Daily heliotropic movements assist gas exchange and productive responses in DREB1A soybean plants under drought stress in the greenhouse
Summary Drought stress is one of the most severe environmental constraints on plant production. Under environmental pressures, complex daily heliotropic adjustments of leaflet angles in soybean can help to reduce transpiration losses by diminishing light interception (paraheliotropism), increase diu...
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creator | Rakocevic, Miroslava Müller, Mariele Matsunaga, Fabio Takeshi Neumaier, Norman Farias, José Renato Bouças Nepomuceno, Alexandre Lima Fuganti‐Pagliarini, Renata |
description | Summary
Drought stress is one of the most severe environmental constraints on plant production. Under environmental pressures, complex daily heliotropic adjustments of leaflet angles in soybean can help to reduce transpiration losses by diminishing light interception (paraheliotropism), increase diurnal carbon gain in sparse canopies and reduce carbon gain in dense canopies by solar tracking (diaheliotropism). The plant materials studied were cultivar BR 16 and its genetically engineered isoline P58, ectopically overexpressing AtDREB1A, which is involved in abiotic stress responses. We aimed to follow the movements of central and lateral leaflets in vegetative stages V7–V10 and reproductive stages R4–R5, integrating the reversible morphogenetic changes into an estimate of daily plant photosynthesis using three‐dimensional modeling, and to analyze the production parameters of BR 16 and P58. The patterns of daily movements of central leaflets of BR 16 in V7–V10 and R4–R5 were similar, expressing fewer diaheliotropic movements under drought stress than under non‐limiting water conditions. Daily heliotropic patterns of lateral leaflets in V7–V10 and R4–R5 showed more diaheliotropic movements in drought‐stressed P58 plants than in those grown under non‐limiting water conditions. Leaf area in R4–R5 was generally higher in P58 than in BR 16. Drought significantly affected gas exchange and vegetative and reproductive architectural features. DREB1A could be involved in various responses to drought stress. Compared with the parental BR 16, P58 copes with drought through better compensation between diaheliotropic and paraheliotropic movements, finer tuning of water‐use efficiency, a lower transpiration rate, higher leaf area and higher pod abortion to accomplish the maximum possible grain production under continued drought conditions.
Significance Statement
DREB1A could be involved in various responses of soybean to drought stress, considering that the genetically modified isoline P58 was less drought sensitive than the parental BR 16, observed by a lower transpiration rate, a lower reduction in stomatal conductance, finer tuning of water‐use efficiency, a greater leaf area and better compensation between diaheliotropic and paraheliotropic movements. P58 showed higher pod abortion than parental BR 16 to achieve the maximum possible grain production under continued drought conditions. |
doi_str_mv | 10.1111/tpj.14069 |
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Drought stress is one of the most severe environmental constraints on plant production. Under environmental pressures, complex daily heliotropic adjustments of leaflet angles in soybean can help to reduce transpiration losses by diminishing light interception (paraheliotropism), increase diurnal carbon gain in sparse canopies and reduce carbon gain in dense canopies by solar tracking (diaheliotropism). The plant materials studied were cultivar BR 16 and its genetically engineered isoline P58, ectopically overexpressing AtDREB1A, which is involved in abiotic stress responses. We aimed to follow the movements of central and lateral leaflets in vegetative stages V7–V10 and reproductive stages R4–R5, integrating the reversible morphogenetic changes into an estimate of daily plant photosynthesis using three‐dimensional modeling, and to analyze the production parameters of BR 16 and P58. The patterns of daily movements of central leaflets of BR 16 in V7–V10 and R4–R5 were similar, expressing fewer diaheliotropic movements under drought stress than under non‐limiting water conditions. Daily heliotropic patterns of lateral leaflets in V7–V10 and R4–R5 showed more diaheliotropic movements in drought‐stressed P58 plants than in those grown under non‐limiting water conditions. Leaf area in R4–R5 was generally higher in P58 than in BR 16. Drought significantly affected gas exchange and vegetative and reproductive architectural features. DREB1A could be involved in various responses to drought stress. Compared with the parental BR 16, P58 copes with drought through better compensation between diaheliotropic and paraheliotropic movements, finer tuning of water‐use efficiency, a lower transpiration rate, higher leaf area and higher pod abortion to accomplish the maximum possible grain production under continued drought conditions.
