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Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes

Uridylate insertion/deletion RNA editing in Trypanosoma brucei is a complex system that is not found in humans, so there is interest in targeting this system for drug development. This system uses hundreds of small non-coding guide RNAs (gRNAs) to modify the mitochondrial mRNA transcriptome. This pr...

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Autores principales: Kumar, Vikas, Doharey, Pawan K., Gulati, Shelly, Meehan, Joshua, Martinez, Mary G., Hughes, Karrisa, Mooers, Blaine H. M., Cruz-Reyes, Jorge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488192/
https://www.ncbi.nlm.nih.gov/pubmed/31034523
http://dx.doi.org/10.1371/journal.pone.0211525
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author Kumar, Vikas
Doharey, Pawan K.
Gulati, Shelly
Meehan, Joshua
Martinez, Mary G.
Hughes, Karrisa
Mooers, Blaine H. M.
Cruz-Reyes, Jorge
author_facet Kumar, Vikas
Doharey, Pawan K.
Gulati, Shelly
Meehan, Joshua
Martinez, Mary G.
Hughes, Karrisa
Mooers, Blaine H. M.
Cruz-Reyes, Jorge
author_sort Kumar, Vikas
collection PubMed
description Uridylate insertion/deletion RNA editing in Trypanosoma brucei is a complex system that is not found in humans, so there is interest in targeting this system for drug development. This system uses hundreds of small non-coding guide RNAs (gRNAs) to modify the mitochondrial mRNA transcriptome. This process occurs in holo-editosomes that assemble several macromolecular trans factors around mRNA including the RNA-free RNA editing core complex (RECC) and auxiliary ribonucleoprotein (RNP) complexes. Yet, the regulatory mechanisms of editing remain obscure. The enzymatic accessory RNP complex, termed the REH2C, includes mRNA substrates and products, the multi-domain 240 kDa RNA Editing Helicase 2 (REH2) and an intriguing 8-zinc finger protein termed REH2-Associated Factor 1 ((H2)F1). Both of these proteins are essential in editing. REH2 is a member of the DExH/RHA subfamily of RNA helicases with a conserved C-terminus that includes a regulatory OB-fold domain. In trypanosomes, (H2)F1 recruits REH2 to the editing apparatus, and (H2)F1 downregulation causes REH2 fragmentation. Our systematic mutagenesis dissected determinants in REH2 and (H2)F1 for the assembly of REH2C, the stability of REH2, and the RNA-mediated association of REH2C with other editing trans factors. We identified functional OB-fold amino acids in eukaryotic DExH/RHA helicases that are conserved in REH2 and that impact the assembly and interactions of REH2C. (H2)F1 upregulation stabilized REH2 in vivo. Mutation of the core cysteines or basic amino acids in individual zinc fingers affected the stabilizing property of (H2)F1 but not its interactions with other examined editing components. This result suggests that most, if not all, fingers may contribute to REH2 stabilization. Finally, a recombinant REH2 (240 kDa) established that the full-length protein is a bona fide RNA helicase with ATP-dependent unwinding activity. REH2 is the only DExH/RHA-type helicase in kinetoplastid holo-editosomes.
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spelling pubmed-64881922019-05-17 Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes Kumar, Vikas Doharey, Pawan K. Gulati, Shelly Meehan, Joshua Martinez, Mary G. Hughes, Karrisa Mooers, Blaine H. M. Cruz-Reyes, Jorge PLoS One Research Article Uridylate insertion/deletion RNA editing in Trypanosoma brucei is a complex system that is not found in humans, so there is interest in targeting this system for drug development. This system uses hundreds of small non-coding guide RNAs (gRNAs) to modify the mitochondrial mRNA transcriptome. This process occurs in holo-editosomes that assemble several macromolecular trans factors around mRNA including the RNA-free RNA editing core complex (RECC) and auxiliary ribonucleoprotein (RNP) complexes. Yet, the regulatory mechanisms of editing remain obscure. The enzymatic accessory RNP complex, termed the REH2C, includes mRNA substrates and products, the multi-domain 240 kDa RNA Editing Helicase 2 (REH2) and an intriguing 8-zinc finger protein termed REH2-Associated Factor 1 ((H2)F1). Both of these proteins are essential in editing. REH2 is a member of the DExH/RHA subfamily of RNA helicases with a conserved C-terminus that includes a regulatory OB-fold domain. In trypanosomes, (H2)F1 recruits REH2 to the editing apparatus, and (H2)F1 downregulation causes REH2 fragmentation. Our systematic mutagenesis dissected determinants in REH2 and (H2)F1 for the assembly of REH2C, the stability of REH2, and the RNA-mediated association of REH2C with other editing trans factors. We identified functional OB-fold amino acids in eukaryotic DExH/RHA helicases that are conserved in REH2 and that impact the assembly and interactions of REH2C. (H2)F1 upregulation stabilized REH2 in vivo. Mutation of the core cysteines or basic amino acids in individual zinc fingers affected the stabilizing property of (H2)F1 but not its interactions with other examined editing components. This result suggests that most, if not all, fingers may contribute to REH2 stabilization. Finally, a recombinant REH2 (240 kDa) established that the full-length protein is a bona fide RNA helicase with ATP-dependent unwinding activity. REH2 is the only DExH/RHA-type helicase in kinetoplastid holo-editosomes. Public Library of Science 2019-04-29 /pmc/articles/PMC6488192/ /pubmed/31034523 http://dx.doi.org/10.1371/journal.pone.0211525 Text en © 2019 Kumar et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kumar, Vikas
Doharey, Pawan K.
Gulati, Shelly
Meehan, Joshua
Martinez, Mary G.
Hughes, Karrisa
Mooers, Blaine H. M.
Cruz-Reyes, Jorge
Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes
title Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes
title_full Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes
title_fullStr Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes
title_full_unstemmed Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes
title_short Protein features for assembly of the RNA editing helicase 2 subcomplex (REH2C) in Trypanosome holo-editosomes
title_sort protein features for assembly of the rna editing helicase 2 subcomplex (reh2c) in trypanosome holo-editosomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488192/
https://www.ncbi.nlm.nih.gov/pubmed/31034523
http://dx.doi.org/10.1371/journal.pone.0211525
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