Evidence map›Paper›PMID 40375071›Full record

ArticleBMC plant biology2025

Genome-wide identification, tissue expression pattern, and salt stress response analysis of the NAC gene family in Thinopyrum elongatum.

Jilin Sun, Xiaokuo Cui, Jiaqi Zhang, Fansen Meng, Jiangong Li, Shenghui Zhou, Changai Wu, Peng Zhou, Silong Sun, Long Han

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 4 papers.

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4citing papers in PubMed
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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Jilin Sun *National Key Laboratory of Wheat Improvement, College of Agronomy, Shandong Agricultural University, Tai 'an, Shandong, 271018, China.
Xiaokuo Cui *National Key Laboratory of Wheat Improvement, Shandong Engineering Research Center of Plant-Microbial Restoration for Saline-Alkali Land, College of Life Sciences, Shandong Agricultural University, Tai 'an, 271018, China.
Jiaqi ZhangNational Key Laboratory of Wheat Improvement, College of Agronomy, Shandong Agricultural University, Tai 'an, Shandong, 271018, China.
Fansen MengNational Key Laboratory of Wheat Improvement, College of Agronomy, Shandong Agricultural University, Tai 'an, Shandong, 271018, China.
Jiangong LiNational Key Laboratory of Wheat Improvement, College of Agronomy, Shandong Agricultural University, Tai 'an, Shandong, 271018, China.
Shenghui ZhouNational Key Facility of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Changai WuNational Key Laboratory of Wheat Improvement, Shandong Engineering Research Center of Plant-Microbial Restoration for Saline-Alkali Land, College of Life Sciences, Shandong Agricultural University, Tai 'an, 271018, China.
Peng ZhouNational Key Facility of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Silong SunNational Key Laboratory of Wheat Improvement, College of Agronomy, Shandong Agricultural University, Tai 'an, Shandong, 271018, China.
Long HanTai 'an Academy of Agricultural Sciences, Tai 'an, Shandong, 271000, China. hanlonghello2008@163.com.

Funding

The Key R&D Program of Shandong Province, China 2023LZGC022
6 · The paper itself

Abstract

backgroundThe NAC (NAM, ATAF1/2, and CUC2) gene family plays a critical role in regulating plant growth, developmental processes, and stress response mechanisms. While NAC genes have been systematically characterized in multiple plant species, this study focused on genome-wide identification of NAC family members in Thinopyrum elongatum (designated as TeNACs) through integrated bioinformatics approaches. Comprehensive analyses were conducted to determine the physicochemical characteristics, conserved motifs, gene structure, phylogenetic relationships, chromosomal collinearity, and expression profiles of the identified TeNACs. This multi-dimensional characterization provides fundamental insights into the structural and functional diversity of NAC transcription factors in Th. elongatum.

resultsA total of 116 NAC transcription factors were systematically identified in Th. elongatum, distributed across all seven chromosomes. Comprehensive physicochemical characterization revealed substantial variation among TeNAC proteins: amino acid length (162-718 aa), molecular weight (18.33-78.25 kDa), isoelectric point (6.5-7.5), instability index (30.34-63.32), and aliphatic index (50.92-80.68). Hydropathicity analysis confirmed the hydrophilic nature of all TeNACs, with grand average values consistently below zero. Conserved motif profiling demonstrated a highly conserved architecture in TeNACs, featuring ordered arrangements of motifs 3, 4, 1, 5, 6, 2, and 7. Phylogenetic reconstruction classified TeNACs into 14 distinct clades through comparative analysis with Arabidopsis thaliana NAC genes, notably lacking ANAC001 and OsNAC8 homologs. Comparative genomic analysis identified significant syntenic conservation between TeNACs and wheat NAC genes. Protein interaction network prediction indicated intricate functional associations among TeNAC proteins. Computational predictions coupled with experimental validation of TeNAC021 confirmed exclusive nuclear localization for all family members. Differential expression analysis across a salt gradient (0-300 mM) identified 14 TeNACs with progressive up-regulation and 5 showing consistent down-regulation. RT-qPCR confirmed salt-responsive expression patterns for eight TeNACs demonstrating marked transcriptional changes.

conclusionsThis systematic investigation establishes a robust theoretical framework for subsequent structural and functional characterization of TeNACs in Th. elongatum.

Indexed as

Multigene FamilyPlant ProteinsPoaceaeSalt StressTranscription FactorsGene Expression Regulation, PlantGenes, PlantGenome, PlantPhylogenyPlant ProteinsTranscription FactorsExpression patternSalt stressTeNACsTh. elongatum

Identifiers

PMID40375071
PMCPMC12080115

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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.