N 6 -methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis
After transcription, a messenger RNA (mRNA) is further post-transcriptionally regulated by several features including RNA secondary structure and covalent RNA modifications (specifically N -methyladenosine, m A). Both RNA secondary structure and m A have been demonstrated to regulate mRNA stability...
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creator | Kramer, Marianne C Janssen, Kevin A Palos, Kyle Nelson, Andrew D L Vandivier, Lee E Garcia, Benjamin A Lyons, Eric Beilstein, Mark A Gregory, Brian D |
description | After transcription, a messenger RNA (mRNA) is further post-transcriptionally regulated by several features including RNA secondary structure and covalent RNA modifications (specifically N
-methyladenosine, m
A). Both RNA secondary structure and m
A have been demonstrated to regulate mRNA stability and translation and have been independently linked to plant responses to soil salinity levels. However, the effect of m
A on regulating RNA secondary structure and the combinatorial interplay between these two RNA features during salt stress response has yet to be studied. Here, we globally identify RNA-protein interactions and RNA secondary structure during systemic salt stress. This analysis reveals that RNA secondary structure changes significantly during salt stress, and that it is independent of global changes in RNA-protein interactions. Conversely, we find that m
A is anti-correlated with RNA secondary structure in a condition-dependent manner, with salt-specific m
A correlated with a decrease in mRNA secondary structure during salt stress. Taken together, we suggest that salt-specific m
A deposition and the associated loss of RNA secondary structure results in increases in mRNA stability for transcripts encoding abiotic stress response proteins and ultimately increases in protein levels from these stabilized transcripts. In total, our comprehensive analyses reveal important post-transcriptional regulatory mechanisms involved in plant long-term salt stress response and adaptation. |
doi_str_mv | 10.1002/pld3.239 |
format | Article |
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-methyladenosine, m
A). Both RNA secondary structure and m
A have been demonstrated to regulate mRNA stability and translation and have been independently linked to plant responses to soil salinity levels. However, the effect of m
A on regulating RNA secondary structure and the combinatorial interplay between these two RNA features during salt stress response has yet to be studied. Here, we globally identify RNA-protein interactions and RNA secondary structure during systemic salt stress. This analysis reveals that RNA secondary structure changes significantly during salt stress, and that it is independent of global changes in RNA-protein interactions. Conversely, we find that m
A is anti-correlated with RNA secondary structure in a condition-dependent manner, with salt-specific m
A correlated with a decrease in mRNA secondary structure during salt stress. Taken together, we suggest that salt-specific m
A deposition and the associated loss of RNA secondary structure results in increases in mRNA stability for transcripts encoding abiotic stress response proteins and ultimately increases in protein levels from these stabilized transcripts. In total, our comprehensive analyses reveal important post-transcriptional regulatory mechanisms involved in plant long-term salt stress response and adaptation.</description><identifier>ISSN: 2475-4455</identifier><identifier>EISSN: 2475-4455</identifier><identifier>DOI: 10.1002/pld3.239</identifier><identifier>PMID: 32724893</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>Abiotic stress ; Binding sites ; Mass spectrometry ; mRNA stability ; N6-methyladenosine ; Protein interaction ; Protein structure ; Proteins ; Salinity ; Scientific imaging ; Secondary structure ; Soil salinity ; Transcription</subject><ispartof>Plant direct, 2020-07, Vol.4 (7), p.e00239</ispartof><rights>2020 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd.</rights><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1233-d4bcae257747d78ace248bbb53b7827aeaed9e80453ed996053725c4fd7b62a03</citedby><cites>FETCH-LOGICAL-c1233-d4bcae257747d78ace248bbb53b7827aeaed9e80453ed996053725c4fd7b62a03</cites><orcidid>0000-0001-9896-1739 ; 0000-0001-7532-0138 ; 0000-0002-6980-9575 ; 0000-0002-5699-8354 ; 0000-0001-7788-5888 ; 0000-0002-2306-1207 ; 0000-0002-3392-1389</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32724893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kramer, Marianne C</creatorcontrib><creatorcontrib>Janssen, Kevin A</creatorcontrib><creatorcontrib>Palos, Kyle</creatorcontrib><creatorcontrib>Nelson, Andrew D L</creatorcontrib><creatorcontrib>Vandivier, Lee E</creatorcontrib><creatorcontrib>Garcia, Benjamin A</creatorcontrib><creatorcontrib>Lyons, Eric</creatorcontrib><creatorcontrib>Beilstein, Mark A</creatorcontrib><creatorcontrib>Gregory, Brian D</creatorcontrib><title>N 6 -methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis</title><title>Plant direct</title><addtitle>Plant Direct</addtitle><description>After transcription, a messenger RNA (mRNA) is further post-transcriptionally regulated by several features including RNA secondary structure and covalent RNA modifications (specifically N
-methyladenosine, m
A). Both RNA secondary structure and m
A have been demonstrated to regulate mRNA stability and translation and have been independently linked to plant responses to soil salinity levels. However, the effect of m
A on regulating RNA secondary structure and the combinatorial interplay between these two RNA features during salt stress response has yet to be studied. Here, we globally identify RNA-protein interactions and RNA secondary structure during systemic salt stress. This analysis reveals that RNA secondary structure changes significantly during salt stress, and that it is independent of global changes in RNA-protein interactions. Conversely, we find that m
A is anti-correlated with RNA secondary structure in a condition-dependent manner, with salt-specific m
A correlated with a decrease in mRNA secondary structure during salt stress. Taken together, we suggest that salt-specific m
A deposition and the associated loss of RNA secondary structure results in increases in mRNA stability for transcripts encoding abiotic stress response proteins and ultimately increases in protein levels from these stabilized transcripts. In total, our comprehensive analyses reveal important post-transcriptional regulatory mechanisms involved in plant long-term salt stress response and adaptation.</description><subject>Abiotic stress</subject><subject>Binding sites</subject><subject>Mass spectrometry</subject><subject>mRNA stability</subject><subject>N6-methyladenosine</subject><subject>Protein interaction</subject><subject>Protein structure</subject><subject>Proteins</subject><subject>Salinity</subject><subject>Scientific imaging</subject><subject>Secondary structure</subject><subject>Soil salinity</subject><subject>Transcription</subject><issn>2475-4455</issn><issn>2475-4455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpNkMtKJTEQhsPgMMpR8Akk4MZNO-lcOt3Lg3gDcUDGdZNL9Rjpk25T6cV5CN_ZnPGCqyqo769KPkKOa3ZeM8Z_z6MX51x0P8gBl1pVUiq1963fJ0eIz6ygtW5Yq36RfcE1l20nDsjrPW1otYH8tB2NhzhhiEBN9PThfk0R3BS9SVuKOS0uL6nMhgFcpjmZiC6FOZeZsWEMefs_N6cpQ4jU2KVEowPqlxTiP4pbzLAJjqIZd6EEiLSA61Tifpox4CH5OZgR4eijrsjj1eXfi5vq7s_17cX6rnI1F6Ly0joDXGkttdetcVB-Y61VwuqWawMGfActk0qUpmuYEporJwevbcMNEyty-r63PPZlAcz987SkWE72XPJOdW0j6kKdvVMuTYgJhn5OYVNs9DXrd-r7nfq-qC_oycfCxW7Af4GfosUb67GBEw</recordid><startdate>202007</startdate><enddate>202007</enddate><creator>Kramer, Marianne C</creator><creator>Janssen, Kevin A</creator><creator>Palos, Kyle</creator><creator>Nelson, Andrew D L</creator><creator>Vandivier, Lee E</creator><creator>Garcia, Benjamin A</creator><creator>Lyons, Eric</creator><creator>Beilstein, Mark A</creator><creator>Gregory, Brian D</creator><general>John Wiley & Sons, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0001-9896-1739</orcidid><orcidid>https://orcid.org/0000-0001-7532-0138</orcidid><orcidid>https://orcid.org/0000-0002-6980-9575</orcidid><orcidid>https://orcid.org/0000-0002-5699-8354</orcidid><orcidid>https://orcid.org/0000-0001-7788-5888</orcidid><orcidid>https://orcid.org/0000-0002-2306-1207</orcidid><orcidid>https://orcid.org/0000-0002-3392-1389</orcidid></search><sort><creationdate>202007</creationdate><title>N 6 -methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis</title><author>Kramer, Marianne C ; Janssen, Kevin A ; Palos, Kyle ; Nelson, Andrew D L ; Vandivier, Lee E ; Garcia, Benjamin A ; Lyons, Eric ; Beilstein, Mark A ; Gregory, Brian D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1233-d4bcae257747d78ace248bbb53b7827aeaed9e80453ed996053725c4fd7b62a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Abiotic stress</topic><topic>Binding sites</topic><topic>Mass spectrometry</topic><topic>mRNA stability</topic><topic>N6-methyladenosine</topic><topic>Protein interaction</topic><topic>Protein structure</topic><topic>Proteins</topic><topic>Salinity</topic><topic>Scientific imaging</topic><topic>Secondary structure</topic><topic>Soil salinity</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kramer, Marianne C</creatorcontrib><creatorcontrib>Janssen, Kevin A</creatorcontrib><creatorcontrib>Palos, Kyle</creatorcontrib><creatorcontrib>Nelson, Andrew D L</creatorcontrib><creatorcontrib>Vandivier, Lee E</creatorcontrib><creatorcontrib>Garcia, Benjamin A</creatorcontrib><creatorcontrib>Lyons, Eric</creatorcontrib><creatorcontrib>Beilstein, Mark A</creatorcontrib><creatorcontrib>Gregory, Brian D</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Plant direct</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kramer, Marianne C</au><au>Janssen, Kevin A</au><au>Palos, Kyle</au><au>Nelson, Andrew D L</au><au>Vandivier, Lee E</au><au>Garcia, Benjamin A</au><au>Lyons, Eric</au><au>Beilstein, Mark A</au><au>Gregory, Brian D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N 6 -methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis</atitle><jtitle>Plant direct</jtitle><addtitle>Plant Direct</addtitle><date>2020-07</date><risdate>2020</risdate><volume>4</volume><issue>7</issue><spage>e00239</spage><pages>e00239-</pages><issn>2475-4455</issn><eissn>2475-4455</eissn><abstract>After transcription, a messenger RNA (mRNA) is further post-transcriptionally regulated by several features including RNA secondary structure and covalent RNA modifications (specifically N
-methyladenosine, m
A). Both RNA secondary structure and m
A have been demonstrated to regulate mRNA stability and translation and have been independently linked to plant responses to soil salinity levels. However, the effect of m
A on regulating RNA secondary structure and the combinatorial interplay between these two RNA features during salt stress response has yet to be studied. Here, we globally identify RNA-protein interactions and RNA secondary structure during systemic salt stress. This analysis reveals that RNA secondary structure changes significantly during salt stress, and that it is independent of global changes in RNA-protein interactions. Conversely, we find that m
A is anti-correlated with RNA secondary structure in a condition-dependent manner, with salt-specific m
A correlated with a decrease in mRNA secondary structure during salt stress. Taken together, we suggest that salt-specific m
A deposition and the associated loss of RNA secondary structure results in increases in mRNA stability for transcripts encoding abiotic stress response proteins and ultimately increases in protein levels from these stabilized transcripts. In total, our comprehensive analyses reveal important post-transcriptional regulatory mechanisms involved in plant long-term salt stress response and adaptation.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>32724893</pmid><doi>10.1002/pld3.239</doi><orcidid>https://orcid.org/0000-0001-9896-1739</orcidid><orcidid>https://orcid.org/0000-0001-7532-0138</orcidid><orcidid>https://orcid.org/0000-0002-6980-9575</orcidid><orcidid>https://orcid.org/0000-0002-5699-8354</orcidid><orcidid>https://orcid.org/0000-0001-7788-5888</orcidid><orcidid>https://orcid.org/0000-0002-2306-1207</orcidid><orcidid>https://orcid.org/0000-0002-3392-1389</orcidid><oa>free_for_read</oa></addata></record> |
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source | Wiley Journals; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Wiley-Blackwell Open Access Titles; PubMed Central |
subjects | Abiotic stress Binding sites Mass spectrometry mRNA stability N6-methyladenosine Protein interaction Protein structure Proteins Salinity Scientific imaging Secondary structure Soil salinity Transcription |
title | N 6 -methyladenosine and RNA secondary structure affect transcript stability and protein abundance during systemic salt stress in Arabidopsis |
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