Evidence map›Paper›PMID 40025443›Full record

ArticleBMC plant biology2025

Genomic signatures of SnRKs highlighted conserved evolution within orchids and stress responses through ABA signaling in the Cymbidium ensifolium.

Ruiyue Zheng, Kai Zhao, Jiemin Chen, Xuanyi Zhu, Yukun Peng, Mingli Shen, Zhong-Jian Liu, Donghui Peng, Yuzhen Zhou

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

9 authors.

Ruiyue Zheng *Ornamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Kai Zhao *College of Life Sciences, Fujian Normal University, Fuzhou, 350117, China.
Jiemin ChenOrnamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Xuanyi ZhuOrnamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Yukun PengOrnamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Mingli ShenCollege of Life Sciences, Fujian Normal University, Fuzhou, 350117, China.
Zhong-Jian LiuOrnamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Donghui PengOrnamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Yuzhen ZhouOrnamental Plant Germplasm Resources Innovation & Engineering Application Research Center, Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, College of Landscape Architecture and Art, The Cross-Strait Scientific and Technological Innovation Hub of Flower Industry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. zhouyuzhencn@fafu.edu.cn.

Funding

National Key Research and Development Program of China 2023YFD1600504
6 · The paper itself

Abstract

Sucrose non-fermenting 1-related protein kinases (SnRKs) are crucial for modulating plant responses to abiotic stresses, linking metabolism with stress signaling pathways. Investigating the roles and stress responses of SnRKs in plants paves the way for developing stress-tolerant strategies in orchid species. Here, 362 SnRK members were identified from nine current orchid genomes, highlighting the conservation of these genes in evolution. Among these, 33 CeSnRKs were found across 20 chromosomes of C. ensifolium genome. Multiple duplication events increased the complexity of CeSnRKs during independent evolution. Moreover, distinct functional domains beyond the kinase domain differentiated the subfamilies. These multi-copy members existed tissue specific expressions falling into 6 main trends, especially CeSnRK1, CeCIPK9, CeCIPK23 displayed a strict floral expression. ABA-related elements were enriched in the promoters of CeSnRKs, and stress-related miRNA binding sites were identified on partial CeSnRKs. Consequently, most CeSnRKs exhibited up-regulated expression during ABA treatment. Several genes, such as CeSnRK2.1 and CeCIPK28 involved growth and development at different times and various tissues. The up-regulation of SnRK2.1, along with high expression of SnRK1 and CIPK27 under drought stress, and the differential expression patterns of CeSnRKs under cold stress, underscore the involvement of CeSnRK genes in different stress responses. Additionally, the diverse interactions of CeSnRKs with proteins highlighted a multifaceted functional network.These findings offer valuable insights for the future functional characterization formation of CeSnRKs and the adaptive evolution of genes in orchids.

Indexed as

Abscisic AcidOrchidaceaePlant ProteinsProtein Serine-Threonine KinasesEvolution, MolecularGene Expression Regulation, PlantGenome, PlantPhylogenySignal TransductionStress, PhysiologicalAbscisic AcidPlant ProteinsProtein Serine-Threonine KinasesABA responseAbiotic stressEvolutionExpression patternsOrchidaceae

Identifiers

PMID40025443
PMCPMC11874761

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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.