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MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression.
McAdams, Natalie M; Harrison, Gregory L; Tylec, Brianna L; Ammerman, Michelle L; Chen, Runpu; Sun, Yijun; Read, Laurie K.
Afiliação
  • McAdams NM; Department of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York 14203, USA.
  • Harrison GL; Department of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York 14203, USA.
  • Tylec BL; Department of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York 14203, USA.
  • Ammerman ML; Department of Chemistry and Biochemistry, Kettering University, Flint, Michigan 48504, USA.
  • Chen R; Department of Computer Science and Engineering, University at Buffalo, Buffalo, New York 14260, USA.
  • Sun Y; Department of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York 14203, USA.
  • Read LK; Department of Microbiology and Immunology, University at Buffalo Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York 14203, USA.
RNA ; 25(9): 1177-1191, 2019 Sep.
Article em En | MEDLINE | ID: mdl-31221726
ABSTRACT
Uridine insertion deletion editing in kinetoplastid protozoa requires a complex machinery, a primary component of which is the RNA editing substrate binding complex (RESC). RESC contains two modules termed GRBC (guide RNA binding complex) and REMC (RNA editing mediator complex), although how interactions between these modules and their mRNA and gRNA binding partners are controlled is not well understood. Here, we demonstrate that the ARM/HEAT repeat containing RESC protein, MRB10130, controls REMC association with mRNA- and gRNA-loaded GRBC. High-throughput sequencing analyses show that MRB10130 functions in both initiation and 3' to 5' progression of editing through gRNA-defined domains. Editing intermediates that accumulate upon MRB10130 depletion significantly intersect those in cells depleted of another RESC organizer, MRB7260, but are distinct from those in cells depleted of specific REMC proteins. We present a model in which MRB10130 coordinates numerous protein-protein and protein-RNA interactions during editing progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Edição de RNA Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: RNA Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Edição de RNA Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: RNA Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos