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Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions

It is said that “hindsight is 20-20,” so, given the current year, it is an opportune time to review and learn from experiences studying long noncoding RNAs. Investigation of the Saccharomyces cerevisiae telomerase RNA, TLC1, has unveiled striking flexibility in terms of both structural and functiona...

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Autor principal: Zappulla, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356895/
https://www.ncbi.nlm.nih.gov/pubmed/32545864
http://dx.doi.org/10.3390/molecules25122750
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author Zappulla, David C.
author_facet Zappulla, David C.
author_sort Zappulla, David C.
collection PubMed
description It is said that “hindsight is 20-20,” so, given the current year, it is an opportune time to review and learn from experiences studying long noncoding RNAs. Investigation of the Saccharomyces cerevisiae telomerase RNA, TLC1, has unveiled striking flexibility in terms of both structural and functional features. Results support the “flexible scaffold” hypothesis for this 1157-nt telomerase RNA. This model describes TLC1 acting as a tether for holoenzyme protein subunits, and it also may apply to a plethora of RNAs beyond telomerase, such as types of lncRNAs. In this short perspective review, I summarize findings from studying the large yeast telomerase ribonucleoprotein (RNP) complex in the hope that this hindsight will sharpen foresight as so many of us seek to mechanistically understand noncoding RNA molecules from vast transcriptomes.
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spelling pubmed-73568952020-07-22 Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions Zappulla, David C. Molecules Review It is said that “hindsight is 20-20,” so, given the current year, it is an opportune time to review and learn from experiences studying long noncoding RNAs. Investigation of the Saccharomyces cerevisiae telomerase RNA, TLC1, has unveiled striking flexibility in terms of both structural and functional features. Results support the “flexible scaffold” hypothesis for this 1157-nt telomerase RNA. This model describes TLC1 acting as a tether for holoenzyme protein subunits, and it also may apply to a plethora of RNAs beyond telomerase, such as types of lncRNAs. In this short perspective review, I summarize findings from studying the large yeast telomerase ribonucleoprotein (RNP) complex in the hope that this hindsight will sharpen foresight as so many of us seek to mechanistically understand noncoding RNA molecules from vast transcriptomes. MDPI 2020-06-14 /pmc/articles/PMC7356895/ /pubmed/32545864 http://dx.doi.org/10.3390/molecules25122750 Text en © 2020 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zappulla, David C.
Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions
title Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions
title_full Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions
title_fullStr Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions
title_full_unstemmed Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions
title_short Yeast Telomerase RNA Flexibly Scaffolds Protein Subunits: Results and Repercussions
title_sort yeast telomerase rna flexibly scaffolds protein subunits: results and repercussions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356895/
https://www.ncbi.nlm.nih.gov/pubmed/32545864
http://dx.doi.org/10.3390/molecules25122750
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