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MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression
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 interac...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800514/ https://www.ncbi.nlm.nih.gov/pubmed/31221726 http://dx.doi.org/10.1261/rna.071902.119 |
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author | McAdams, Natalie M. Harrison, Gregory L. Tylec, Brianna L. Ammerman, Michelle L. Chen, Runpu Sun, Yijun Read, Laurie K. |
author_facet | McAdams, Natalie M. Harrison, Gregory L. Tylec, Brianna L. Ammerman, Michelle L. Chen, Runpu Sun, Yijun Read, Laurie K. |
author_sort | McAdams, Natalie M. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6800514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68005142020-09-01 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. RNA Article 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. Cold Spring Harbor Laboratory Press 2019-09 /pmc/articles/PMC6800514/ /pubmed/31221726 http://dx.doi.org/10.1261/rna.071902.119 Text en © 2019 McAdams et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Article McAdams, Natalie M. Harrison, Gregory L. Tylec, Brianna L. Ammerman, Michelle L. Chen, Runpu Sun, Yijun Read, Laurie K. MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression |
title | MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression |
title_full | MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression |
title_fullStr | MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression |
title_full_unstemmed | MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression |
title_short | MRB10130 is a RESC assembly factor that promotes kinetoplastid RNA editing initiation and progression |
title_sort | mrb10130 is a resc assembly factor that promotes kinetoplastid rna editing initiation and progression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800514/ https://www.ncbi.nlm.nih.gov/pubmed/31221726 http://dx.doi.org/10.1261/rna.071902.119 |
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