PfKsgA1 functions as a transcription initiation factor and interacts with the N-terminal region of the mitochondrial RNA polymerase of Plasmodium falciparum

• Published in: International journal for parasitology Vol. 51; no. 1; pp. 23 - 37
• Main Authors: Gupta, Ankit, Shrivastava, Deepti, Shakya, Anil Kumar, Gupta, Kirti, Pratap, JV, Habib, Saman
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01-01-2021
• Subjects: KsgA1; Malaria; Mitochondria; RNA polymerase; Transcription factor; KsgA1; Mitochondria; RNA polymerase; Malaria; Transcription factor
• ISSN: 0020-7519; 1879-0135
• DOI: 10.1016/j.ijpara.2020.07.010

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•Phage-like polymerase PfmtRNAP targets to the Plasmodium mitochondrion and interacts with mtDNA.•PfmtRNAP interacts with PfKsgA1, the latter serving as a transcription initiation factor.•The N-ter of PfmtRNAP primarily contacts the PfKsgA1 C-ter domain with some contacts made with the N-ter.•Mitochondrial PfKsgA1 has a dual function, as a ribosome biogenesis protein and as a transcription factor.
The small mitochondrial genome (mtDNA) of the malaria parasite is known to transcribe its genes polycistonically, although promoter element(s) have not yet been identified. An unusually large Plasmodium falciparum candidate mitochondrial phage-like RNA polymerase (PfmtRNAP) with an extended N-terminal region is encoded by the parasite nuclear genome. Using specific antibodies against the enzyme, we established that PfmtRNAP was targeted exclusively to the mitochondrion and interacted with mtDNA. Phylogenetic analysis showed that it is part of a separate apicomplexan clade. A search for PfmtRNAP-associated transcription initiation factors using sequence homology and in silico protein–protein interaction network analysis identified PfKsgA1. PfKsgA1 is a dual cytosol- and mitochondrion-targeted protein that functions as a small subunit rRNA dimethyltransferase in ribosome biogenesis. Chromatin immunoprecipitation showed that PfKsgA1 interacts with mtDNA, and in vivo crosslinking and pull-down experiments confirmed PfmtRNAP-PfKsgA1 interaction. The ability of PfKsgA1 to serve as a transcription initiation factor was demonstrated by complementation of yeast mitochondrial transcription factor Mtf1 function in Rpo41-driven in vitro transcription. Pull-down experiments using PfKsgA1 and PfmtRNAP domains indicated that the N-terminal region of PfmtRNAP interacts primarily with the PfKsgA1 C-terminal domain with some contacts being made with the linker and N-terminal domain of PfKsgA1. In the absence of full-length recombinant PfmtRNAP, solution structures of yeast mitochondrial RNA polymerase Rpo41 complexes with Mtf1 or PfKsgA1 were determined by small-angle X-ray scattering. Protein interaction interfaces thus identified matched with those reported earlier for Rpo41-Mtf1 interaction and overlaid with the PfmtRNAP-interfacing region identified experimentally for PfKsgA1. Our results indicate that in addition to a role in mitochondrial ribosome biogenesis, PfKsgA1 has an independent function as a transcription initiation factor for PfmtRNAP.