The transcriptional regulatory network mediated by banana (Musa acuminata) dehydration-responsive element binding (MaDREB) transcription factors in fruit ripening
Fruit ripening is a complex, genetically programmed process involving the action of critical transcription factors (TFs). Despite the established significance of dehydration-responsive element binding (DREB) TFs in plant abiotic stress responses, the involvement of DREBs in fruit ripening is yet to...
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Veröffentlicht in: | The New phytologist 2017-04, Vol.214 (2), p.762-781 |
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container_title | The New phytologist |
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creator | Kuang, Jian‐Fei Chen, Jian‐Ye Liu, Xun‐Cheng Han, Yan‐Chao Xiao, Yun‐Yi Shan, Wei Tang, Yang Wu, Ke‐Qiang He, Jun‐Xian Lu, Wang‐Jin |
description | Fruit ripening is a complex, genetically programmed process involving the action of critical transcription factors (TFs). Despite the established significance of dehydration-responsive element binding (DREB) TFs in plant abiotic stress responses, the involvement of DREBs in fruit ripening is yet to be determined.
Here, we identified four genes encoding ripening-regulated DREB TFs in banana (Musa acuminata), MaDREB1, MaDREB2, MaDREB3, and MaDREB4, and demonstrated that they play regulatory roles in fruit ripening.
We showed that MaDREB1–MaDREB4 are nucleus-localized, induced by ethylene and encompass transcriptional activation activities. We performed a genome-wide chromatin immunoprecipitation and high-throughput sequencing (ChIP-Seq) experiment for MaDREB2 and identified 697 genomic regions as potential targets of MaDREB2. MaDREB2 binds to hundreds of loci with diverse functions and its binding sites are distributed in the promoter regions proximal to the transcriptional start site (TSS). Most of the MaDREB2-binding targets contain the conserved (A/G)CC(G/C)AC motif and MaDREB2 appears to directly regulate the expression of a number of genes involved in fruit ripening. In combination with transcriptome profiling (RNA sequencing) data, our results indicate that MaDREB2 may serve as both transcriptional activator and repressor during banana fruit ripening.
In conclusion, our study suggests a hierarchical regulatory model of fruit ripening in banana and that the MaDREB TFs may act as transcriptional regulators in the regulatory network. |
doi_str_mv | 10.1111/nph.14389 |
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Here, we identified four genes encoding ripening-regulated DREB TFs in banana (Musa acuminata), MaDREB1, MaDREB2, MaDREB3, and MaDREB4, and demonstrated that they play regulatory roles in fruit ripening.
We showed that MaDREB1–MaDREB4 are nucleus-localized, induced by ethylene and encompass transcriptional activation activities. We performed a genome-wide chromatin immunoprecipitation and high-throughput sequencing (ChIP-Seq) experiment for MaDREB2 and identified 697 genomic regions as potential targets of MaDREB2. MaDREB2 binds to hundreds of loci with diverse functions and its binding sites are distributed in the promoter regions proximal to the transcriptional start site (TSS). Most of the MaDREB2-binding targets contain the conserved (A/G)CC(G/C)AC motif and MaDREB2 appears to directly regulate the expression of a number of genes involved in fruit ripening. In combination with transcriptome profiling (RNA sequencing) data, our results indicate that MaDREB2 may serve as both transcriptional activator and repressor during banana fruit ripening.
