Transcriptome of Cenostigma pyramidale roots, a woody legume, under different salt stress times
Salinity stress has a significant impact on the gain of plant biomass. Our study provides the first root transcriptome of Cenostigma pyramidale, a tolerant woody legume from a tropical dry forest, under three different salt stress times (30 min, 2 h, and 11 days). The transcriptome was assembled usi...
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creator | Frosi, Gabriella Ferreira‐Neto, José Ribamar Costa Bezerra‐Neto, João Pacífico Pandolfi, Valesca Silva, Manassés Daniel Lima Morais, David Anderson Benko‐Iseppon, Ana Maria Santos, Mauro Guida |
description | Salinity stress has a significant impact on the gain of plant biomass. Our study provides the first root transcriptome of Cenostigma pyramidale, a tolerant woody legume from a tropical dry forest, under three different salt stress times (30 min, 2 h, and 11 days). The transcriptome was assembled using the RNA sequencing (RNA‐Seq) de novo pipeline from GenPipes. We observed 932, 804, and 3157 upregulated differentially expressed genes (DEGs) and 164, 273, and 1332 downregulated DEGs for salt over 30 min, 2 h, and 11 days, respectively. For DEGs annotated with the Viridiplantae clade in the early stress periods, the response to salt stress was mainly achieved by stabilizing homeostasis of such ions like Na+ and K+, signaling by Ca2+, transcription factor modulation, water transport, and oxidative stress. For salt stress at 11 days, we observed a higher modulation of transcription factors including the WRKY, MYB, bHLH, NAC, HSF, and AP2‐EREBP families, as well as DEGs involved in hormonal responses, water transport, sugar metabolism, proline, and reactive oxygen scavenging mechanisms. Five selected DEGs (K+ transporter, aquaporin, glutathione S‐transferase, cyclic nucleotide‐gated channel, and superoxide dismutase) were validated by qPCR. Our results indicated that C. pyramidale had an early perception of salt stress modulating ionic channels and transporters, and as the stress progressed, the focus turned to the antioxidant system, aquaporins, and complex hormone responses. The results of this first root transcriptome provide clues on how this native species modulate gene expression to achieve salt stress tolerance. |
doi_str_mv | 10.1111/ppl.13456 |
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Our study provides the first root transcriptome of Cenostigma pyramidale, a tolerant woody legume from a tropical dry forest, under three different salt stress times (30 min, 2 h, and 11 days). The transcriptome was assembled using the RNA sequencing (RNA‐Seq) de novo pipeline from GenPipes. We observed 932, 804, and 3157 upregulated differentially expressed genes (DEGs) and 164, 273, and 1332 downregulated DEGs for salt over 30 min, 2 h, and 11 days, respectively. For DEGs annotated with the Viridiplantae clade in the early stress periods, the response to salt stress was mainly achieved by stabilizing homeostasis of such ions like Na+ and K+, signaling by Ca2+, transcription factor modulation, water transport, and oxidative stress. For salt stress at 11 days, we observed a higher modulation of transcription factors including the WRKY, MYB, bHLH, NAC, HSF, and AP2‐EREBP families, as well as DEGs involved in hormonal responses, water transport, sugar metabolism, proline, and reactive oxygen scavenging mechanisms. Five selected DEGs (K+ transporter, aquaporin, glutathione S‐transferase, cyclic nucleotide‐gated channel, and superoxide dismutase) were validated by qPCR. Our results indicated that C. pyramidale had an early perception of salt stress modulating ionic channels and transporters, and as the stress progressed, the focus turned to the antioxidant system, aquaporins, and complex hormone responses. The results of this first root transcriptome provide clues on how this native species modulate gene expression to achieve salt stress tolerance.