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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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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. |
format | Online Article Text |
id | pubmed-10634876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
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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