Base Flipping by MTERF1 Can Accommodate Multiple Conformations and Occurs in a Stepwise Fashion. Issue 12 (19th June 2016)

• Record Type: Journal Article
• Authors: Byrnes, James; Hauser, Kevin; Norona, Leah; Mejia, Edison; Simmerling, Carlos; Garcia-Diaz, Miguel
• Is Part Of: Journal of molecular biology. Volume 428:Issue 12(2016:Jun. 19)
• Page Start: 2542
• Page End: 2556
• Publication Date: 2016-06-19
• Subjects: EDTA ethylenediaminetetraacetic acid -- NSLS National Synchrotron Light Source -- HSP heavy strand promoter -- HS heavy strand -- LS light strand -- MTERF mitochondrial transcription termination factor -- RFY R162A, F243A, Y288A; mitochondria -- transcription termination -- X-ray crystallography -- molecular dynamics -- base flipping; Molecular biology -- Periodicals; Biology -- Periodicals; Biochemistry -- Periodicals; Bacteriology -- Periodicals; Molecular Biology -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biologie -- Périodiques; Biochimie -- Périodiques; Moleculaire biologie; Biochemistry; Biology; Molecular biology; Periodicals; 572.805
• DOI: 10.1016/j.jmb.2015.10.021
• Languages: English
• ISSNs: 0022-2836

Abstract

Abstract: Human mitochondrial transcription termination occurs within the leu-tRNA gene and is mediated by the DNA binding protein MTERF1. The crystal structure of MTERF1 bound to the canonical termination sequence reveals a rare base flipping event that involves the eversion of three nucleotides. These nucleotides are stabilized by stacking interactions with three MTERF1 residues, which are essential not only for base flipping but also for termination activity. To further understand the mechanism of base flipping, we examined each of the individual stacking interactions in structural, energetic and functional detail. Individual substitutions of Arg162, Tyr288 and Phe243 have revealed unequal contributions to overall termination activity. Furthermore, our work identifies an important role for Phe322 in the base flipping mechanism and we demonstrate how Phe322 and Phe243 are important for coupling base flipping between the heavy and light strand DNA chains. We propose a stepwise model for the base flipping process that recapitulates our observations. Finally, we show that MTERF1 has the ability to accommodate alternate active conformations. The adaptability of base flipping has implications for MTERF1 function and for the putative function of MTERF1 at alternative binding sites in human mitochondria. Graphical Abstract: Highlights: MTERF1 mediates a complex three-base flipping process stabilized by stacking interactions. Phe322 and Phe243 act as wedge residues preparing the DNA for flipping. The mechanism of flipping three nucleotides occurs in a stepwise manner. Perturbations to the stepwise mechanism alter MTERF1 termination ability.