Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets

MicroRNAs (miRNAs) direct post-transcriptional regulation of human genes by guiding Argonaute proteins to complementary sites in messenger RNAs (mRNAs) targeted for repression. An enigmatic feature of many conserved mammalian miRNA target sites is that an adenosine (A) nucleotide opposite miRNA nucl...

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Main Authors: Nicole T Schirle, Jessica Sheu-Gruttadauria, Stanley D Chandradoss, Chirlmin Joo, Ian J MacRae
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2015-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/07646
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spelling doaj-b488e6ba7de44b14ac4ed2010e91cec22021-05-05T00:01:02ZengeLife Sciences Publications LtdeLife2050-084X2015-09-01410.7554/eLife.07646Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targetsNicole T Schirle0Jessica Sheu-Gruttadauria1Stanley D Chandradoss2Chirlmin Joo3Ian J MacRae4Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, United StatesDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, United StatesKavli Institute of NanoScience, Department of BioNanoScience, Delft University of Technology, Delft, NetherlandsKavli Institute of NanoScience, Department of BioNanoScience, Delft University of Technology, Delft, NetherlandsDepartment of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, United StatesMicroRNAs (miRNAs) direct post-transcriptional regulation of human genes by guiding Argonaute proteins to complementary sites in messenger RNAs (mRNAs) targeted for repression. An enigmatic feature of many conserved mammalian miRNA target sites is that an adenosine (A) nucleotide opposite miRNA nucleotide-1 confers enhanced target repression independently of base pairing potential to the miRNA. In this study, we show that human Argonaute2 (Ago2) possesses a solvated surface pocket that specifically binds adenine nucleobases in the 1 position (t1) of target RNAs. t1A nucleotides are recognized indirectly through a hydrogen-bonding network of water molecules that preferentially interacts with the N6 amine on adenine. t1A nucleotides are not utilized during the initial binding of Ago2 to its target, but instead function by increasing the dwell time on target RNA. We also show that N6 adenosine methylation blocks t1A recognition, revealing a possible mechanism for modulation of miRNA target site potency.https://elifesciences.org/articles/07646microRNAArgonauteRNA silencing
collection DOAJ
language English
format Article
sources DOAJ
author Nicole T Schirle
Jessica Sheu-Gruttadauria
Stanley D Chandradoss
Chirlmin Joo
Ian J MacRae
spellingShingle Nicole T Schirle
Jessica Sheu-Gruttadauria
Stanley D Chandradoss
Chirlmin Joo
Ian J MacRae
Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets
eLife
microRNA
Argonaute
RNA silencing
author_facet Nicole T Schirle
Jessica Sheu-Gruttadauria
Stanley D Chandradoss
Chirlmin Joo
Ian J MacRae
author_sort Nicole T Schirle
title Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets
title_short Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets
title_full Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets
title_fullStr Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets
title_full_unstemmed Water-mediated recognition of t1-adenosine anchors Argonaute2 to microRNA targets
title_sort water-mediated recognition of t1-adenosine anchors argonaute2 to microrna targets
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2015-09-01
description MicroRNAs (miRNAs) direct post-transcriptional regulation of human genes by guiding Argonaute proteins to complementary sites in messenger RNAs (mRNAs) targeted for repression. An enigmatic feature of many conserved mammalian miRNA target sites is that an adenosine (A) nucleotide opposite miRNA nucleotide-1 confers enhanced target repression independently of base pairing potential to the miRNA. In this study, we show that human Argonaute2 (Ago2) possesses a solvated surface pocket that specifically binds adenine nucleobases in the 1 position (t1) of target RNAs. t1A nucleotides are recognized indirectly through a hydrogen-bonding network of water molecules that preferentially interacts with the N6 amine on adenine. t1A nucleotides are not utilized during the initial binding of Ago2 to its target, but instead function by increasing the dwell time on target RNA. We also show that N6 adenosine methylation blocks t1A recognition, revealing a possible mechanism for modulation of miRNA target site potency.
topic microRNA
Argonaute
RNA silencing
url https://elifesciences.org/articles/07646
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