Mutation in pre-mRNA adenosine deaminase markedly attenuates neuronal tolerance to O2 deprivation in Drosophila melanogaster.

Abstract

O2 deprivation can produce many devastating clinical conditions such as myocardial infarct and stroke. The molecular mechanisms underlying the inherent tissue susceptibility or tolerance to O2 lack are, however, not well defined. Since the fruit fly, Drosophila melanogaster, is extraordinarily tolerant to O2 deprivation, we have performed a genetic screen in the Drosophila to search for loss-of-function mutants that are sensitive to low O2. Here we report on the genetic and molecular characterization of one of the genes identified from this screen, named hypnos-2. This gene encodes a Drosophila pre-mRNA adenosine deaminase (dADAR) and is expressed almost exclusively in the adult central nervous system. Disruption of the dADAR gene results in totally unedited sodium (Para), calcium (Dmca1A), and chloride (DrosGluCl-alpha) channels, a very prolonged recovery from anoxic stupor, a vulnerability to heat shock and increased O2 demands, and neuronal degeneration in aged flies. These data clearly demonstrate that, through the editing of ion channels as targets, dADAR, for which there are mammalian homologues, is essential for adaptation to altered environmental stresses such as O2 deprivation and for the prevention of premature neuronal degeneration.

• Authors: E Ma, X Q Gu, X Wu, T Xu, G G Haddad
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 107 Issue 6 Pg. 685-93 (Mar 2001) ISSN: 0021-9738 [Print] United States
• PMID: 11254668 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• DNA Primers
• RNA-Binding Proteins
• ADARB1 protein, human
• Adenosine Deaminase
• Oxygen

Topics

• Adenosine Deaminase (genetics)
• Amino Acid Sequence
• Animals
• Animals, Genetically Modified
• Base Sequence
• Chromosome Mapping
• DNA Primers (genetics)
• Disease Models, Animal
• Drosophila melanogaster (genetics, metabolism)
• Female
• Genes, Insect
• Genetic Complementation Test
• Humans
• Hypoxia (genetics, physiopathology)
• In Situ Hybridization
• Male
• Molecular Sequence Data
• Mutation
• Neurons (metabolism)
• Oxygen (metabolism)
• RNA-Binding Proteins
• Reverse Transcriptase Polymerase Chain Reaction
• Sequence Homology, Amino Acid