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Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network
Dynamic regulation of RNA folding and structure is critical for the biogenesis and function of RNAs and ribonucleoprotein (RNP) complexes. Through their nucleotide triphosphate-dependent remodelling functions, RNA helicases are key modulators of RNA/RNP structure. While some RNA helicases are dedica...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458436/ https://www.ncbi.nlm.nih.gov/pubmed/35993807 http://dx.doi.org/10.1093/nar/gkac687 |
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author | Bohnsack, Katherine E Kanwal, Nidhi Bohnsack, Markus T |
author_facet | Bohnsack, Katherine E Kanwal, Nidhi Bohnsack, Markus T |
author_sort | Bohnsack, Katherine E |
collection | PubMed |
description | Dynamic regulation of RNA folding and structure is critical for the biogenesis and function of RNAs and ribonucleoprotein (RNP) complexes. Through their nucleotide triphosphate-dependent remodelling functions, RNA helicases are key modulators of RNA/RNP structure. While some RNA helicases are dedicated to a specific target RNA, others are multifunctional and engage numerous substrate RNAs in different aspects of RNA metabolism. The discovery of such multitasking RNA helicases raises the intriguing question of how these enzymes can act on diverse RNAs but also maintain specificity for their particular targets within the RNA-dense cellular environment. Furthermore, the identification of RNA helicases that sit at the nexus between different aspects of RNA metabolism raises the possibility that they mediate cross-regulation of different cellular processes. Prominent and extensively characterized multifunctional DEAH/RHA-box RNA helicases are DHX15 and its Saccharomyces cerevisiae (yeast) homologue Prp43. Due to their central roles in key cellular processes, these enzymes have also served as prototypes for mechanistic studies elucidating the mode of action of this type of enzyme. Here, we summarize the current knowledge on the structure, regulation and cellular functions of Prp43/DHX15, and discuss the general concept and implications of RNA helicase multifunctionality. |
format | Online Article Text |
id | pubmed-9458436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94584362022-09-09 Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network Bohnsack, Katherine E Kanwal, Nidhi Bohnsack, Markus T Nucleic Acids Res Critical Reviews and Perspectives Dynamic regulation of RNA folding and structure is critical for the biogenesis and function of RNAs and ribonucleoprotein (RNP) complexes. Through their nucleotide triphosphate-dependent remodelling functions, RNA helicases are key modulators of RNA/RNP structure. While some RNA helicases are dedicated to a specific target RNA, others are multifunctional and engage numerous substrate RNAs in different aspects of RNA metabolism. The discovery of such multitasking RNA helicases raises the intriguing question of how these enzymes can act on diverse RNAs but also maintain specificity for their particular targets within the RNA-dense cellular environment. Furthermore, the identification of RNA helicases that sit at the nexus between different aspects of RNA metabolism raises the possibility that they mediate cross-regulation of different cellular processes. Prominent and extensively characterized multifunctional DEAH/RHA-box RNA helicases are DHX15 and its Saccharomyces cerevisiae (yeast) homologue Prp43. Due to their central roles in key cellular processes, these enzymes have also served as prototypes for mechanistic studies elucidating the mode of action of this type of enzyme. Here, we summarize the current knowledge on the structure, regulation and cellular functions of Prp43/DHX15, and discuss the general concept and implications of RNA helicase multifunctionality. Oxford University Press 2022-08-22 /pmc/articles/PMC9458436/ /pubmed/35993807 http://dx.doi.org/10.1093/nar/gkac687 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Critical Reviews and Perspectives Bohnsack, Katherine E Kanwal, Nidhi Bohnsack, Markus T Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network |
title | Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network |
title_full | Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network |
title_fullStr | Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network |
title_full_unstemmed | Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network |
title_short | Prp43/DHX15 exemplify RNA helicase multifunctionality in the gene expression network |
title_sort | prp43/dhx15 exemplify rna helicase multifunctionality in the gene expression network |
topic | Critical Reviews and Perspectives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458436/ https://www.ncbi.nlm.nih.gov/pubmed/35993807 http://dx.doi.org/10.1093/nar/gkac687 |
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