Cargando…

Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP

H/ACA RNP complexes change uridines to pseudouridines in target non-coding RNAs in eukaryotes and archaea. H/ACA RNPs are comprised of a guide RNA and four essential proteins: Cbf5 (pseudouridine synthase), L7Ae, Gar1 and Nop10 in archaea. The guide RNA captures the target RNA via two antisense elem...

Descripción completa

Detalles Bibliográficos
Autores principales: Youssef, Osama A., Terns, Rebecca M., Terns, Michael P.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2094053/
https://www.ncbi.nlm.nih.gov/pubmed/17855403
http://dx.doi.org/10.1093/nar/gkm673
_version_ 1782138207948767232
author Youssef, Osama A.
Terns, Rebecca M.
Terns, Michael P.
author_facet Youssef, Osama A.
Terns, Rebecca M.
Terns, Michael P.
author_sort Youssef, Osama A.
collection PubMed
description H/ACA RNP complexes change uridines to pseudouridines in target non-coding RNAs in eukaryotes and archaea. H/ACA RNPs are comprised of a guide RNA and four essential proteins: Cbf5 (pseudouridine synthase), L7Ae, Gar1 and Nop10 in archaea. The guide RNA captures the target RNA via two antisense elements brought together to form a contiguous binding site within the pseudouridylation pocket (internal loop) of the guide RNA. Cbf5 and L7Ae interact independently with the guide RNA, and here we have examined the impacts of these proteins on the RNA in nucleotide protection assays. The results indicate that the interactions observed in a fully assembled H/ACA RNP are established in the sub-complexes, but also reveal a unique Cbf5–guide RNA interaction that is displaced by L7Ae. In addition, the results indicate that L7Ae binding at the kink (k)-turn of the guide RNA induces the formation of the upper stem, and thus also the pseudouridylation pocket. Our findings indicate that L7Ae is essential for formation of the substrate RNA binding site in the archaeal H/ACA RNP, and suggest that k-turn-binding proteins may remodel partner RNAs with important effects distant from the protein-binding site.
format Text
id pubmed-2094053
institution National Center for Biotechnology Information
language English
publishDate 2007
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-20940532007-12-03 Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP Youssef, Osama A. Terns, Rebecca M. Terns, Michael P. Nucleic Acids Res Molecular Biology H/ACA RNP complexes change uridines to pseudouridines in target non-coding RNAs in eukaryotes and archaea. H/ACA RNPs are comprised of a guide RNA and four essential proteins: Cbf5 (pseudouridine synthase), L7Ae, Gar1 and Nop10 in archaea. The guide RNA captures the target RNA via two antisense elements brought together to form a contiguous binding site within the pseudouridylation pocket (internal loop) of the guide RNA. Cbf5 and L7Ae interact independently with the guide RNA, and here we have examined the impacts of these proteins on the RNA in nucleotide protection assays. The results indicate that the interactions observed in a fully assembled H/ACA RNP are established in the sub-complexes, but also reveal a unique Cbf5–guide RNA interaction that is displaced by L7Ae. In addition, the results indicate that L7Ae binding at the kink (k)-turn of the guide RNA induces the formation of the upper stem, and thus also the pseudouridylation pocket. Our findings indicate that L7Ae is essential for formation of the substrate RNA binding site in the archaeal H/ACA RNP, and suggest that k-turn-binding proteins may remodel partner RNAs with important effects distant from the protein-binding site. Oxford University Press 2007-09 2007-09-12 /pmc/articles/PMC2094053/ /pubmed/17855403 http://dx.doi.org/10.1093/nar/gkm673 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Youssef, Osama A.
Terns, Rebecca M.
Terns, Michael P.
Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
title Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
title_full Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
title_fullStr Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
title_full_unstemmed Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
title_short Dynamic interactions within sub-complexes of the H/ACA pseudouridylation guide RNP
title_sort dynamic interactions within sub-complexes of the h/aca pseudouridylation guide rnp
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2094053/
https://www.ncbi.nlm.nih.gov/pubmed/17855403
http://dx.doi.org/10.1093/nar/gkm673
work_keys_str_mv AT youssefosamaa dynamicinteractionswithinsubcomplexesofthehacapseudouridylationguidernp
AT ternsrebeccam dynamicinteractionswithinsubcomplexesofthehacapseudouridylationguidernp
AT ternsmichaelp dynamicinteractionswithinsubcomplexesofthehacapseudouridylationguidernp