Abstract
Trehalose is the major insect hemolymph sugar and plays a diverse role. Its level is regulated endogenously by the dynamics of biosynthesis and distribution by sugar transporters (STs). The metabolic trade-off between trehalose synthesis and uptake remains poorly understood, despite its critical role in homeostasis. Here, we examined the role of a gut-specific trehalose transporter, HaST46 , in regulating this metabolic trade-off in Helicoverpa armigera , a Lepidopteran pest model. Integrated transcriptomics analysis and functional analyses revealed that HaST46 acts as a diet-responsive transporter, localised to the posterior midgut, with trehalose preference. Its expression is modulated in response to dietary trehalose availability, enhancing the efficient exogenous trehalose uptake while attenuating its endogenous synthesis and conserving energy. Functional perturbation through overexpression and silencing revealed a feedback-regulated mechanism in which HaST46 expression showed strong correlation with trehalose metabolising enzymes and other HaSTs isoforms to maintain systemic trehalose homeostasis. Overall, our findings reveal a metabolic trade-off between exogenous trehalose uptake and endogenous synthesis mediated by gut-specific sugar transporters.
Full text
1,444 characters
· extracted from
oa-doi-fallback
· click to expand
Abstract
Trehalose is the major insect hemolymph sugar and plays a diverse role. Its level is regulated endogenously by the dynamics of biosynthesis and distribution by sugar transporters (STs). The metabolic trade-off between trehalose synthesis and uptake remains poorly understood, despite its critical role in homeostasis. Here, we examined the role of a gut-specific trehalose transporter, HaST46, in regulating this metabolic trade-off in Helicoverpa armigera, a Lepidopteran pest model. Integrated transcriptomics analysis and functional analyses revealed that HaST46 acts as a diet-responsive transporter, localised to the posterior midgut, with trehalose preference. Its expression is modulated in response to dietary trehalose availability, enhancing the efficient exogenous trehalose uptake while attenuating its endogenous synthesis and conserving energy. Functional perturbation through overexpression and silencing revealed a feedback-regulated mechanism in which HaST46 expression showed strong correlation with trehalose metabolising enzymes and other HaSTs isoforms to maintain systemic trehalose homeostasis. Overall, our findings reveal a metabolic trade-off between exogenous trehalose uptake and endogenous synthesis mediated by gut-specific sugar transporters.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
1. Author order is revised 2. Supplementary information has been uploaded
Text is read by the "Ask this paper" AI Q&A widget below.
Extraction quality varies by source — PMC NXML preserves structure
cleanly, OA-HTML may include some navigation residue, and OA-PDF can
have broken hyphenation. The publisher copy
(via DOI)
is the canonical version.