4.6 Article

Role of trehalose phosphate synthase in anoxia tolerance and development in Drosophila melanogaster

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 277, Issue 5, Pages 3274-3279

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M109479200

Keywords

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Funding

  1. NHLBI NIH HHS [R01 HL066327, R01-HL66327] Funding Source: Medline
  2. NICHD NIH HHS [P01 HD032573, P01-HD32573] Funding Source: Medline
  3. NINDS NIH HHS [R01-NS35918] Funding Source: Medline

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Recent studies have shown that trehalose plays a protective role in yeast in a variety of stresses, including heat, freezing and thawing, dehydration, hyperosmotic shock, and oxidant injury. Because (a) heat shock and anoxia share mechanisms that allow organisms to survive, (b) Drosophila melanogaster is tolerant to anoxia, and (c) trehalose is present in flies and is metabolically active, we asked whether trehalose can protect against anoxic stress. Here we report on a new role of trehalose in anoxia resistance in Drosophila. We first cloned the gene trehalose-6-phosphate synthase (tps1), which synthesizes trehalose, and examined the effect of tpsl overexpression as well as mutation on the resistance of Drosophila to anoxia. Upon induction of tpsl, trehalose increased, and this was associated with increased tolerance to anoxia. Furthermore, in vitro experiments showed that trehalose reduced protein aggregation caused by anoxia. Homozygous tpsl mutant (P-element insertion into the third intron of the gene) leads to lethality at an early larval stage, and excision of the P-element rescues totally the phenotype. We conclude that trehalose contributes to anoxia tolerance in flies; this protection is likely to be due to a reduction of protein aggregation.

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