Evidence map›Paper›PMID 42525917›Full record

ArticleMolecular biology and evolution2026

Parallel expansion of trehalose transporter genes integrates intestinal energy metabolism with developmental growth in lepidopteran insects.

Qingyu Lu, Yanyan Zhou, Yanting Liang, Wenhui Jing, Yinghui Li, Jingbo Zhao, Huabing Wang

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Article in Molecular biology and evolution, 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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5 · Who and what money

Authors and funding

7 authors.

Qingyu LuCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0009-0005-1932-1706
Yanyan ZhouCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0000-0002-8813-3777
Yanting LiangCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0000-0001-6152-7592
Wenhui JingCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0009-0004-4362-9375
Yinghui LiCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0000-0001-6512-9137
Jingbo ZhaoCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0009-0008-7517-7130
Huabing WangCollege of Animal Sciences, Zhejiang University, Hangzhou, Zhejiang, China.ORCID 0000-0002-6848-2590

Funding

National Natural Science Foundation of China 32170483National Natural Science Foundation of China 32570551Science Foundation of Zhejiang Province of China LQ23C040001Zhejiang Province Agricultural Technology Major Collaborative Promotion Project 2024ZDXT09Zhejiang Province Science and Technology Cooperation Program 2026SNJF053
6 · The paper itself

Abstract

Trehalose is the principal circulating sugar in insects, yet how diversification of its transport system contributes to metabolic adaptability is unclear. Here, comparative genomics across 194 insect species reveals recurrent expansion of the trehalose transporter Tret1, with Lepidoptera retaining a conserved tandem duplication that generated two paralogs, Tret1-1 and Tret1-2. Functional analyses suggest a differentiated functional relationship between them: BmTret1-1 is indispensable for systemic trehalose flux, midgut integrity, and larval growth, whereas BmTret1-2 is highly expressed in the brain and may serve as a compensatory paralog of BmTret1-1. By integrating multiomics, single-nucleus transcriptomics, and functional assays, we further show that loss of BmTret1-1 is associated with altered intestinal stem cell to enterocyte (EC) differentiation dynamics, accompanied by reduced EC abundance, thereby linking nutrient transport capacity to epithelial renewal and organismal growth. Together with the parallel expansion of trehalase genes, our findings reveal a general framework in which coordinated expansion and functional cooperation of the trehalose transport-catabolism axis contribute to metabolic homeostasis in Lepidoptera. This study offers novel insights into the evolution of insect trehalose metabolism.

Indexed as

Energy MetabolismInsect ProteinsLepidopteraMembrane Transport ProteinsTrehaloseAnimalsInsect ProteinsMembrane Transport ProteinsTrehalosegene expansionmetabolic adaptationparallel evolutiontrehalose

Identifiers

PMID42525917
PMCPMC13419077

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