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Anatomy of four human Argonaute proteins

MicroRNAs (miRNAs) bind to complementary target RNAs and regulate their gene expression post-transcriptionally. These non-coding regulatory RNAs become functional after loading into Argonaute (AGO) proteins to form the effector complexes. Humans have four AGO proteins, AGO1, AGO2, AGO3 and AGO4, whi...

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Autor principal: Nakanishi, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262622/
https://www.ncbi.nlm.nih.gov/pubmed/35736234
http://dx.doi.org/10.1093/nar/gkac519
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author Nakanishi, Kotaro
author_facet Nakanishi, Kotaro
author_sort Nakanishi, Kotaro
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description MicroRNAs (miRNAs) bind to complementary target RNAs and regulate their gene expression post-transcriptionally. These non-coding regulatory RNAs become functional after loading into Argonaute (AGO) proteins to form the effector complexes. Humans have four AGO proteins, AGO1, AGO2, AGO3 and AGO4, which share a high sequence identity. Since most miRNAs are found across the four AGOs, it has been thought that they work redundantly, and AGO2 has been heavily studied as the exemplified human paralog. Nevertheless, an increasing number of studies have found that the other paralogs play unique roles in various biological processes and diseases. In the last decade, the structural study of the four AGOs has provided the field with solid structural bases. This review exploits the completed structural catalog to describe common features and differences in target specificity across the four AGOs.
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spelling pubmed-92626222022-07-08 Anatomy of four human Argonaute proteins Nakanishi, Kotaro Nucleic Acids Res Critical Reviews and Perspectives MicroRNAs (miRNAs) bind to complementary target RNAs and regulate their gene expression post-transcriptionally. These non-coding regulatory RNAs become functional after loading into Argonaute (AGO) proteins to form the effector complexes. Humans have four AGO proteins, AGO1, AGO2, AGO3 and AGO4, which share a high sequence identity. Since most miRNAs are found across the four AGOs, it has been thought that they work redundantly, and AGO2 has been heavily studied as the exemplified human paralog. Nevertheless, an increasing number of studies have found that the other paralogs play unique roles in various biological processes and diseases. In the last decade, the structural study of the four AGOs has provided the field with solid structural bases. This review exploits the completed structural catalog to describe common features and differences in target specificity across the four AGOs. Oxford University Press 2022-06-23 /pmc/articles/PMC9262622/ /pubmed/35736234 http://dx.doi.org/10.1093/nar/gkac519 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Critical Reviews and Perspectives
Nakanishi, Kotaro
Anatomy of four human Argonaute proteins
title Anatomy of four human Argonaute proteins
title_full Anatomy of four human Argonaute proteins
title_fullStr Anatomy of four human Argonaute proteins
title_full_unstemmed Anatomy of four human Argonaute proteins
title_short Anatomy of four human Argonaute proteins
title_sort anatomy of four human argonaute proteins
topic Critical Reviews and Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262622/
https://www.ncbi.nlm.nih.gov/pubmed/35736234
http://dx.doi.org/10.1093/nar/gkac519
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