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bioRxiv · 10.1101/2025.01.07.631819

Hypoxia-inducible factor 1α is required to establish the larval glycolytic program in Drosophila melanogaster

Heidarian, Y.·Fasteen, T. D.·Mungcal, L.·Buddika, K.·Mahmoudzadeh, N. H.·Nemkov, T.·D'Alessandro, A.·Tennessen, J.
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Abstract

The rapid growth that occurs during Drosophila larval development requires a dramatic rewiring of central carbon metabolism to support biosynthesis. Larvae achieve this metabolic state, in part, by coordinately up-regulating the expression of genes involved in carbohydrate metabolism. The resulting metabolic program exhibits hallmark characteristics of aerobic glycolysis and establishes a physiological state that supports growth. To date, the only factor known to activate the larval glycolytic program is the Drosophila Estrogen-Related Receptor (dERR). However, dERR is dynamically regulated during the onset of this metabolic switch, indicating that other factors must be involved. Here we discover that Sima, the Drosophila ortholog of Hif1, is also essential for establishing the larval glycolytic program. Using a multi-omics approach, we demonstrate that sima mutants fail to properly activate aerobic glycolysis and die during larval development with metabolic defects that phenocopy dERR mutants. Moreover, we demonstrate that dERR and Sima/Hif1 protein accumulation is mutually dependent, as loss of either transcription factor results in decreased abundance of the other protein. Considering that the mammalian homologs of ERR and Hif1 also cooperatively regulate aerobic glycolysis in cancer cells, our findings establish the fly as a powerful genetic model for studying the interaction between these two key metabolic regulators. STRUCTURED ABSTRACTO_ST_ABSObjectivesC_ST_ABSThe rapid growth that occurs during Drosophila larval development requires a dramatic rewiring of central carbon metabolism to support biosynthesis. Larvae achieve this metabolic state, in part, by coordinately up-regulating the expression of genes involved in carbohydrate metabolism. The resulting metabolic program exhibits hallmark characteristics of aerobic glycolysis and establishes a physiological state that supports growth. To date, the only factor known to activate the larval glycolytic program is the Drosophila Estrogen-Related Receptor (dERR). However, dERR is dynamically regulated during the onset of this metabolic switch, indicating that other factors must be involved. Here we examine the possibility the Drosophila ortholog of Hypoxia inducible factor 1 (Hif1) is also required to activate the larval glycolytic program. MethodsCRISPR/Cas9 was used to generate new loss-of-function alleles in the Drosophila gene similar (sima), which encodes the sole fly ortholog of Hif1. The resulting mutant strains were analyzed using a combination of metabolomics and RNAseq for defects in carbohydrate metabolism. ResultsOur studies reveal that sima mutants fail to activate aerobic glycolysis and die during larval development with metabolic phenotypes that mimic those displayed by dERR mutants. Moreover, we demonstrate that dERR and Sima/Hif1 protein accumulation is mutually dependent, as loss of either transcription factor results in decreased abundance the other protein. ConclusionsThese findings demonstrate that Sima/HIF1 is required during embryogenesis to coordinately up-regulate carbohydrate metabolism in preparation for larval growth. Notably, our study also reveals that the Sima-dependent gene expression profile shares considerable overlap with that observed in dERR mutant, suggesting that Sima/HIF1 and dERR cooperatively regulate embryonic and larval glycolytic gene expression. HIGHLIGHTSO_LIThe Drosophila melanogaster gene similar (sima), which encodes the sole fly ortholog of Hif1, is required to up-regulate glycolysis in preparation for larval growth. C_LIO_LIsima mutant larvae exhibit severe defects in carbohydrate metabolism and die during the second larval instar. C_LIO_LIsima mutant larvae exhibit the same metabolic phenotypes as Drosophila Estrogen Related Receptor (dERR) mutants, suggesting that these two transcription factors coordinately regulate the larval glycolytic program. C_LIO_LISima/Hif1 and dERR accumulation is mutually dependent, as loss of either transcription factor results in decreased abundance of the other. C_LI

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Heidarian, Y., Fasteen, T. D., Mungcal, L., Buddika, K., Mahmoudzadeh, N. H., Nemkov, T., D'Alessandro, A., Tennessen, J.. 2025-01-08. Hypoxia-inducible factor 1α is required to establish the larval glycolytic program in Drosophila melanogaster. https://doi.org/10.1101/2025.01.07.631819

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