</description><identifier>ISSN: 0031-9317</identifier><identifier>EISSN: 1399-3054</identifier><identifier>DOI: 10.1111/ppl.13456</identifier><identifier>PMID: 33973275</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Abiotic stress ; Antioxidants ; Aquaporins ; Calcium ions ; Calcium signalling ; differential expression ; Dry forests ; Fabaceae ; Gene expression ; Gene sequencing ; Glutathione ; Homeostasis ; Indigenous species ; Legumes ; Modulation ; Nucleotides ; Osmosis ; Oxidative stress ; Plant biomass ; Proline ; Reactive oxygen species ; Ribonucleic acid ; RNA ; RNA‐Seq ; root physiology ; Salinity tolerance ; salt tolerance ; Salts ; Scavenging ; Superoxide dismutase ; Transcription factors ; Transcriptomes ; Tropical forests ; Water transport</subject><ispartof>Physiologia plantarum, 2021-12, Vol.173 (4), p.1463-1480</ispartof><rights>2021 Scandinavian Plant Physiology Society.</rights><rights>This article is protected by copyright. All rights reserved.</rights><rights>2021 Scandinavian Plant Physiology Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-d7470708bc02b1a36ba50208e84e3580b20b3f4562cf2ee2d6dad9943af5baf33</citedby><cites>FETCH-LOGICAL-c3536-d7470708bc02b1a36ba50208e84e3580b20b3f4562cf2ee2d6dad9943af5baf33</cites><orcidid>0000-0003-0935-203X ; 0000-0001-5146-4591</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fppl.13456$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fppl.13456$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33973275$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Frosi, Gabriella</creatorcontrib><creatorcontrib>Ferreira‐Neto, José Ribamar Costa</creatorcontrib><creatorcontrib>Bezerra‐Neto, João Pacífico</creatorcontrib><creatorcontrib>Pandolfi, Valesca</creatorcontrib><creatorcontrib>Silva, Manassés Daniel</creatorcontrib><creatorcontrib>Lima Morais, David Anderson</creatorcontrib><creatorcontrib>Benko‐Iseppon, Ana Maria</creatorcontrib><creatorcontrib>Santos, Mauro Guida</creatorcontrib><title>Transcriptome of Cenostigma pyramidale roots, a woody legume, under different salt stress times</title><title>Physiologia plantarum</title><addtitle>Physiol Plant</addtitle><description>Salinity stress has a significant impact on the gain of plant biomass. Our study provides the first root transcriptome of Cenostigma pyramidale, a tolerant woody legume from a tropical dry forest, under three different salt stress times (30 min, 2 h, and 11 days). The transcriptome was assembled using the RNA sequencing (RNA‐Seq) de novo pipeline from GenPipes. We observed 932, 804, and 3157 upregulated differentially expressed genes (DEGs) and 164, 273, and 1332 downregulated DEGs for salt over 30 min, 2 h, and 11 days, respectively. For DEGs annotated with the Viridiplantae clade in the early stress periods, the response to salt stress was mainly achieved by stabilizing homeostasis of such ions like Na+ and K+, signaling by Ca2+, transcription factor modulation, water transport, and oxidative stress. For salt stress at 11 days, we observed a higher modulation of transcription factors including the WRKY, MYB, bHLH, NAC, HSF, and AP2‐EREBP families, as well as DEGs involved in hormonal responses, water transport, sugar metabolism, proline, and reactive oxygen scavenging mechanisms. Five selected DEGs (K+ transporter, aquaporin, glutathione S‐transferase, cyclic nucleotide‐gated channel, and superoxide dismutase) were validated by qPCR. Our results indicated that C. pyramidale had an early perception of salt stress modulating ionic channels and transporters, and as the stress progressed, the focus turned to the antioxidant system, aquaporins, and complex hormone responses. The results of this first root transcriptome provide clues on how this native species modulate gene expression to achieve salt stress tolerance.