Evidence map›Paper›PMID 41718788›Full record

ArticlePlant cell reports2026

Overexpression of DWARF14-LIKE2 in Arabidopsis thaliana alters multiple traits related to plant morphology and osmotic and salt stress tolerance.

Xiaofan Nie, Liangliang Li, Chenbo Zhu, Kaixin Yang, Qingtian Li, Jiahe Fu, Minghui Xing, Mingming Wang, David C Nelson, Xianzhong Feng and 6 more

Abstract read
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Article in Plant cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

16 authors.

Xiaofan Nie *State Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Liangliang Li *State Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Chenbo ZhuState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Kaixin YangState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Qingtian LiYazhouwan National Laboratory, 572025, Sanya, Hainan, China.
Jiahe FuCollege of Life Sciences, Northeast Forestry University, 150040, Harbin, Heilongjiang, China.
Minghui XingState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Mingming WangState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
David C NelsonDepartment of Botany and Plant Sciences, University of California, 92521, Riverside, CA, USA.
Xianzhong FengState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Jiuhai ZhaoState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Zhengwei LiangState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Chunjie TianState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China.
Lam-Son Phan TranInstitute of Genomics for Crop Abiotic Stress Tolerance, Department of Plant and Soil Science, Texas Tech University, 79409, Lubbock, TX, USA. son.tran@ttu.edu.
Xiaojian YinState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China. yinxiaojian@iga.ac.cn.
Weiqiang LiState Key Laboratory of Black Soils Conservation and Utilization, Jilin Da'an Agro-Ecosystem National Observation and Research Station, Changchun Jingyuetan Remote Sensing Experiment Station, Northeast Institute of Geography and Agroecology, Chinese Academy of Sciences, 130102, Changchun, Jilin, China. liweiqiang@iga.ac.cn.

Funding

National Key Research and Development Program of China 2022YFD1500505the Strategic Priority Research Program of the Chinese Academy of Sciences XDA28110100This work was supported by the Natural Science Foundation of China 32370321
6 · The paper itself

Abstract

Karrikin signaling, mediated by the KARRIKIN INSENSITIVE 2 (KAI2) receptor, promotes seed germination, inhibits hypocotyl elongation, regulates root architecture, and mitigates abiotic stresses in plants. DWARF14-LIKE2 (DLK2), encoding a close homolog of KAI2, has been considered a marker gene in karrikin signaling pathway. However, the biological roles of DLK2 in plant growth, development, and abiotic stress responses are still unknown. Here, we found that DLK2 disruption significantly decreased hypocotyl elongation and cotyledon angle, while increasing root hair development and rosette leaf downward-curving. These phenotypes of dlk2 mutants are opposite to those observed in DLK2-overexpressing (DLK2-OE) plants. Furthermore, DLK2-OE plants showed significantly induced seed dormancy but reduced growth of cotyledon, rosette leaves, and primary and lateral roots in young seedlings. At later developmental stage, DLK2-OE plants displayed significantly reduced flowering and shoot branching, while showing increased stem diameter, final rosette and petal size, and seed size and weight. Transcriptome analysis of DLK2-OE leaves revealed that cell cycle, cell division, responses to abiotic stresses, and plant hormone pathways are regulated by DLK2. Consistently, DLK2-OE plants exhibited significantly smaller palisade mesophyll cell size, larger cell size in seed surface, and enhanced performance under osmotic and salt stresses. These findings demonstrate that DLK2 plays important roles in regulating plant growth and development, as well as plant stress responses, as their homologs KAI2 and D14, although with diverse functions in some growth-related traits.

Indexed as

ArabidopsisArabidopsis ProteinsReceptors, Cell SurfaceSalt ToleranceGene Expression Regulation, PlantGerminationHypocotylOsmotic PressurePhenotypePlant LeavesPlant RootsPlants, Genetically ModifiedSalt StressSeedsArabidopsis ProteinsReceptors, Cell SurfaceAbiotic stressesCell divisionKarrikinPlant growth and developmentStrigolactoneTranscriptome

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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.