Abstract

Mitochondrial RNA polymerases depend on initiation factors, such as TFB2M in humans and Mtf1 in yeast Saccharomyces cerevisiae, for promoter-specific transcription. These factors drive the melting of promoter DNA, but how they support RNA priming and growth was not understood. We show that the flexible C-terminal tails of Mtf1 and TFB2M play a crucial role in RNA priming by aiding template strand alignment in the active site for high-affinity binding of the initiating nucleotides. Using single-molecule fluorescence approaches, we show that the Mtf1 C-tail promotes RNA growth during initiation by stabilizing the scrunched DNA conformation. Additionally, due to its location in the path of the nascent RNA, the C-tail of Mtf1 serves as a sensor of the RNA–DNA hybrid length. Initially, steric clashes of the Mtf1 C-tail with short RNA–DNA hybrids cause abortive synthesis but clashes with longer RNA-DNA trigger conformational changes for the timely release of the promoter DNA to commence the transition into elongation. The remarkable similarities in the functions of the C-tail and σ3.2 finger of the bacterial factor suggest mechanistic convergence of a flexible element in the transcription initiation factor that engages the DNA template for RNA priming and growth and disengages when needed to generate the elongation complex.

Highlights

  • The mitochondrial genomes of eukaryotes are transcribed by RNA polymerases (RNAPs) that are distinct from nuclear RNAPs and homologous to single-subunit bacteriophage T7/T3 RNAP [1]

  • Our studies show that the Ctail regions of Mitochondrial Transcription Factor 1 (Mtf1) and Transcription Factor B2 mitochondrial (TFB2M) are critical for RNA priming and growth

  • The human and yeast mitochondrial RNAPs rely on transcription initiation factors, Mtf1 and TFB2M, respectively, for promoter-specific transcription initiation

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Summary

Introduction

The mitochondrial genomes of eukaryotes are transcribed by RNA polymerases (RNAPs) that are distinct from nuclear RNAPs and homologous to single-subunit bacteriophage T7/T3 RNAP [1]. Mtf and TFB2M are evolutionarily related to RNA methyltransferases, but as transcription initiation factors, they facilitate promoter-specific transcription initiation [3,6,7,8,9]. Both initiation factors drive the melting of the promoter DNA by binding to the non-template strand and trapping the melted strand in their nucleic acid binding pocket [10,11,12,13]. The C-tail of TFB2M contacts the intercalating ␤-hairpin and the thumb domain of POLRMT and is positioned in the path of the nascent RNA

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