In conclusion, our study suggests a hierarchical regulatory model of fruit ripening in banana and that the MaDREB TFs may act as transcriptional regulators in the regulatory network.</description><identifier>ISSN: 0028-646X</identifier><identifier>EISSN: 1469-8137</identifier><identifier>DOI: 10.1111/nph.14389</identifier><identifier>PMID: 28044313</identifier><language>eng</language><publisher>England: New Phytologist Trust</publisher><subject>banana ; Base Sequence ; Binding sites ; Cell Wall - metabolism ; Chromatin ; chromatin immunoprecipitation coupled DNA sequencing (ChIP‐Seq) ; Dehydration ; dehydration‐responsive element binding (DREB) ; Down-Regulation - genetics ; Fruit - genetics ; Fruit - physiology ; fruit ripening ; Fruits ; Gene expression ; Gene Expression Regulation, Plant ; Gene Regulatory Networks - genetics ; Gene sequencing ; Genes ; Genes, Plant ; Genomes ; Identification ; Immunoprecipitation ; Musa ; Musa - genetics ; Musa - physiology ; Musa acuminata ; Next-generation sequencing ; Nuclei ; Nucleic acids ; Nucleotide Motifs - genetics ; Nucleus ; Plant Proteins - isolation & purification ; Plant Proteins - metabolism ; Promoter Regions, Genetic - genetics ; Promoters ; Protein Binding - genetics ; Regions ; Regulators ; Regulatory sequences ; Ribonucleic acid ; Ripening ; RNA ; RNA sequencing ; Sequencing ; Subcellular Fractions - metabolism ; Transcription ; Transcription activation ; Transcription factors ; Transcription Factors - isolation & purification ; Transcription Factors - metabolism ; Transcriptional Activation - genetics ; transcriptional regulation</subject><ispartof>The New phytologist, 2017-04, Vol.214 (2), p.762-781</ispartof><rights>2017 New Phytologist Trust</rights><rights>2017 The Authors. New Phytologist © 2017 New Phytologist Trust</rights><rights>2017 The Authors. New Phytologist © 2017 New Phytologist Trust.</rights><rights>Copyright © 2017 New Phytologist Trust</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4439-957093e3d27106f44daba89d3a3115343b1d769d147e3b1d239646274541754f3</citedby><cites>FETCH-LOGICAL-c4439-957093e3d27106f44daba89d3a3115343b1d769d147e3b1d239646274541754f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/90002002$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/90002002$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,1411,1427,27901,27902,45550,45551,46384,46808,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28044313$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuang, Jian‐Fei</creatorcontrib><creatorcontrib>Chen, Jian‐Ye</creatorcontrib><creatorcontrib>Liu, Xun‐Cheng</creatorcontrib><creatorcontrib>Han, Yan‐Chao</creatorcontrib><creatorcontrib>Xiao, Yun‐Yi</creatorcontrib><creatorcontrib>Shan, Wei</creatorcontrib><creatorcontrib>Tang, Yang</creatorcontrib><creatorcontrib>Wu, Ke‐Qiang</creatorcontrib><creatorcontrib>He, Jun‐Xian</creatorcontrib><creatorcontrib>Lu, Wang‐Jin</creatorcontrib><title>The transcriptional regulatory network mediated by banana (Musa acuminata) dehydration-responsive element binding (MaDREB) transcription factors in fruit ripening</title><title>The New phytologist</title><addtitle>New Phytol</addtitle><description>Fruit ripening is a complex, genetically programmed process involving the action of critical transcription factors (TFs). Despite the established significance of dehydration-responsive element binding (DREB) TFs in plant abiotic stress responses, the involvement of DREBs in fruit ripening is yet to be determined.
Here, we identified four genes encoding ripening-regulated DREB TFs in banana (Musa acuminata), MaDREB1, MaDREB2, MaDREB3, and MaDREB4, and demonstrated that they play regulatory roles in fruit ripening.
We showed that MaDREB1–MaDREB4 are nucleus-localized, induced by ethylene and encompass transcriptional activation activities. We performed a genome-wide chromatin immunoprecipitation and high-throughput sequencing (ChIP-Seq) experiment for MaDREB2 and identified 697 genomic regions as potential targets of MaDREB2. MaDREB2 binds to hundreds of loci with diverse functions and its binding sites are distributed in the promoter regions proximal to the transcriptional start site (TSS). Most of the MaDREB2-binding targets contain the conserved (A/G)CC(G/C)AC motif and MaDREB2 appears to directly regulate the expression of a number of genes involved in fruit ripening. In combination with transcriptome profiling (RNA sequencing) data, our results indicate that MaDREB2 may serve as both transcriptional activator and repressor during banana fruit ripening.
