Mitochondrial transcription termination factor 1 directs polar replication fork pausing

Nucleic Acids Res. 2016 Jul 8;44(12):5732-42. doi: 10.1093/nar/gkw302. Epub 2016 Apr 25.

Abstract

During replication of nuclear ribosomal DNA (rDNA), clashes with the transcription apparatus can cause replication fork collapse and genomic instability. To avoid this problem, a replication fork barrier protein is situated downstream of rDNA, there preventing replication in the direction opposite rDNA transcription. A potential candidate for a similar function in mitochondria is the mitochondrial transcription termination factor 1 (MTERF1, also denoted mTERF), which binds to a sequence just downstream of the ribosomal transcription unit. Previous studies have shown that MTERF1 prevents antisense transcription over the ribosomal RNA genes, a process which we here show to be independent of the transcription elongation factor TEFM. Importantly, we now demonstrate that MTERF1 arrests mitochondrial DNA (mtDNA) replication with distinct polarity. The effect is explained by the ability of MTERF1 to act as a directional contrahelicase, blocking mtDNA unwinding by the mitochondrial helicase TWINKLE. This conclusion is also supported by in vivo evidence that MTERF1 stimulates TWINKLE pausing. We conclude that MTERF1 can direct polar replication fork arrest in mammalian mitochondria.

MeSH terms

  • Basic-Leucine Zipper Transcription Factors / genetics*
  • Basic-Leucine Zipper Transcription Factors / metabolism
  • DNA Helicases / genetics*
  • DNA Helicases / metabolism
  • DNA Replication*
  • DNA, Mitochondrial / genetics*
  • DNA, Mitochondrial / metabolism
  • DNA, Ribosomal / genetics*
  • DNA, Ribosomal / metabolism
  • HEK293 Cells
  • Humans
  • Mitochondria / genetics*
  • Mitochondria / metabolism
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • RNA, Ribosomal / genetics
  • RNA, Ribosomal / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Basic-Leucine Zipper Transcription Factors
  • DNA, Mitochondrial
  • DNA, Ribosomal
  • MTERF1 protein, human
  • Mitochondrial Proteins
  • RNA, Ribosomal
  • TEFM protein, human
  • Transcription Factors
  • DNA Helicases
  • TWNK protein, human