Stunning Intricacies of <scp>RNA</scp> Editing Complexes <scp>RECC</scp> , <scp>RESC</scp> , and <scp>REH2C</scp> : Functional Organization, Developmental Regulation, and Evolutionary History in Kinetoplastid Protists

RNA metabolism in kinetoplastid protists (Kinetoplastea), including trypanosomes and Leishmania, involves unique post-transcriptional mitochondrial RNA editing that creates translatable mRNAs through uridine (U) insertions and deletions (U-indels) directed by antisense guide RNAs (gRNAs). Like other biological processes that require specific RNA targeting, this system faces several challenges beyond coordinating its many components: assembling mRNA-gRNA hybrids, recognizing hundreds of sites, and accurately distinguishing pre-edited, partially edited, and fully edited transcripts in the mitochondrial environment. In parasites such as Trypanosoma brucei, significant energetic adaptations to different host environments also involve critical editing changes during development. The editing holoenzyme includes three molecular complexes and isoforms that carry most proteins: RNA Editing Catalytic Complexes (RECCs), which catalyze U-indel cycles; RNA Editing Substrate Complexes (RESCs), which serve as scaffolds to coordinate the editing components; and the RNA Editing Helicase 2 Complex (REH2C), which contains key proteins involved in developmental editing regulation. However, more proteins and functions are being discovered. The editing system, best understood in T. brucei, shows considerable evolutionary conservation in its core machinery; however, it varies in the extent of RNA editing and the organization of mitochondrial mRNA and gRNA genes across different species. Here we explore recent progress in our understanding of RNA editing and the growing use of modern computational tools, including artificial intelligence (AI) and structural methods, to examine function, organization, developmental regulation, and evolutionary aspects of this amazing system. This article is categorized under: RNA Interactions with Proteins and Other Molecules > RNA-Protein Complexes RNA Processing > RNA Editing and Modification.

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Publication Details

Journal
Wiley Interdisciplinary Reviews - RNA
Published
2026-02-25
DOI
https://doi.org/10.1002/wrna.70037
Primary Topic
Trypanosoma species research and implications
Type
article
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0.00

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Stunning Intricacies of RNA Editing Complexes RECC , RESC , and REH2C : Functional Organization, Developmental Regulation, and Evolutionary History in Kinetoplastid Protists

Naghmeh Poorinmohammad, Sara L. Zimmer, Cody Goode, Ken Stuart et al.
Wiley Interdisciplinary Reviews - RNA
Trypanosoma species research and implications
article

Stunning Intricacies of RNA Editing Complexes RECC , RESC , and REH2C : Functional Organization, Developmental Regulation, and Evolutionary History in Kinetoplastid Protists

Naghmeh Poorinmohammad, Sara L. Zimmer, Cody Goode, Ken Stuart, Alasdair Ivens, Reza Salavati, Sunil Kumar Sharma, Jorge Cruz‐Reyes, Laurie K. Read, Jason Carnes, Kristína Záhonová, Nicholas J. Savill, Suzanne M. McDermott, Poorya Mirzavand Borujeni, Lars O'Hara, Dave Speijer, Achim Schnaufer, Julius Lukeš, Zihao Chen
article en

Abstract

RNA metabolism in kinetoplastid protists (Kinetoplastea), including trypanosomes and Leishmania, involves unique post-transcriptional mitochondrial RNA editing that creates translatable mRNAs through uridine (U) insertions and deletions (U-indels) directed by antisense guide RNAs (gRNAs). Like other biological processes that require specific RNA targeting, this system faces several challenges beyond coordinating its many components: assembling mRNA-gRNA hybrids, recognizing hundreds of sites, and accurately distinguishing pre-edited, partially edited, and fully edited transcripts in the mitochondrial environment. In parasites such as Trypanosoma brucei, significant energetic adaptations to different host environments also involve critical editing changes during development. The editing holoenzyme includes three molecular complexes and isoforms that carry most proteins: RNA Editing Catalytic Complexes (RECCs), which catalyze U-indel cycles; RNA Editing Substrate Complexes (RESCs), which serve as scaffolds to coordinate the editing components; and the RNA Editing Helicase 2 Complex (REH2C), which contains key proteins involved in developmental editing regulation. However, more proteins and functions are being discovered. The editing system, best understood in T. brucei, shows considerable evolutionary conservation in its core machinery; however, it varies in the extent of RNA editing and the organization of mitochondrial mRNA and gRNA genes across different species. Here we explore recent progress in our understanding of RNA editing and the growing use of modern computational tools, including artificial intelligence (AI) and structural methods, to examine function, organization, developmental regulation, and evolutionary aspects of this amazing system. This article is categorized under: RNA Interactions with Proteins and Other Molecules > RNA-Protein Complexes RNA Processing > RNA Editing and Modification.

Wiley Interdisciplinary Reviews - RNAVol. 17(2)
Sewanee: The University of the South (US), University of Alberta (CA), Royal Botanic Garden Edinburgh (GB), University of Ostrava (CZ), University of Washington (US), Charles University (CZ), University of South Bohemia in České Budějovice (CZ), Institute of Parasitology of the Slovak Academy of Sciences (SK), University of Minnesota, Duluth (US), Centre for Immunity, Infection and Evolution (GB), Ste. Anne's Hospital (CA), Amsterdam University Medical Centers (NL), McGill University (CA), University at Buffalo, State University of New York (US), Texas A&M University (US), University of Edinburgh (GB)
National Science Foundation, Dalhousie University, National Institutes of Health, Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada
Life in Land
Openalex Percentile: Top 40%
Trypanosoma species research and implications
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