Different respiratory-defective phenotypes of Neurospora crassa and Saccharomyces cerevisiae after inactivation of the gene encoding the mitochondrial acyl carrier protein

Curr Genet. 1995 Dec;29(1):10-7. doi: 10.1007/BF00313188.

Abstract

The nuclear genes (acp-1, ACP1) encoding the mitochondrial acyl carrier protein were disrupted in Neurospora crassa and Saccharomyces cerevisiae. In n. crassa acp-1 is a peripheral subunit of the respiratory NADH : ubiquinone oxidoreductase (complex I). S. cerevisiae lacks complex I and its ACP1 appears to be located in the mitochondrial matrix. The loss of acp-1 in N. crassa causes two biochemical lesions. Firstly, the peripheral part of complex I is not assembled, and the membrane part is not properly assembled. The respiratory ubiquinol : cytochrome c oxidoreductase (complex III) and cytochrome c oxidase (complex IV) are made in normal amounts. Secondly, the lysophospholipid content of mitochondrial membranes is increased four-fold. In S. cerevisiae, the loss of ACP1 leads to a pleiotropic respiratory deficient phenotype.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyl Carrier Protein / genetics*
  • Acyl Carrier Protein / isolation & purification
  • Base Sequence
  • Electron Transport Complex I
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Gene Expression Regulation, Fungal
  • Mitochondria / chemistry
  • Mitochondria / genetics*
  • Molecular Sequence Data
  • Mutagenesis
  • NADH, NADPH Oxidoreductases / genetics
  • Neurospora crassa / genetics*
  • Neurospora crassa / growth & development
  • Phenotype
  • Phospholipids / biosynthesis
  • Phospholipids / chemistry
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / growth & development

Substances

  • Acyl Carrier Protein
  • Phospholipids
  • NADH, NADPH Oxidoreductases
  • Electron Transport Complex IV
  • Electron Transport Complex I

Associated data

  • GENBANK/X83578