Mitochondrial plasmids of Neurospora: integration into mitochondrial DNA and evidence for reverse transcription in

Cell
|November 21, 1986
PubMed

Insights

Neurospora mitochondrial plasmids can cause growth defects by integrating into mitochondrial DNA. These suppressive plasmids, possibly generated by reverse transcription, lead to defective mitochondrial DNA in mutants.

Area of Science:

  • Molecular Biology
  • Mycology
  • Genetics

Background:

  • The Mauriceville and Varkud mitochondrial plasmids in Neurospora are circular DNA molecules.
  • Their genetic makeup suggests a link to mobile genetic elements like retrotransposons and introns.

Purpose of the Study:

  • To investigate the detrimental effects of these mitochondrial plasmids on Neurospora growth.
  • To characterize the molecular basis of plasmid-induced growth impairment.

Main Methods:

  • Isolation and characterization of Neurospora mutants exhibiting impaired growth due to plasmid activity.
  • Analysis of plasmid and mitochondrial DNA (mtDNA) sequences in mutant strains.
  • Investigation of plasmid structure, including insertions and integration sites.

Main Results:

  • Twelve mutants with impaired growth were identified, all harboring suppressive variant plasmids.
  • Ten of these mutants also showed defective mitochondrial DNA (mtDNA).
  • Suppressive plasmids contained insertions, often including tRNA sequences, near the 5' RNA start site, suggesting reverse transcription involvement.
  • Mitochondrial plasmid sequences were found integrated into the mtDNA of at least three mutants, with junctions indicative of RNA-mediated integration.

Conclusions:

  • The study demonstrates that Neurospora mitochondrial plasmids can exhibit detrimental behavior, leading to impaired growth and defective mtDNA.
  • The findings suggest a mechanism involving RNA intermediates and reverse transcription in the generation and integration of these suppressive plasmids.
  • These plasmids represent a unique example of mobile genetic elements impacting host mitochondrial genome integrity.

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