Evidence map›Paper›PMID 41199156›Full record

ArticleBMC genomics2025

Genome-wide identification and expression analysis of the PYL gene family in response to salt, drought and cold stresses in Solanum melongena L.

Fangyi Gong, Yanhong Lan, Tian Zhang, Chun Li, Yifan Li, Feng Xia, Xiaojun Liu, Duchen Liu, Genyun Liang, Chao Fang and 1 more

Abstract read
In one paragraph

Article in BMC genomics, 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. Genome-Wide Analysis of theInternational 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

11 authors.

Fangyi GongSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Yanhong LanSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Tian ZhangSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Chun LiSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Yifan LiSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Feng XiaSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Xiaojun LiuSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Duchen LiuSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Genyun LiangSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China.
Chao FangSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China. saasfangchao@163.com.
Peng CaiSichuan Provincial Key Laboratory of Fruit and Vegetable Horticultural Crop Germplasm Innovation and Utilization, Horticulture Institute, Sichuan Academy of Agricultural Sciences, Chengdu, 610066, China. cp215@163.com.

Funding

Sichuan Innovation Team Program of CARS SCCXTD-2024-5Sichuan Province Engineering Technology Research Center of Vegetables 2023PZSC0301Sichuan Provincial Science and Technology Plan Project 2021YFYZ0010Sichuan Provincial Science and Technology Plan Project 2021YFYZ0022the 1+9 Program of SAAS 1+9KJGG03
6 · The paper itself

Abstract

backgroundEggplant (Solanum melongena L.) is a globally important vegetable crop, yet its production faces challenges due to various abiotic stresses. PYL proteins, which act as crucial abscisic acid (ABA) receptors, play a pivotal role in the plant's response to abiotic stresses. However, a genome-wide analysis of the PYL gene family in eggplant has not been conducted to date, hindering the study of their functions in plant development and their roles in abiotic stress tolerance.

resultsThis study presents the first genome-wide identification of the PYL gene family in eggplant (Solanum melongena) (Sm-PYL), revealing 24 Sm-PYL genes (Sm-PYL1-24) encoding proteins with lengths (92-722 aa), molecular weights (10,256.59-83,087.82 Da), and isoelectric points (4.45-9.77), classified into three subfamilies (I-III). Structural analysis showed exon numbers (1-11) and 15 conserved motifs, while evolutionary analysis identified six syntenic gene pairs under strong purifying selection (Ka/Ks < 0.22) and expansion through diverse duplication mechanisms. Comparative genomics with tomato, potato and pepper revealed 86 syntenic pairs (Ka/Ks < 0.50). Promoter analysis uncovered 20 cis-regulatory elements, predominantly light-responsive, associated with stress, hormone signaling, and growth. Expression profiling implicated Sm-PYL1/12/14/15/23 in salt/drought responses and Sm-PYL7/9/10/13/16/23/24 in cold adaptation, providing insights into their functional diversification in eggplant.

conclusionThis study presents the first genome-wide identification of 24 Sm-PYL genes in eggplant, classified into three subfamilies. Structural and evolutionary analyses revealed conserved motifs, purifying selection, and gene family expansion through duplication. Comparative genomics with tomato, potato and pepper identified 86 syntenic pairs, highlighting evolutionary conservation. Promoter analysis uncovered stress- and hormone-related cis-elements, while expression profiling linked specific Sm-PYLs to salt/drought (Sm-PYL1/12/14/15/23) and cold (Sm-PYL7/9/10/13/16/23/24) responses. These findings enhance understanding of ABA-mediated stress tolerance in eggplant and provide a basis for future functional studies to improve abiotic stress resilience.

Indexed as

Cold-Shock ResponseMultigene FamilyPlant ProteinsSolanum melongenaStress, PhysiologicalDroughtsGene Expression ProfilingGene Expression Regulation, PlantGenome, PlantGenome-Wide Association StudyPhylogenyPlant ProteinsABAAbiotic stressExpressionPYLSolanum melongena

Identifiers

PMID41199156
PMCPMC12593932

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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.