Helix unwinding and base flipping enable human MTERF1 to terminate mitochondrial transcription.

ABSTRACT: Defects in mitochondrial gene expression are associated with aging and disease. Mterf proteins have been implicated in modulating transcription, replication and protein synthesis. We have solved the structure of a member of this family, the human mitochondrial transcriptional terminator MTERF1, bound to dsDNA containing the termination sequence. The structure indicates that upon sequence recognition MTERF1 unwinds the DNA molecule, promoting eversion of three nucleotides. Base flipping is critical for stable binding and transcriptional termination. Additional structural and biochemical results provide insight into the DNA binding mechanism and explain how MTERF1 recognizes its target sequence. Finally, we have demonstrated that the mitochondrial pathogenic G3249A and G3244A mutations inter

SUBMITTER: Yakubovskaya E 

PROVIDER: S-EPMC2887341 | biostudies-literature | 2010 Jun

REPOSITORIES: biostudies-literature