A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish

The RNAi pathway provides both innate immunity and efficient gene-knockdown tools in many eukaryotic species, but curiously not in zebrafish. We discovered that RNAi is less effective in zebrafish at least partly because Argonaute2-catalyzed mRNA slicing is impaired. This defect is due to two mutati...

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Main Authors: Chen, Grace, Bartel, David, Sive, Hazel L.
其他作者: Massachusetts Institute of Technology. Department of Biology
格式: 文件
出版: Elsevier BV 2019
在线阅读:http://hdl.handle.net/1721.1/120144
https://orcid.org/0000-0001-9051-1696
https://orcid.org/0000-0002-4890-424X
https://orcid.org/0000-0002-3872-2856
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author Chen, Grace
Bartel, David
Sive, Hazel L.
author2 Massachusetts Institute of Technology. Department of Biology
author_facet Massachusetts Institute of Technology. Department of Biology
Chen, Grace
Bartel, David
Sive, Hazel L.
author_sort Chen, Grace
collection MIT
description The RNAi pathway provides both innate immunity and efficient gene-knockdown tools in many eukaryotic species, but curiously not in zebrafish. We discovered that RNAi is less effective in zebrafish at least partly because Argonaute2-catalyzed mRNA slicing is impaired. This defect is due to two mutations that arose in an ancestor of most teleost fish, implying that most fish lack effective RNAi. Despite lacking efficient slicing activity, these fish have retained the ability to produce miR-451, a microRNA generated by a cleavage reaction analogous to slicing. This ability is due to a G–G mismatch within the fish miR-451 precursor, which substantially enhances its cleavage. An analogous G–G mismatch (or sometimes also a G–A mismatch) enhances target slicing, despite disrupting seed pairing important for target binding. These results provide a strategy for restoring RNAi to zebrafish and reveal unanticipated opposing effects of a seed mismatch with implications for mechanism and guide-RNA design. Chen et al. discover two substitutions that restore normal slicing activity to zebrafish Argonaute2 and a mismatch involving guide-RNA position 6 that further enhances this activity. These findings suggest a strategy for enabling efficient RNAi in zebrafish and show that some seed mismatches have opposing effects on binding and slicing. Keywords: Argonaute; AGO2; RISC; RNAi; in vitro slicing; miRNA; miR-451 processing; siRNA design; kinetic analysis
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spelling mit-1721.1/1201442022-09-26T15:07:20Z A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish Chen, Grace Bartel, David Sive, Hazel L. Massachusetts Institute of Technology. Department of Biology Chen, Grace Sive, Hazel L Bartel, David The RNAi pathway provides both innate immunity and efficient gene-knockdown tools in many eukaryotic species, but curiously not in zebrafish. We discovered that RNAi is less effective in zebrafish at least partly because Argonaute2-catalyzed mRNA slicing is impaired. This defect is due to two mutations that arose in an ancestor of most teleost fish, implying that most fish lack effective RNAi. Despite lacking efficient slicing activity, these fish have retained the ability to produce miR-451, a microRNA generated by a cleavage reaction analogous to slicing. This ability is due to a G–G mismatch within the fish miR-451 precursor, which substantially enhances its cleavage. An analogous G–G mismatch (or sometimes also a G–A mismatch) enhances target slicing, despite disrupting seed pairing important for target binding. These results provide a strategy for restoring RNAi to zebrafish and reveal unanticipated opposing effects of a seed mismatch with implications for mechanism and guide-RNA design. Chen et al. discover two substitutions that restore normal slicing activity to zebrafish Argonaute2 and a mismatch involving guide-RNA position 6 that further enhances this activity. These findings suggest a strategy for enabling efficient RNAi in zebrafish and show that some seed mismatches have opposing effects on binding and slicing. Keywords: Argonaute; AGO2; RISC; RNAi; in vitro slicing; miRNA; miR-451 processing; siRNA design; kinetic analysis National Institutes of Health (U.S.) (Grant GM061835) National Institutes of Health (U.S.) (Grant GM118135) 2019-01-29T20:12:39Z 2019-01-29T20:12:39Z 2017-12 2017-10 2019-01-18T13:46:57Z Article http://purl.org/eprint/type/JournalArticle 1097-2765 1097-4164 http://hdl.handle.net/1721.1/120144 Chen, Grace R. et al. “A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish.” Molecular Cell 68, 6 (December 2017): 1095–1107 © 2017 Elsevier https://orcid.org/0000-0001-9051-1696 https://orcid.org/0000-0002-4890-424X https://orcid.org/0000-0002-3872-2856 http://dx.doi.org/10.1016/J.MOLCEL.2017.11.032 Molecular Cell Creative Commons Attribution-NonCommercial-NoDerivs License http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier BV PMC
spellingShingle Chen, Grace
Bartel, David
Sive, Hazel L.
A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish
title A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish
title_full A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish
title_fullStr A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish
title_full_unstemmed A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish
title_short A Seed Mismatch Enhances Argonaute2-Catalyzed Cleavage and Partially Rescues Severely Impaired Cleavage Found in Fish
title_sort seed mismatch enhances argonaute2 catalyzed cleavage and partially rescues severely impaired cleavage found in fish
url http://hdl.handle.net/1721.1/120144
https://orcid.org/0000-0001-9051-1696
https://orcid.org/0000-0002-4890-424X
https://orcid.org/0000-0002-3872-2856
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