Evidence map›Paper›PMID 42389138›Full record

ArticleFrontiers in plant science2026

Bioinformatic analysis, expression analysis, and subcellular localization of GeBP transcriptional regulator family in response to abiotic stress in

Sana Basharat, Wajid Saeed, Pingwu Liu, Muhammad Waseem

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Article in Frontiers in plant science, 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sana Basharat *School of Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), School of Tropical Agriculture and Forestry, Hainan University, Sanya, China.
Wajid SaeedSchool of Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), School of Tropical Agriculture and Forestry, Hainan University, Sanya, China.
Pingwu LiuSchool of Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), School of Tropical Agriculture and Forestry, Hainan University, Sanya, China.
Muhammad Waseem *School of Breeding and Multiplication (Sanya Institute of Breeding and Multiplication), School of Tropical Agriculture and Forestry, Hainan University, Sanya, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The GLABROUS1 enhancer-binding protein (GeBP) gene family represents a plant-specific class of transcriptional regulators involved in plant growth, development, and adaptation to environmental stresses. Although GeBP proteins have been characterized in Methods: In this study, we performed a genome-wide identification and characterization of GeBP genes in B. napus. Chromosomal distribution, phylogenetic relationships, gene duplication events, exonintron organization, conserved domains, promoter cis-regulatory elements, tissue-specific expression patterns, subcellular localization, and stress-responsive expression profiles under salt, drought, heat, and cold stresses were analyzed. Results: A total of 35 BnaGeBP proteins were identified and found to be unevenly distributed across the B. napus chromosomes. Phylogenetic analysis classified the BnaGeBP proteins into three distinct groups together with GeBP homologs from selected monocot and dicot species. Duplication analysis indicated that the expansion of the BnaGeBP family was mainly driven by segmental duplication events, with 20 segmental duplication pairs and one tandem duplication pair identified. Gene structure and conserved domain analyses supported the phylogenetic conservation of BnaGeBP genes. Promoter analysis revealed diverse hormone- and stress-responsive cis-regulatory elements, including drought- and low-temperature-responsive motifs. Tissue expression profiling showed variable spatial expression patterns, while selected BnaGeBP genes displayed differential expression under salt, drought (PEG6000), heat, and cold stress treatments. Discussion: This comprehensive analysis provides valuable insights into the evolution, structural conservation, and potential functions of the BnaGeBP gene family in

Indexed as

abiotic stressBnaGeBPBrassica napusphylogenyspatiotemporal expression

Identifiers

PMID42389138
PMCPMC13318797

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