Evidence map›Paper›PMID 42249328›Full record

ArticleBMC plant biology2026

Identification of the nsLTP gene family from sugar beet and functional analysis of BvnsLTP10 in drought tolerance.

Yanni Xu, Ronghua Shi, Ziqi Fan, Yingnan Mu, Yaqing Sun, Ningning Li, Shaoying Zhang, Guolong Li

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Article in BMC plant biology, 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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yanni XuCollege of Agriculture, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Ronghua ShiCollege of Agriculture, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Ziqi FanThe Second Forestry and Grassland Monitoring and Planning Institute of Inner Mongolia Autonomous Region, Ulanhot, 137400, China.
Yingnan MuInstitute of Crop Sciences, Inner Mongolia Academy of Agricultural and Animal Husbandry Sciences, Hohhot, Inner Mongolia, 010031, China.
Yaqing SunCollege of Agriculture, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Ningning LiCollege of Agriculture, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Shaoying ZhangCollege of Agriculture, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Guolong LiCollege of Agriculture, Inner Mongolia Agricultural University, Hohhot, 010018, China. lglg@imau.edu.cn.

Funding

Basic Research Funds for Universities in Inner Mongolia Autonomous Region BR220105National Natural Science Foundation of China 32460500The Earmarked Fund for CRAS-17 CRAS-17
6 · The paper itself

Abstract

Non-specific lipid transfer proteins (nsLTPs) participate in lipid-related processes and plant responses to abiotic stress, yet their roles in drought tolerance in sugar beet remain largely unclear. In this study, a genome-wide analysis identified 15 nsLTP genes in sugar beet, distributed across six chromosomes, and promoter analysis revealed multiple cis-acting elements associated with abiotic stress responses. Among these genes, BvnsLTP10 exhibits sustained up-regulation in leaves and peak induction in roots and stems under PEG-induced drought. Subcellular localization analysis showed that BvnsLTP10 is a secreted protein localized to the cell wall/apoplast, suggesting a role in extracellular lipid transport. Functional characterization in transgenic Arabidopsis demonstrated that BvnsLTP10 overexpression enhanced drought tolerance, as evidenced by increased fresh weight (1.85-fold), relative water content (1.41-fold), chlorophyll content (+ 36%), and Fv/Fm (+ 19.6%), along with elevated antioxidant enzyme activities (POD + 65.1%, SOD + 37.5%, CAT + 54.3%) and reduced electrolyte leakage (- 17.63%). SEM observations indicated potential changes in leaf and stem surface structures, and coordinated upregulation of wax biosynthesis and transport genes (KCS1, CER1, CER3, WSD1, FAR3, ABCG11; ~ 20-40-fold) under drought stress, suggesting a possible involvement of wax-related pathways. These findings indicate that BvnsLTP10 enhances drought tolerance by improving plant water status, strengthening antioxidant defense systems, and promoting extracellular structural modifications. Notably, the functional validation was conducted in Arabidopsis thaliana rather than sugar beet, which may limit direct functional extrapolation to the crop species. Nevertheless, BvnsLTP10 represents a promising candidate gene for future studies aimed at enhancing drought resilience in sugar beet.

Indexed as

Beta vulgarisCarrier ProteinsPlant ProteinsArabidopsisDrought ResistanceDroughtsGene Expression Regulation, PlantGenes, PlantMultigene FamilyPlants, Genetically ModifiedStress, PhysiologicalCarrier Proteinslipid transfer proteinPlant ProteinsBeta vulgaris L.BvnsLTP gene familyDroughtTransgenic Arabidopsis

Identifiers

PMID42249328
PMCPMC13459284

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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.