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Integrative Analysis from the Epigenome to Translatome Uncovers Patterns of Dominant Nuclear Regulation during Transient Stress
Gene regulation is a dynamic process involving changes ranging from the remodeling of chromatin to preferential translation. To understand integrated nuclear and cytoplasmic gene regulatory dynamics, we performed a survey spanning the epigenome to translatome of Arabidopsis (Arabidopsis thaliana) se...
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Published in: | The Plant cell 2019-11, Vol.31 (11), p.2573-2595 |
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description | Gene regulation is a dynamic process involving changes ranging from the remodeling of chromatin to preferential translation. To understand integrated nuclear and cytoplasmic gene regulatory dynamics, we performed a survey spanning the epigenome to translatome of Arabidopsis (Arabidopsis thaliana) seedlings in response to hypoxia and reoxygenation. This included chromatin assays (examining histones, accessibility, RNA polymerase II [RNAPII], and transcription factor binding) and three RNA assays (nuclear, polyadenylated, and ribosome-associated). Dynamic patterns of nuclear regulation distinguished stress-induced and growth-associated mRNAs. The rapid upregulation of hypoxia-responsive gene transcripts and their preferential translation were generally accompanied by increased chromatin accessibility, RNAPII engagement, and reduced Histone 2A.Z association. Hypoxia promoted a progressive upregulation of heat stress transcripts, as evidenced by RNAPII binding and increased nuclear RNA, with polyadenylated RNA levels only elevated after prolonged stress or reoxygenation. Promoters of rapidly versus progressively upregulated genes were enriched for cis-elements of ethylene-responsive and heat shock factor transcription factors, respectively. Genes associated with growth, including many encoding cytosolic ribosomal proteins, underwent distinct histone modifications, yet retained RNAPII engagement and accumulated nuclear transcripts during the stress. Upon reaeration, progressively upregulated and growth-associated gene transcripts were rapidly mobilized to ribosomes. Thus, multilevel nuclear regulation of nucleosomes, transcript synthesis, accumulation, and translation tailor transient stress responses. |
doi_str_mv | 10.1105/tpc.19.00463 |
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To understand integrated nuclear and cytoplasmic gene regulatory dynamics, we performed a survey spanning the epigenome to translatome of Arabidopsis (Arabidopsis thaliana) seedlings in response to hypoxia and reoxygenation. This included chromatin assays (examining histones, accessibility, RNA polymerase II [RNAPII], and transcription factor binding) and three RNA assays (nuclear, polyadenylated, and ribosome-associated). Dynamic patterns of nuclear regulation distinguished stress-induced and growth-associated mRNAs. The rapid upregulation of hypoxia-responsive gene transcripts and their preferential translation were generally accompanied by increased chromatin accessibility, RNAPII engagement, and reduced Histone 2A.Z association. Hypoxia promoted a progressive upregulation of heat stress transcripts, as evidenced by RNAPII binding and increased nuclear RNA, with polyadenylated RNA levels only elevated after prolonged stress or reoxygenation. Promoters of rapidly versus progressively upregulated genes were enriched for cis-elements of ethylene-responsive and heat shock factor transcription factors, respectively. Genes associated with growth, including many encoding cytosolic ribosomal proteins, underwent distinct histone modifications, yet retained RNAPII engagement and accumulated nuclear transcripts during the stress. Upon reaeration, progressively upregulated and growth-associated gene transcripts were rapidly mobilized to ribosomes. Thus, multilevel nuclear regulation of nucleosomes, transcript synthesis, accumulation, and translation tailor transient stress responses.</description><identifier>ISSN: 1040-4651</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1105/tpc.19.00463</identifier><identifier>PMID: 31519798</identifier><language>eng</language><publisher>England: American Society of Plant Biologists (ASPB)</publisher><subject>Arabidopsis - genetics ; Arabidopsis - growth & development ; Arabidopsis Proteins - genetics ; Arabidopsis Proteins - metabolism ; Chromatin - metabolism ; Epigenome ; Gene Expression Regulation, Plant - genetics ; Gene Expression Regulation, Plant - physiology ; Genes, Plant - genetics ; Histones - metabolism ; Hot Temperature ; Large-Scale Biology ; LARGE-SCALE BIOLOGY ARTICLE ; Nucleosomes - metabolism ; Oxidative Stress ; Promoter Regions, Genetic ; Ribosomal Proteins ; Ribosomes ; RNA Polymerase II ; RNA, Messenger - metabolism ; Seedlings - genetics ; Stress, Physiological - genetics ; Stress, Physiological - physiology ; Transcription Factors ; Transcriptional Activation</subject><ispartof>The Plant cell, 2019-11, Vol.31 (11), p.2573-2595</ispartof><rights>2019 ASPB</rights><rights>2019 American Society of Plant Biologists. All rights reserved.