</description><subject>Abiotic stress</subject><subject>Antioxidants</subject><subject>Aquaporins</subject><subject>Calcium ions</subject><subject>Calcium signalling</subject><subject>differential expression</subject><subject>Dry forests</subject><subject>Fabaceae</subject><subject>Gene expression</subject><subject>Gene sequencing</subject><subject>Glutathione</subject><subject>Homeostasis</subject><subject>Indigenous species</subject><subject>Legumes</subject><subject>Modulation</subject><subject>Nucleotides</subject><subject>Osmosis</subject><subject>Oxidative stress</subject><subject>Plant biomass</subject><subject>Proline</subject><subject>Reactive oxygen species</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>RNA‐Seq</subject><subject>root physiology</subject><subject>Salinity tolerance</subject><subject>salt tolerance</subject><subject>Salts</subject><subject>Scavenging</subject><subject>Superoxide dismutase</subject><subject>Transcription factors</subject><subject>Transcriptomes</subject><subject>Tropical forests</subject><subject>Water transport</subject><issn>0031-9317</issn><issn>1399-3054</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAQhoMouq4e_AMS8KJgNck0_TjK4hcsuIf1HNJmIpW2qUmL7L83uupBcA4zl2deZh5CTji74rGuh6G94pDKbIfMOJRlAkymu2TGGPCkBJ4fkMMQXhnjWcbFPjkAKHMQuZwRtfa6D7VvhtF1SJ2lC-xdGJuXTtNh43XXGN0i9c6N4ZJq-u6c2dAWX6YOL-nUG_TUNNaix36kQbexjR5DoGPTYTgie1a3AY-_55w8392uFw_J8un-cXGzTGqQkCUmT3OWs6Kqmai4hqzSkglWYJEiyIJVglVg44eitgJRmMxoU5YpaCsrbQHm5HybO3j3NmEYVdeEGttW9-imoIQUMpM8jytzcvYHfXWT7-N1SmQMSlHksozUxZaqvQvBo1WDbzrtN4oz9WldRevqy3pkT78Tp6pD80v-aI7A9RZ4b1rc_J-kVqvlNvIDpYuL4Q</recordid><startdate>202112</startdate><enddate>202112</enddate><creator>Frosi, Gabriella</creator><creator>Ferreira‐Neto, José Ribamar Costa</creator><creator>Bezerra‐Neto, João Pacífico</creator><creator>Pandolfi, Valesca</creator><creator>Silva, Manassés Daniel</creator><creator>Lima Morais, David Anderson</creator><creator>Benko‐Iseppon, Ana Maria</creator><creator>Santos, Mauro Guida</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7ST</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0935-203X</orcidid><orcidid>https://orcid.org/0000-0001-5146-4591</orcidid></search><sort><creationdate>202112</creationdate><title>Transcriptome of Cenostigma pyramidale roots, a woody legume, under different salt stress times</title><author>Frosi, Gabriella ; Ferreira‐Neto, José Ribamar Costa ; Bezerra‐Neto, João Pacífico ; Pandolfi, Valesca ; Silva, Manassés Daniel ; Lima Morais, David Anderson ; Benko‐Iseppon, Ana Maria ; Santos, Mauro Guida</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-d7470708bc02b1a36ba50208e84e3580b20b3f4562cf2ee2d6dad9943af5baf33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Abiotic stress</topic><topic>Antioxidants</topic><topic>Aquaporins</topic><topic>Calcium ions</topic><topic>Calcium signalling</topic><topic>differential expression</topic><topic>Dry forests</topic><topic>Fabaceae</topic><topic>Gene expression</topic><topic>Gene sequencing</topic><topic>Glutathione</topic><topic>Homeostasis</topic><topic>Indigenous species</topic><topic>Legumes</topic><topic>Modulation</topic><topic>Nucleotides</topic><topic>Osmosis</topic><topic>Oxidative stress</topic><topic>Plant biomass</topic><topic>Proline</topic><topic>Reactive oxygen species</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>RNA‐Seq</topic><topic>root physiology</topic><topic>Salinity tolerance</topic><topic>salt tolerance</topic><topic>Salts</topic><topic>Scavenging</topic><topic>Superoxide dismutase</topic><topic>Transcription factors</topic><topic>Transcriptomes</topic><topic>Tropical forests</topic><topic>Water