Molecular Mechanisms of Insect-Resistant Function in Leaf Glandular Hairs of Different Wild Hazel Species Revealed by Integrated Transcriptomic and Metabolomic Analysis

Yingju Tian1,6,7

Qin Zhang1

Rui Han1

Mengna Xiao3

Zhiying Wu1

Wenli Li2

Ying Zhang2

Yuan Zhang2,5, Email

Dexin Wang1,2,4,5,6,7, Email

1College of Landscape Architecture and Horticulture, Southwest Forestry University, Kunming, Yunnan, 650224, China
2College of Forestry, Southwest Forestry University, Kunming, Yunnan, 650224, China
3Zhangjiajie Institute of Agricultural Science and Technology, Zhangjiajie, Yunnan, 427000, China
4Graduate School of Southwest Forestry University, Kunming, Yunnan, 650224, China
5Engineering Research Center for the Development and Utilization of Forest Resources in the Field of Big Health in Yunnan Provincial Universities, Kunming, Yunnan, 650224, China
6Key Laboratory of National Forestry and Grassland Administration on Lake Wetland Ecosystem Protection and Restoration, Kunming, Yunnan, 650224, China
7Shangri-La Potatso National Park Bita Lake Plateau Wetland Ecosystem Observation and Research Station of Yunnan Province, Kunming, Yunnan, 650233, China

 

Abstract

As an important economic forest tree species, hazel exhibits remarkable insect resistance in natural environments, with leaf glandular trichomes likely serving as key physical and chemical defense barriers. However, the molecular mechanisms underlying this insect resistance remain poorly understood. This study selected three wild hazel variants (E5, E7, and ED) displaying distinct glandular trichome morphologies and integrated transcriptomic and non-targeted metabolomic approaches to systematically analyze gene expression and metabolite accumulation in leaf glandular trichomes. Results revealed substantial interspecific variations in glandular trichome morphology, density, chemical composition, and metabolic pathways among the three variants. E5 exhibited high trichome density with pale purple pigmentation. Although key flavonoid biosynthesis genes were significantly upregulated, flavanol accumulation remained low, whereas pronounced accumulation of kaempferol suggested a metabolic redirection mechanism. In contrast, E7 and ED displayed lower trichome density and a transparent appearance. Despite reduced expression of flavonoid pathway genes, both accumulated substantial flavanols and related compounds, indicating a constitutive storage strategy. Galactose metabolism analysis further revealed distinct carbon allocation strategies among variants to support insect resistance. This study demonstrates that flavonoid and galactose metabolic pathways play pivotal roles in regulating insect resistance in hazel leaf glandular trichomes, providing a theoretical basis for understanding insect resistance mechanisms in forest trees and supporting resistance breeding efforts.

Molecular Mechanisms of Insect-Resistant Function in Leaf Glandular Hairs of Different Wild Hazel Species Revealed by Integrated Transcriptomic and Metabolomic Analysis