In conclusion, our study suggests a hierarchical regulatory model of fruit ripening in banana and that the MaDREB TFs may act as transcriptional regulators in the regulatory network.</description><subject>banana</subject><subject>Base Sequence</subject><subject>Binding sites</subject><subject>Cell Wall - metabolism</subject><subject>Chromatin</subject><subject>chromatin immunoprecipitation coupled DNA sequencing (ChIP‐Seq)</subject><subject>Dehydration</subject><subject>dehydration‐responsive element binding (DREB)</subject><subject>Down-Regulation - genetics</subject><subject>Fruit - genetics</subject><subject>Fruit - physiology</subject><subject>fruit ripening</subject><subject>Fruits</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Plant</subject><subject>Gene Regulatory Networks - genetics</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>Genes, Plant</subject><subject>Genomes</subject><subject>Identification</subject><subject>Immunoprecipitation</subject><subject>Musa</subject><subject>Musa - genetics</subject><subject>Musa - physiology</subject><subject>Musa acuminata</subject><subject>Next-generation sequencing</subject><subject>Nuclei</subject><subject>Nucleic acids</subject><subject>Nucleotide Motifs - genetics</subject><subject>Nucleus</subject><subject>Plant Proteins - isolation & purification</subject><subject>Plant Proteins - metabolism</subject><subject>Promoter Regions, Genetic - genetics</subject><subject>Promoters</subject><subject>Protein Binding - genetics</subject><subject>Regions</subject><subject>Regulators</subject><subject>Regulatory sequences</subject><subject>Ribonucleic acid</subject><subject>Ripening</subject><subject>RNA</subject><subject>RNA sequencing</subject><subject>Sequencing</subject><subject>Subcellular Fractions - metabolism</subject><subject>Transcription</subject><subject>Transcription activation</subject><subject>Transcription factors</subject><subject>Transcription Factors - isolation & purification</subject><subject>Transcription Factors - metabolism</subject><subject>Transcriptional Activation - genetics</subject><subject>transcriptional regulation</subject><issn>0028-646X</issn><issn>1469-8137</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl1rFTEQhoMo9li98AcoAW96LrbN137kUmu1Qv1AKni3ZDezPTnuZtcka9m_4y91jqctKAhmAhnIM--QeUPIU86OOa4TP22OuZKVvkdWXBU6q7gs75MVY6LKClV8PSCPYtwyxnReiIfkQFRMKcnlivy83ABNwfjYBjclN3rT0wBXc2_SGBbqIV2P4RsdwDqTwNJmoY3xGPTo_RwNNe08OG-SWVMLm8UGsxPJAsRp9NH9AAo9DOATbZy3zl9hnXn9-ezV-s-2tDMtdozUYRpmlyhegMeCx-RBZ_oIT27OQ_Llzdnl6Xl28fHtu9OXF1mLb9GZzkumJUgrSs6KTilrGlNpK43kPJdKNtyWhbZclbDLhdQ4GlGqXPEyV508JEd73SmM32eIqR5cbKHvjYdxjjWvqkojrtV_oHnOilwIjeiLv9DtOAecMlJaaYYhJFLrPdWGMcYAXT0FN5iw1JzVO49r9Lj-7TGyz28U5wZtuSNvTUXgZA9cux6WfyvVHz6d30o-21dsI3pwV6Hxxwjc8heSorrk</recordid><startdate>20170401</startdate><enddate>20170401</enddate><creator>Kuang, Jian‐Fei</creator><creator>Chen, Jian‐Ye</creator><creator>Liu, Xun‐Cheng</creator><creator>Han, Yan‐Chao</creator><creator>Xiao, Yun‐Yi</creator><creator>Shan, Wei</creator><creator>Tang, Yang</creator><creator>Wu, Ke‐Qiang</creator><creator>He, Jun‐Xian</creator><creator>Lu, Wang‐Jin</creator><general>New Phytologist Trust</general><general>Wiley Subscription Services, Inc</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>7QO</scope><scope>7SN</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7TM</scope></search><sort><creationdate>20170401</creationdate><title>The transcriptional regulatory network mediated by banana (Musa acuminata) dehydration-responsive element binding (MaDREB) transcription factors in fruit ripening</title><author>Kuang, Jian‐Fei ; Chen, Jian‐Ye ; Liu, Xun‐Cheng ; Han, Yan‐Chao ; Xiao, Yun‐Yi ; Shan, Wei ; Tang, Yang ; Wu, Ke‐Qiang ; He, Jun‐Xian ; Lu, Wang‐Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4439-957093e3d27106f44daba89d3a3115343b1d769d147e3b1d239646274541754f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>banana</topic><topic>Base Sequence</topic><topic>Binding sites</topic><topic>Cell Wall - metabolism</topic><topic>Chromatin</topic><topic>chromatin immunoprecipitation coupled DNA sequencing (ChIP‐Seq)</topic><topic>Dehydration</topic><topic>dehydration‐responsive element binding (DREB)</topic><topic>Down-Regulation - genetics</topic><topic>Fruit - genetics</topic><topic>Fruit - physiology</topic><topic>fruit ripening</topic><topic>Fruits</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Plant</topic><topic>Gene Regulatory Networks - genetics</topic><topic>Gene sequencing</topic><topic>Genes</topic><topic>Genes, Plant</topic><topic>Genomes</topic><topic>Identification</topic><topic>Immunoprecipitation</topic><topic>Musa</topic><topic>Musa - genetics</topic><topic>Musa - physiology</topic><topic>Musa acuminata</topic><topic>Next-generation sequencing</topic><topic>Nuclei</topic><topic>Nucleic acids</topic><topic>Nucleotide Motifs - genetics</topic><topic>Nucleus</topic><topic>Plant Proteins - isolation & purification</topic><topic>Plant Proteins - metabolism</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>Promoters</topic><topic>Protein Binding - genetics</topic><topic>Regions</topic><topic>Regulators</topic><topic>Regulatory