Cloning and Analysis of the Alternative Oxidase Gene of Neurospora crassa

Author:

Li Qiuhong1,Ritzel R Gary1,McLean Lesley L T1,McIntosh Lee2,Ko Tak3,Bertrand Helmut3,Nargang Frank E1

Affiliation:

1. Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E9

2. Department of Energy Plant Research Laboratory and Department of Biochemistry, Michigan State University, East Lansing, Michigan 48824-1312

3. Department of Microbiology, Michigan State University, East Lansing, Michigan 48824-1101

Abstract

Mitochondria of Neurospora crassa contain a cyanide-resistant alternative respiratory pathway in addition to the cytochrome pathway. The alternative oxidase is present only when electron flow through the cytochrome chain is restricted. Both genomic and cDNA copies for the alternative oxidase gene have been isolated and analyzed. The sequence of the predicted protein is homologous to that of other species. The mRNA for the alternative oxidase is scarce in wild-type cultures grown under normal conditions, but it is abundant in cultures grown in the presence of chloramphenicol, an inhibitor of mitochondrial protein synthesis, or in mutants deficient in mitochondrial cytochromes. Thus, induction of alternative oxidase appears to be at the transcriptional level. Restriction fragment length polymorphism mapping of the isolated gene demonstrated that it is located in a position corresponding to the aod-1 locus. Sequence analysis of mutant aod-1 alleles reveals mutations affecting the coding sequence of the alternative oxidase. The level of aod-1 mRNA in an aod-2 mutant strain that had been grown in the presence of chloramphenicol was reduced several fold relative to wild-type, supporting the hypothesis that the product of aod-2 is required for optimal expression of aod-1.

Publisher

Oxford University Press (OUP)

Subject

Genetics

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