Significance Statement
DREB1A could be involved in various responses of soybean to drought stress, considering that the genetically modified isoline P58 was less drought sensitive than the parental BR 16, observed by a lower transpiration rate, a lower reduction in stomatal conductance, finer tuning of water‐use efficiency, a greater leaf area and better compensation between diaheliotropic and paraheliotropic movements. P58 showed higher pod abortion than parental BR 16 to achieve the maximum possible grain production under continued drought conditions.</description><identifier>ISSN: 0960-7412</identifier><identifier>EISSN: 1365-313X</identifier><identifier>DOI: 10.1111/tpj.14069</identifier><identifier>PMID: 30118573</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Canopies ; Carbon ; Constraining ; Cultivars ; diaheliotropic ; Dimensional analysis ; Diurnal ; DREB1A ; Drought ; Droughts ; Gas exchange ; Gene Expression Regulation, Plant ; Genetic engineering ; Glycine max - genetics ; Glycine max - metabolism ; Grain ; Interception ; Leaf area ; Leaves ; Light interception ; paraheliotropic ; Photosynthesis ; Photosynthesis - genetics ; Plant Development - genetics ; Plant growth ; Plant Leaves - metabolism ; Plant production ; Plants, Genetically Modified - genetics ; Plants, Genetically Modified - metabolism ; pod production ; Soybean Proteins - genetics ; Soybean Proteins - metabolism ; Soybeans ; stomatal conductance ; Stress, Physiological - genetics ; Stresses ; Transpiration ; water‐use efficiency</subject><ispartof>The Plant journal : for cell and molecular biology, 2018-11, Vol.96 (4), p.801-814</ispartof><rights>2018 The Authors The Plant Journal © 2018 John Wiley & Sons Ltd</rights><rights>2018 The Authors The Plant Journal © 2018 John Wiley & Sons Ltd.</rights><rights>Copyright © 2018 John Wiley & Sons Ltd and the Society for Experimental Biology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-1898-5042 ; 0000-0001-9282-2826 ; 0000-0002-1648-8771 ; 0000-0002-3166-725X ; 0000-0002-2068-8821 ; 0000-0002-2544-1107 ; 0000-0003-2012-6201</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%2Ftpj.14069$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftpj.14069$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27903,27904,45553,45554,46387,46811</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30118573$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rakocevic, Miroslava</creatorcontrib><creatorcontrib>Müller, Mariele</creatorcontrib><creatorcontrib>Matsunaga, Fabio Takeshi</creatorcontrib><creatorcontrib>Neumaier, Norman</creatorcontrib><creatorcontrib>Farias, José Renato Bouças</creatorcontrib><creatorcontrib>Nepomuceno, Alexandre Lima</creatorcontrib><creatorcontrib>Fuganti‐Pagliarini, Renata</creatorcontrib><title>Daily heliotropic movements assist gas exchange and productive responses in DREB1A soybean plants under drought stress in the greenhouse</title><title>The Plant journal : for cell and molecular biology</title><addtitle>Plant J</addtitle><description>Summary
Drought stress is one of the most severe environmental constraints on plant production. Under environmental pressures, complex daily heliotropic adjustments of leaflet angles in soybean can help to reduce transpiration losses by diminishing light interception (paraheliotropism), increase diurnal carbon gain in sparse canopies and reduce carbon gain in dense canopies by solar tracking (diaheliotropism). The plant materials studied were cultivar BR 16 and its genetically engineered isoline P58, ectopically overexpressing AtDREB1A, which is involved in abiotic stress responses. We aimed to follow the movements of central and lateral leaflets in vegetative stages V7–V10 and