</rights><rights>2019 American Society of Plant Biologists. All rights reserved. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-eff639141c065ae7de5651ee18cd9e2a49ab7eb71db17db87fd11eef7d6f77633</citedby><orcidid>0000-0002-8568-7125 ; 0000-0002-8352-8956</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31519798$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Travis A.</creatorcontrib><creatorcontrib>Bailey-Serres, Julia</creatorcontrib><title>Integrative Analysis from the Epigenome to Translatome Uncovers Patterns of Dominant Nuclear Regulation during Transient Stress</title><title>The Plant cell</title><addtitle>Plant Cell</addtitle><description>Gene regulation is a dynamic process involving changes ranging from the remodeling of chromatin to preferential translation. To understand integrated nuclear and cytoplasmic gene regulatory dynamics, we performed a survey spanning the epigenome to translatome of Arabidopsis (Arabidopsis thaliana) seedlings in response to hypoxia and reoxygenation. This included chromatin assays (examining histones, accessibility, RNA polymerase II [RNAPII], and transcription factor binding) and three RNA assays (nuclear, polyadenylated, and ribosome-associated). Dynamic patterns of nuclear regulation distinguished stress-induced and growth-associated mRNAs. The rapid upregulation of hypoxia-responsive gene transcripts and their preferential translation were generally accompanied by increased chromatin accessibility, RNAPII engagement, and reduced Histone 2A.Z association. Hypoxia promoted a progressive upregulation of heat stress transcripts, as evidenced by RNAPII binding and increased nuclear RNA, with polyadenylated RNA levels only elevated after prolonged stress or reoxygenation. Promoters of rapidly versus progressively upregulated genes were enriched for cis-elements of ethylene-responsive and heat shock factor transcription factors, respectively. Genes associated with growth, including many encoding cytosolic ribosomal proteins, underwent distinct histone modifications, yet retained RNAPII engagement and accumulated nuclear transcripts during the stress. Upon reaeration, progressively upregulated and growth-associated gene transcripts were rapidly mobilized to ribosomes. Thus, multilevel nuclear regulation of nucleosomes, transcript synthesis, accumulation, and translation tailor transient stress responses.</description><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - growth & development</subject><subject>Arabidopsis Proteins - genetics</subject><subject>Arabidopsis Proteins - metabolism</subject><subject>Chromatin - metabolism</subject><subject>Epigenome</subject><subject>Gene Expression Regulation, Plant - genetics</subject><subject>Gene Expression Regulation, Plant - physiology</subject><subject>Genes, Plant - genetics</subject><subject>Histones - metabolism</subject><subject>Hot Temperature</subject><subject>Large-Scale Biology</subject><subject>LARGE-SCALE BIOLOGY ARTICLE</subject><subject>Nucleosomes - metabolism</subject><subject>Oxidative Stress</subject><subject>Promoter Regions, Genetic</subject><subject>Ribosomal Proteins</subject><subject>Ribosomes</subject><subject>RNA Polymerase II</subject><subject>RNA, Messenger - metabolism</subject><subject>Seedlings - genetics</subject><subject>Stress, Physiological - genetics</subject><subject>Stress, Physiological - physiology</subject><subject>Transcription Factors</subject><subject>Transcriptional Activation</subject><issn>1040-4651</issn><issn>1532-298X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpVkc9vFCEYhonR2Np686rh6MFZ-eYXw8WkqVWbNLXRNvFGGOZjSjMDW2A26cl_Xdatm3oC8j68fOQh5A2wFQBrPqa1XoFYMVa31TNyCE1VFqXofj3Pe1azom4bOCCvYrxjjAEH8ZIcVNCA4KI7JL_PXcIxqGQ3SE-cmh6ijdQEP9N0i_RsbUd0fkaaPL0OysVJpe3xxmm_wRDplUoJg4vUG_rZz9Ypl-jloidUgf7AcckXrHd0WIJ1467DYmZ-poAxHpMXRk0RXz-uR-Tmy9n16bfi4vvX89OTi0LXvEwFGtNWAmrQrG0U8gGb_C1E6PQgsFS1UD3HnsPQAx_6jpsBcmz40BrO26o6Ip92veuln3HQeYKgJrkOdlbhQXpl5f-Js7dy9BvZdh1AyXLB-8eC4O8XjEnONmqcJuXQL1GWpWAiS2Bb9MMO1cHHGNDsnwEmt85kdiZByL_OMv7u6Wh7-J-kDLzdAXcx-bDPy7Zroam76g-boqEM</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Lee, Travis A.