The Drosophila melanogaster enzyme glycerol-3-phosphate dehydrogenase 1 is required for oogenesis, embryonic development, and amino acid homeostasis.

Autor: Rai M; Department of Biology, Indiana University, Bloomington, IN 47405, USA., Carter SM; Department of Biology, Indiana University, Bloomington, IN 47405, USA., Shefali SA; Department of Biology, Indiana University, Bloomington, IN 47405, USA., Mahmoudzadeh NH; Department of Biology, Indiana University, Bloomington, IN 47405, USA., Pepin R; Department of Chemistry, Indiana University, Bloomington, IN 47405, USA., Tennessen JM; Department of Biology, Indiana University, Bloomington, IN 47405, USA.
Jazyk: angličtina
Zdroj: G3 (Bethesda, Md.) [G3 (Bethesda)] 2022 Jul 29; Vol. 12 (8).
DOI: 10.1093/g3journal/jkac115
Abstrakt: As the fruit fly, Drosophila melanogaster, progresses from one life stage to the next, many of the enzymes that compose intermediary metabolism undergo substantial changes in both expression and activity. These predictable shifts in metabolic flux allow the fly meet stage-specific requirements for energy production and biosynthesis. In this regard, the enzyme glycerol-3-phosphate dehydrogenase 1 (GPDH1) has been the focus of biochemical genetics studies for several decades and, as a result, is one of the most well-characterized Drosophila enzymes. Among the findings of these earlier studies is that GPDH1 acts throughout the fly lifecycle to promote mitochondrial energy production and triglyceride accumulation while also serving a key role in maintaining redox balance. Here, we expand upon the known roles of GPDH1 during fly development by examining how depletion of both the maternal and zygotic pools of this enzyme influences development, metabolism, and viability. Our findings not only confirm previous observations that Gpdh1 mutants exhibit defects in larval development, lifespan, and fat storage but also reveal that GPDH1 serves essential roles in oogenesis and embryogenesis. Moreover, metabolomics analysis reveals that a Gpdh1 mutant stock maintained in a homozygous state exhibits larval metabolic defects that significantly differ from those observed in the F1 mutant generation. Overall, our findings highlight unappreciated roles for GPDH1 in early development and uncover previously undescribed metabolic adaptations that could allow flies to survive the loss of this key enzyme.
(© The Author(s) 2022. Published by Oxford University Press on behalf of Genetics Society of America.)
Databáze: MEDLINE
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