reproductive stages R4–R5, integrating the reversible morphogenetic changes into an estimate of daily plant photosynthesis using three‐dimensional modeling, and to analyze the production parameters of BR 16 and P58. The patterns of daily movements of central leaflets of BR 16 in V7–V10 and R4–R5 were similar, expressing fewer diaheliotropic movements under drought stress than under non‐limiting water conditions. Daily heliotropic patterns of lateral leaflets in V7–V10 and R4–R5 showed more diaheliotropic movements in drought‐stressed P58 plants than in those grown under non‐limiting water conditions. Leaf area in R4–R5 was generally higher in P58 than in BR 16. Drought significantly affected gas exchange and vegetative and reproductive architectural features. DREB1A could be involved in various responses to drought stress. Compared with the parental BR 16, P58 copes with drought through better compensation between diaheliotropic and paraheliotropic movements, finer tuning of water‐use efficiency, a lower transpiration rate, higher leaf area and higher pod abortion to accomplish the maximum possible grain production under continued drought conditions.
Significance Statement
DREB1A could be involved in various responses of soybean to drought stress, considering that the genetically modified isoline P58 was less drought sensitive than the parental BR 16, observed by a lower transpiration rate, a lower reduction in stomatal conductance, finer tuning of water‐use efficiency, a greater leaf area and better compensation between diaheliotropic and paraheliotropic movements. P58 showed higher pod abortion than parental BR 16 to achieve the maximum possible grain production under continued drought conditions.</description><subject>Canopies</subject><subject>Carbon</subject><subject>Constraining</subject><subject>Cultivars</subject><subject>diaheliotropic</subject><subject>Dimensional analysis</subject><subject>Diurnal</subject><subject>DREB1A</subject><subject>Drought</subject><subject>Droughts</subject><subject>Gas exchange</subject><subject>Gene Expression Regulation, Plant</subject><subject>Genetic engineering</subject><subject>Glycine max - genetics</subject><subject>Glycine max - metabolism</subject><subject>Grain</subject><subject>Interception</subject><subject>Leaf area</subject><subject>Leaves</subject><subject>Light interception</subject><subject>paraheliotropic</subject><subject>Photosynthesis</subject><subject>Photosynthesis - genetics</subject><subject>Plant Development - genetics</subject><subject>Plant growth</subject><subject>Plant Leaves - metabolism</subject><subject>Plant production</subject><subject>Plants, Genetically Modified - genetics</subject><subject>Plants, Genetically Modified - metabolism</subject><subject>pod production</subject><subject>Soybean Proteins - genetics</subject><subject>Soybean Proteins - metabolism</subject><subject>Soybeans</subject><subject>stomatal conductance</subject><subject>Stress, Physiological - genetics</subject><subject>Stresses</subject><subject>Transpiration</subject><subject>water‐use efficiency</subject><issn>0960-7412</issn><issn>1365-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc9uFDEMxiMEotvCgRdAkbhwmTb_JtkcS1sKqBIIFYlblJl4d7KaSYYkU9g34LFJt4UDvtiSf7Y--0PoFSWntMZZmXenVBCpn6AV5bJtOOXfn6IV0ZI0SlB2hI5z3hFCFZfiOTrihNJ1q_gK_b60ftzjAUYfS4qz7_EU72CCUDK2Oftc8NZmDL_6wYYtYBscnlN0S1_8HeAEeY4hQ8Y-4MuvV-_oOc5x34ENeB7t_ZYlOEjYpbhsh4JzqSMHugyAtwkgDHHJ8AI929gxw8vHfIK-vb-6vfjQ3Hy-_nhxftPMnArdCG410b0SoutlrzdANrKTnLC1U72qTeaUY1x0nQLVblrhas2pcwys1ZrzE_T2YW894scCuZjJ5x7GqhWqDsPIWq9bKYWo6Jv_0F1cUqjqDKOcMUFariv1-pFaugmcmZOfbNqbvz-uwNkD8NOPsP_Xp8Tcm2eqeeZgnrn98ulQ8D8bFY3A</recordid><startdate>201811</startdate><enddate>201811</enddate><creator>Rakocevic, Miroslava</creator><creator>Müller, Mariele</creator><creator>Matsunaga, Fabio