</creator><creator>Bailey-Serres, Julia</creator><general>American Society of Plant Biologists (ASPB)</general><general>American Society of Plant Biologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8568-7125</orcidid><orcidid>https://orcid.org/0000-0002-8352-8956</orcidid></search><sort><creationdate>20191101</creationdate><title>Integrative Analysis from the Epigenome to Translatome Uncovers Patterns of Dominant Nuclear Regulation during Transient Stress</title><author>Lee, Travis A. ; Bailey-Serres, Julia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-eff639141c065ae7de5651ee18cd9e2a49ab7eb71db17db87fd11eef7d6f77633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - growth & development</topic><topic>Arabidopsis Proteins - genetics</topic><topic>Arabidopsis Proteins - metabolism</topic><topic>Chromatin - metabolism</topic><topic>Epigenome</topic><topic>Gene Expression Regulation, Plant - genetics</topic><topic>Gene Expression Regulation, Plant - physiology</topic><topic>Genes, Plant - genetics</topic><topic>Histones - metabolism</topic><topic>Hot Temperature</topic><topic>Large-Scale Biology</topic><topic>LARGE-SCALE BIOLOGY ARTICLE</topic><topic>Nucleosomes - metabolism</topic><topic>Oxidative Stress</topic><topic>Promoter Regions, Genetic</topic><topic>Ribosomal Proteins</topic><topic>Ribosomes</topic><topic>RNA Polymerase II</topic><topic>RNA, Messenger - metabolism</topic><topic>Seedlings - genetics</topic><topic>Stress, Physiological - genetics</topic><topic>Stress, Physiological - physiology</topic><topic>Transcription Factors</topic><topic>Transcriptional Activation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Travis A.</creatorcontrib><creatorcontrib>Bailey-Serres, Julia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Plant cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Travis A.</au><au>Bailey-Serres, Julia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Integrative Analysis from the Epigenome to Translatome Uncovers Patterns of Dominant Nuclear Regulation during Transient Stress</atitle><jtitle>The Plant cell</jtitle><addtitle>Plant Cell</addtitle><date>2019-11-01</date><risdate>2019</risdate><volume>31</volume><issue>11</issue><spage>2573</spage><epage>2595</epage><pages>2573-2595</pages><issn>1040-4651</issn><eissn>1532-298X</eissn><abstract>Gene regulation is a dynamic process involving changes ranging from the remodeling of chromatin to preferential translation. To understand integrated nuclear and cytoplasmic gene regulatory dynamics, we performed a survey spanning the epigenome to translatome of Arabidopsis (Arabidopsis thaliana) seedlings in response to hypoxia and reoxygenation. This included chromatin assays (examining histones, accessibility, RNA polymerase II [RNAPII], and transcription factor binding) and three RNA assays (nuclear, polyadenylated, and ribosome-associated). Dynamic patterns of nuclear regulation distinguished stress-induced and growth-associated mRNAs. The rapid upregulation of hypoxia-responsive gene transcripts and their preferential translation were generally accompanied by increased chromatin accessibility, RNAPII engagement, and reduced Histone 2A.Z association. Hypoxia promoted a progressive upregulation of heat stress transcripts, as evidenced by RNAPII binding and increased nuclear RNA, with polyadenylated RNA levels only elevated after prolonged stress or reoxygenation. Promoters of rapidly versus progressively upregulated genes were enriched for cis-elements of ethylene-responsive and heat shock factor transcription factors, respectively. Genes associated with growth, including many encoding cytosolic ribosomal proteins, underwent distinct histone modifications, yet retained RNAPII engagement and accumulated nuclear transcripts during the stress. Upon reaeration, progressively upregulated and growth-associated gene transcripts were rapidly mobilized to ribosomes. Thus, multilevel nuclear regulation of nucleosomes, transcript synthesis, accumulation, and translation tailor transient stress responses.</abstract><cop>England</cop><pub>American Society of Plant Biologists (ASPB)</pub><pmid>31519798</pmid><doi>10.1105/tpc.19.00463</doi><tpages>23</tpages><orcidid>https://orcid.org/0000-0002-8568-7125</orcidid><orcidid>https://orcid.org/0000-0002-8352-8956</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Arabidopsis - genetics Arabidopsis - growth & development Arabidopsis Proteins - genetics Arabidopsis Proteins - metabolism Chromatin - metabolism Epigenome Gene Expression Regulation, Plant - genetics Gene Expression Regulation, Plant - physiology Genes, Plant - genetics Histones - metabolism Hot Temperature Large-Scale Biology LARGE-SCALE BIOLOGY ARTICLE Nucleosomes - metabolism Oxidative Stress Promoter Regions, Genetic Ribosomal Proteins Ribosomes RNA Polymerase II RNA, Messenger - metabolism Seedlings - genetics Stress, Physiological - genetics Stress, Physiological - physiology Transcription Factors Transcriptional Activation |
title | Integrative Analysis from the Epigenome to Translatome Uncovers Patterns of Dominant Nuclear Regulation during Transient Stress |
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