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The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN

Human telomerase RNA (hTR) is transcribed as a precursor that is then posttranscriptionally modified and processed. A fraction of the transcripts is oligoadenylated by TRAMP and either processed into the mature hTR or degraded by the exosome. Here, we characterize the processing of 3′ extended forms...

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Autores principales: Tseng, Chi-Kang, Wang, Hui-Fang, Schroeder, Morgan R., Baumann, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303318/
https://www.ncbi.nlm.nih.gov/pubmed/30575725
http://dx.doi.org/10.1038/s41467-018-07822-6
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author Tseng, Chi-Kang
Wang, Hui-Fang
Schroeder, Morgan R.
Baumann, Peter
author_facet Tseng, Chi-Kang
Wang, Hui-Fang
Schroeder, Morgan R.
Baumann, Peter
author_sort Tseng, Chi-Kang
collection PubMed
description Human telomerase RNA (hTR) is transcribed as a precursor that is then posttranscriptionally modified and processed. A fraction of the transcripts is oligoadenylated by TRAMP and either processed into the mature hTR or degraded by the exosome. Here, we characterize the processing of 3′ extended forms of varying length by PARN and RRP6. We show that tertiary RNA interactions unique to the longer transcripts favor RNA degradation, whereas H/ACA RNP assembly stimulates productive processing. Interestingly, the H/ACA complex actively promotes processing in addition to protecting the mature 3′ end. Processing occurs in two steps with longer forms first being trimmed by RRP6 and shorter forms then being processed by PARN. These results reveal how RNA structure and RNP assembly affect the kinetics of processing and degradation and ultimately determine the amount of functional telomerase produced in cells.
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spelling pubmed-63033182018-12-23 The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN Tseng, Chi-Kang Wang, Hui-Fang Schroeder, Morgan R. Baumann, Peter Nat Commun Article Human telomerase RNA (hTR) is transcribed as a precursor that is then posttranscriptionally modified and processed. A fraction of the transcripts is oligoadenylated by TRAMP and either processed into the mature hTR or degraded by the exosome. Here, we characterize the processing of 3′ extended forms of varying length by PARN and RRP6. We show that tertiary RNA interactions unique to the longer transcripts favor RNA degradation, whereas H/ACA RNP assembly stimulates productive processing. Interestingly, the H/ACA complex actively promotes processing in addition to protecting the mature 3′ end. Processing occurs in two steps with longer forms first being trimmed by RRP6 and shorter forms then being processed by PARN. These results reveal how RNA structure and RNP assembly affect the kinetics of processing and degradation and ultimately determine the amount of functional telomerase produced in cells. Nature Publishing Group UK 2018-12-21 /pmc/articles/PMC6303318/ /pubmed/30575725 http://dx.doi.org/10.1038/s41467-018-07822-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tseng, Chi-Kang
Wang, Hui-Fang
Schroeder, Morgan R.
Baumann, Peter
The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN
title The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN
title_full The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN
title_fullStr The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN
title_full_unstemmed The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN
title_short The H/ACA complex disrupts triplex in hTR precursor to permit processing by RRP6 and PARN
title_sort h/aca complex disrupts triplex in htr precursor to permit processing by rrp6 and parn
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303318/
https://www.ncbi.nlm.nih.gov/pubmed/30575725
http://dx.doi.org/10.1038/s41467-018-07822-6
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