Takeshi</creator><creator>Neumaier, Norman</creator><creator>Farias, José Renato Bouças</creator><creator>Nepomuceno, Alexandre Lima</creator><creator>Fuganti‐Pagliarini, Renata</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1898-5042</orcidid><orcidid>https://orcid.org/0000-0001-9282-2826</orcidid><orcidid>https://orcid.org/0000-0002-1648-8771</orcidid><orcidid>https://orcid.org/0000-0002-3166-725X</orcidid><orcidid>https://orcid.org/0000-0002-2068-8821</orcidid><orcidid>https://orcid.org/0000-0002-2544-1107</orcidid><orcidid>https://orcid.org/0000-0003-2012-6201</orcidid></search><sort><creationdate>201811</creationdate><title>Daily heliotropic movements assist gas exchange and productive responses in DREB1A soybean plants under drought stress in the greenhouse</title><author>Rakocevic, Miroslava ; Müller, Mariele ; Matsunaga, Fabio Takeshi ; Neumaier, Norman ; Farias, José Renato Bouças ; Nepomuceno, Alexandre Lima ; Fuganti‐Pagliarini, Renata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p3149-43a909c744bc6c9fe0f6b63028d7c73a92d7d234bb7e75f54d34b31dd2eaa9933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Canopies</topic><topic>Carbon</topic><topic>Constraining</topic><topic>Cultivars</topic><topic>diaheliotropic</topic><topic>Dimensional analysis</topic><topic>Diurnal</topic><topic>DREB1A</topic><topic>Drought</topic><topic>Droughts</topic><topic>Gas exchange</topic><topic>Gene Expression Regulation, Plant</topic><topic>Genetic engineering</topic><topic>Glycine max - genetics</topic><topic>Glycine max - metabolism</topic><topic>Grain</topic><topic>Interception</topic><topic>Leaf area</topic><topic>Leaves</topic><topic>Light interception</topic><topic>paraheliotropic</topic><topic>Photosynthesis</topic><topic>Photosynthesis - genetics</topic><topic>Plant Development - genetics</topic><topic>Plant growth</topic><topic>Plant Leaves - metabolism</topic><topic>Plant production</topic><topic>Plants, Genetically Modified - genetics</topic><topic>Plants, Genetically Modified - metabolism</topic><topic>pod production</topic><topic>Soybean Proteins - genetics</topic><topic>Soybean Proteins - metabolism</topic><topic>Soybeans</topic><topic>stomatal conductance</topic><topic>Stress, Physiological - genetics</topic><topic>Stresses</topic><topic>Transpiration</topic><topic>water‐use efficiency</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rakocevic, Miroslava</creatorcontrib><creatorcontrib>Müller, Mariele</creatorcontrib><creatorcontrib>Matsunaga, Fabio Takeshi</creatorcontrib><creatorcontrib>Neumaier, Norman</creatorcontrib><creatorcontrib>Farias, José Renato Bouças</creatorcontrib><creatorcontrib>Nepomuceno, Alexandre Lima</creatorcontrib><creatorcontrib>Fuganti‐Pagliarini, Renata</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Plant journal : for cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rakocevic, Miroslava</au><au>Müller, Mariele</au><au>Matsunaga, Fabio Takeshi</au><au>Neumaier, Norman</au><au>Farias, José Renato Bouças</au><au>Nepomuceno, Alexandre Lima</au><au>Fuganti‐Pagliarini, Renata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Daily heliotropic movements assist gas exchange and productive responses in DREB1A soybean plants under drought stress in the greenhouse</atitle><jtitle>The Plant journal : for cell and molecular biology</jtitle><addtitle>Plant J</addtitle><date>2018-11</date><risdate>2018</risdate><volume>96</volume><issue>4</issue><spage>801</spage><epage>814</epage><pages>801-814</pages><issn>0960-7412</issn><eissn>1365-313X</eissn><abstract>Summary
