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
Summary
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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