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Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs

MicroRNAs (miRNAs) and small interfering RNAs (siRNAs) are loaded into Argonaute (AGO) proteins, forming RNA-induced silencing complexes (RISCs). The assembly process establishes the seed, central, 3′ supplementary, and tail regions across the loaded guide, enabling the RISC to recognize and cleave...

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Autores principales: Sim, GeunYoung, Kehling, Audrey C., Park, Mi Seul, Divoky, Cameron, Zhang, Huaqun, Malhotra, Nipun, Secor, Jackson, Nakanishi, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634876/
https://www.ncbi.nlm.nih.gov/pubmed/37961191
http://dx.doi.org/10.1101/2023.10.27.564437
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author Sim, GeunYoung
Kehling, Audrey C.
Park, Mi Seul
Divoky, Cameron
Zhang, Huaqun
Malhotra, Nipun
Secor, Jackson
Nakanishi, Kotaro
author_facet Sim, GeunYoung
Kehling, Audrey C.
Park, Mi Seul
Divoky, Cameron
Zhang, Huaqun
Malhotra, Nipun
Secor, Jackson
Nakanishi, Kotaro
author_sort Sim, GeunYoung
collection PubMed
description MicroRNAs (miRNAs) and small interfering RNAs (siRNAs) are loaded into Argonaute (AGO) proteins, forming RNA-induced silencing complexes (RISCs). The assembly process establishes the seed, central, 3′ supplementary, and tail regions across the loaded guide, enabling the RISC to recognize and cleave target RNAs. This guide segmentation is caused by anchoring the 3′ end at the AGO PAZ domain, but the minimum guide length required for the conformation remains to be studied because there was no method by which to do so. Using a 3′→5′ exonuclease ISG20, we determined the lengths of AGO-associated miR-20a and let-7a with 3′ ends that no longer reach the PAZ domain. Unexpectedly, miR-20a and let-7a needed different lengths, 19 and 20 nt, respectively, to maintain their RISC conformation. This difference can be explained by the low affinity of the PAZ domain for the adenosine at g19 of let-7a, suggesting that the tail-region sequence slightly alters the minimum guide length. We also present that 17-nt guides are sufficiently short enough to function as tinyRNAs (tyRNAs) whose 3’ ends are not anchored at the PAZ domain. Since tyRNAs do not have the prerequisite anchoring for the standardized guide segmentation, they would recognize targets differently from miRNAs and siRNAs.
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spelling pubmed-106348762023-11-13 Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs Sim, GeunYoung Kehling, Audrey C. Park, Mi Seul Divoky, Cameron Zhang, Huaqun Malhotra, Nipun Secor, Jackson Nakanishi, Kotaro bioRxiv Article MicroRNAs (miRNAs) and small interfering RNAs (siRNAs) are loaded into Argonaute (AGO) proteins, forming RNA-induced silencing complexes (RISCs). The assembly process establishes the seed, central, 3′ supplementary, and tail regions across the loaded guide, enabling the RISC to recognize and cleave target RNAs. This guide segmentation is caused by anchoring the 3′ end at the AGO PAZ domain, but the minimum guide length required for the conformation remains to be studied because there was no method by which to do so. Using a 3′→5′ exonuclease ISG20, we determined the lengths of AGO-associated miR-20a and let-7a with 3′ ends that no longer reach the PAZ domain. Unexpectedly, miR-20a and let-7a needed different lengths, 19 and 20 nt, respectively, to maintain their RISC conformation. This difference can be explained by the low affinity of the PAZ domain for the adenosine at g19 of let-7a, suggesting that the tail-region sequence slightly alters the minimum guide length. We also present that 17-nt guides are sufficiently short enough to function as tinyRNAs (tyRNAs) whose 3’ ends are not anchored at the PAZ domain. Since tyRNAs do not have the prerequisite anchoring for the standardized guide segmentation, they would recognize targets differently from miRNAs and siRNAs. Cold Spring Harbor Laboratory 2023-10-28 /pmc/articles/PMC10634876/ /pubmed/37961191 http://dx.doi.org/10.1101/2023.10.27.564437 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Sim, GeunYoung
Kehling, Audrey C.
Park, Mi Seul
Divoky, Cameron
Zhang, Huaqun
Malhotra, Nipun
Secor, Jackson
Nakanishi, Kotaro
Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs
title Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs
title_full Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs
title_fullStr Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs
title_full_unstemmed Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs
title_short Determining the defining lengths between mature microRNAs/small interfering RNAs and tinyRNAs
title_sort determining the defining lengths between mature micrornas/small interfering rnas and tinyrnas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634876/
https://www.ncbi.nlm.nih.gov/pubmed/37961191
http://dx.doi.org/10.1101/2023.10.27.564437
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