transport</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Frosi, Gabriella</creatorcontrib><creatorcontrib>Ferreira‐Neto, José Ribamar Costa</creatorcontrib><creatorcontrib>Bezerra‐Neto, João Pacífico</creatorcontrib><creatorcontrib>Pandolfi, Valesca</creatorcontrib><creatorcontrib>Silva, Manassés Daniel</creatorcontrib><creatorcontrib>Lima Morais, David Anderson</creatorcontrib><creatorcontrib>Benko‐Iseppon, Ana Maria</creatorcontrib><creatorcontrib>Santos, Mauro Guida</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Physiologia plantarum</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Frosi, Gabriella</au><au>Ferreira‐Neto, José Ribamar Costa</au><au>Bezerra‐Neto, João Pacífico</au><au>Pandolfi, Valesca</au><au>Silva, Manassés Daniel</au><au>Lima Morais, David Anderson</au><au>Benko‐Iseppon, Ana Maria</au><au>Santos, Mauro Guida</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Transcriptome of Cenostigma pyramidale roots, a woody legume, under different salt stress times</atitle><jtitle>Physiologia plantarum</jtitle><addtitle>Physiol Plant</addtitle><date>2021-12</date><risdate>2021</risdate><volume>173</volume><issue>4</issue><spage>1463</spage><epage>1480</epage><pages>1463-1480</pages><issn>0031-9317</issn><eissn>1399-3054</eissn><abstract>Salinity stress has a significant impact on the gain of plant biomass. Our study provides the first root transcriptome of Cenostigma pyramidale, a tolerant woody legume from a tropical dry forest, under three different salt stress times (30 min, 2 h, and 11 days). The transcriptome was assembled using the RNA sequencing (RNA‐Seq) de novo pipeline from GenPipes. We observed 932, 804, and 3157 upregulated differentially expressed genes (DEGs) and 164, 273, and 1332 downregulated DEGs for salt over 30 min, 2 h, and 11 days, respectively. For DEGs annotated with the Viridiplantae clade in the early stress periods, the response to salt stress was mainly achieved by stabilizing homeostasis of such ions like Na+ and K+, signaling by Ca2+, transcription factor modulation, water transport, and oxidative stress. For salt stress at 11 days, we observed a higher modulation of transcription factors including the WRKY, MYB, bHLH, NAC, HSF, and AP2‐EREBP families, as well as DEGs involved in hormonal responses, water transport, sugar metabolism, proline, and reactive oxygen scavenging mechanisms. Five selected DEGs (K+ transporter, aquaporin, glutathione S‐transferase, cyclic nucleotide‐gated channel, and superoxide dismutase) were validated by qPCR. Our results indicated that C. pyramidale had an early perception of salt stress modulating ionic channels and transporters, and as the stress progressed, the focus turned to the antioxidant system, aquaporins, and complex hormone responses. The results of this first root transcriptome provide clues on how this native species modulate gene expression to achieve salt stress tolerance.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>33973275</pmid><doi>10.1111/ppl.13456</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-0935-203X</orcidid><orcidid>https://orcid.org/0000-0001-5146-4591</orcidid></addata></record> |
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subjects | Abiotic stress Antioxidants Aquaporins Calcium ions Calcium signalling differential expression Dry forests Fabaceae Gene expression Gene sequencing Glutathione Homeostasis Indigenous species Legumes Modulation Nucleotides Osmosis Oxidative stress Plant biomass Proline Reactive oxygen species Ribonucleic acid RNA RNA‐Seq root physiology Salinity tolerance salt tolerance Salts Scavenging Superoxide dismutase Transcription factors Transcriptomes Tropical forests Water transport |
title | Transcriptome of Cenostigma pyramidale roots, a woody legume, under different salt stress times |
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