression level in Chinese cabbage leaves, we conducted an array of in-depth studies on this gene. BrCYSTM1 undergoes self-association to form homodimer and also interacts with BrCYSTM10a or BrCYSTM10b to establish heterodimers. The Bimolecular Fluorescence Complementation (BiFC) assay demonstrated that these dimers are localized both in the cytoplasm and on the plasma membrane, suggesting their potential involvement in signal transduction processes. The overexpression of BrCYSTM1 in both Chinese cabbage and Arabidopsis significantly enlarged leaf size, with a similar effect observed in the AtCYSTM1 mutant background. These findings support the role of BrCYSTM1 in promoting leaf growth, indicating its potential involvement in regulating leaf size.

conclusionsOur results suggest that BrCYSTMs are involved in the response of plants to a variety of stresses. The role of BrCYSTM1 as a positive regulator of leaf development is well established in Arabidopsis, and its conserved function gains preliminary support from overexpression studies in Chinese cabbage.

Indexed as

Brassica rapaMembrane ProteinsPlant LeavesPlant ProteinsGene Expression Regulation, PlantGenes, PlantPhylogenyMembrane ProteinsPlant ProteinsAbiotic stressBrCYSTMChinese cabbageHomodimer or heterodimerLeaf size development

Identifiers

PMID41540377
PMCPMC12853963

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.