Drought stress is one of the most severe environmental constraints on plant production. Under environmental pressures, complex daily heliotropic adjustments of leaflet angles in soybean can help to reduce transpiration losses by diminishing light interception (paraheliotropism), increase diurnal carbon gain in sparse canopies and reduce carbon gain in dense canopies by solar tracking (diaheliotropism). The plant materials studied were cultivar BR 16 and its genetically engineered isoline P58, ectopically overexpressing AtDREB1A, which is involved in abiotic stress responses. We aimed to follow the movements of central and lateral leaflets in vegetative stages V7–V10 and reproductive stages R4–R5, integrating the reversible morphogenetic changes into an estimate of daily plant photosynthesis using three‐dimensional modeling, and to analyze the production parameters of BR 16 and P58. The patterns of daily movements of central leaflets of BR 16 in V7–V10 and R4–R5 were similar, expressing fewer diaheliotropic movements under drought stress than under non‐limiting water conditions. Daily heliotropic patterns of lateral leaflets in V7–V10 and R4–R5 showed more diaheliotropic movements in drought‐stressed P58 plants than in those grown under non‐limiting water conditions. Leaf area in R4–R5 was generally higher in P58 than in BR 16. Drought significantly affected gas exchange and vegetative and reproductive architectural features. DREB1A could be involved in various responses to drought stress. Compared with the parental BR 16, P58 copes with drought through better compensation between diaheliotropic and paraheliotropic movements, finer tuning of water‐use efficiency, a lower transpiration rate, higher leaf area and higher pod abortion to accomplish the maximum possible grain production under continued drought conditions.
Significance Statement
DREB1A could be involved in various responses of soybean to drought stress, considering that the genetically modified isoline P58 was less drought sensitive than the parental BR 16, observed by a lower transpiration rate, a lower reduction in stomatal conductance, finer tuning of water‐use efficiency, a greater leaf area and better compensation between diaheliotropic and paraheliotropic movements. P58 showed higher pod abortion than parental BR 16 to achieve the maximum possible grain production under continued drought conditions.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>30118573</pmid><doi>10.1111/tpj.14069</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1898-5042</orcidid><orcidid>https://orcid.org/0000-0001-9282-2826</orcidid><orcidid>https://orcid.org/0000-0002-1648-8771</orcidid><orcidid>https://orcid.org/0000-0002-3166-725X</orcidid><orcidid>https://orcid.org/0000-0002-2068-8821</orcidid><orcidid>https://orcid.org/0000-0002-2544-1107</orcidid><orcidid>https://orcid.org/0000-0003-2012-6201</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Canopies Carbon Constraining Cultivars diaheliotropic Dimensional analysis Diurnal DREB1A Drought Droughts Gas exchange Gene Expression Regulation, Plant Genetic engineering Glycine max - genetics Glycine max - metabolism Grain Interception Leaf area Leaves Light interception paraheliotropic Photosynthesis Photosynthesis - genetics Plant Development - genetics Plant growth Plant Leaves - metabolism Plant production Plants, Genetically Modified - genetics Plants, Genetically Modified - metabolism pod production Soybean Proteins - genetics Soybean Proteins - metabolism Soybeans stomatal conductance Stress, Physiological - genetics Stresses Transpiration water‐use efficiency |
title | Daily heliotropic movements assist gas exchange and productive responses in DREB1A soybean plants under drought stress in the greenhouse |
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