sequences</topic><topic>Ribonucleic acid</topic><topic>Ripening</topic><topic>RNA</topic><topic>RNA sequencing</topic><topic>Sequencing</topic><topic>Subcellular Fractions - metabolism</topic><topic>Transcription</topic><topic>Transcription activation</topic><topic>Transcription factors</topic><topic>Transcription Factors - isolation & purification</topic><topic>Transcription Factors - metabolism</topic><topic>Transcriptional Activation - genetics</topic><topic>transcriptional regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kuang, Jian‐Fei</creatorcontrib><creatorcontrib>Chen, Jian‐Ye</creatorcontrib><creatorcontrib>Liu, Xun‐Cheng</creatorcontrib><creatorcontrib>Han, Yan‐Chao</creatorcontrib><creatorcontrib>Xiao, Yun‐Yi</creatorcontrib><creatorcontrib>Shan, Wei</creatorcontrib><creatorcontrib>Tang, Yang</creatorcontrib><creatorcontrib>Wu, Ke‐Qiang</creatorcontrib><creatorcontrib>He, Jun‐Xian</creatorcontrib><creatorcontrib>Lu, Wang‐Jin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Nucleic Acids Abstracts</collection><jtitle>The New phytologist</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kuang, Jian‐Fei</au><au>Chen, Jian‐Ye</au><au>Liu, Xun‐Cheng</au><au>Han, Yan‐Chao</au><au>Xiao, Yun‐Yi</au><au>Shan, Wei</au><au>Tang, Yang</au><au>Wu, Ke‐Qiang</au><au>He, Jun‐Xian</au><au>Lu, Wang‐Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The transcriptional regulatory network mediated by banana (Musa acuminata) dehydration-responsive element binding (MaDREB) transcription factors in fruit ripening</atitle><jtitle>The New phytologist</jtitle><addtitle>New Phytol</addtitle><date>2017-04-01</date><risdate>2017</risdate><volume>214</volume><issue>2</issue><spage>762</spage><epage>781</epage><pages>762-781</pages><issn>0028-646X</issn><eissn>1469-8137</eissn><abstract>Fruit ripening is a complex, genetically programmed process involving the action of critical transcription factors (TFs). Despite the established significance of dehydration-responsive element binding (DREB) TFs in plant abiotic stress responses, the involvement of DREBs in fruit ripening is yet to be determined.
Here, we identified four genes encoding ripening-regulated DREB TFs in banana (Musa acuminata), MaDREB1, MaDREB2, MaDREB3, and MaDREB4, and demonstrated that they play regulatory roles in fruit ripening.
We showed that MaDREB1–MaDREB4 are nucleus-localized, induced by ethylene and encompass transcriptional activation activities. We performed a genome-wide chromatin immunoprecipitation and high-throughput sequencing (ChIP-Seq) experiment for MaDREB2 and identified 697 genomic regions as potential targets of MaDREB2. MaDREB2 binds to hundreds of loci with diverse functions and its binding sites are distributed in the promoter regions proximal to the transcriptional start site (TSS). Most of the MaDREB2-binding targets contain the conserved (A/G)CC(G/C)AC motif and MaDREB2 appears to directly regulate the expression of a number of genes involved in fruit ripening. In combination with transcriptome profiling (RNA sequencing) data, our results indicate that MaDREB2 may serve as both transcriptional activator and repressor during banana fruit ripening.
In conclusion, our study suggests a hierarchical regulatory model of fruit ripening in banana and that the MaDREB TFs may act as transcriptional regulators in the regulatory network.</abstract><cop>England</cop><pub>New Phytologist Trust</pub><pmid>28044313</pmid><doi>10.1111/nph.14389</doi><tpages>20</tpages><oa>free_for_read</oa></addata></record> |
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subjects | banana Base Sequence Binding sites Cell Wall - metabolism Chromatin chromatin immunoprecipitation coupled DNA sequencing (ChIP‐Seq) Dehydration dehydration‐responsive element binding (DREB) Down-Regulation - genetics Fruit - genetics Fruit - physiology fruit ripening Fruits Gene expression Gene Expression Regulation, Plant Gene Regulatory Networks - genetics Gene sequencing Genes Genes, Plant Genomes Identification Immunoprecipitation Musa Musa - genetics Musa - physiology Musa acuminata Next-generation sequencing Nuclei Nucleic acids Nucleotide Motifs - genetics Nucleus Plant Proteins - isolation & purification Plant Proteins - metabolism Promoter Regions, Genetic - genetics Promoters Protein Binding - genetics Regions Regulators Regulatory sequences Ribonucleic acid Ripening RNA RNA sequencing Sequencing Subcellular Fractions - metabolism Transcription Transcription activation Transcription factors Transcription Factors - isolation & purification Transcription Factors - metabolism Transcriptional Activation - genetics transcriptional regulation |
title | The transcriptional regulatory network mediated by banana (Musa acuminata) dehydration-responsive element binding (MaDREB) transcription factors in fruit ripening |
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