Leaf morphology, rather than plant water status, underlies genetic variation of rice leaf rolling under drought
Soil drying causes leaf rolling in rice, but the relationship between leaf rolling and drought tolerance has historically confounded selection of drought‐tolerant genotypes. In this study on tropical japonica and aus diversity panels (170–220 genotypes), the degree of leaf rolling under drought was...
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description | Soil drying causes leaf rolling in rice, but the relationship between leaf rolling and drought tolerance has historically confounded selection of drought‐tolerant genotypes. In this study on tropical japonica and aus diversity panels (170–220 genotypes), the degree of leaf rolling under drought was more affected by leaf morphology than by stomatal conductance, leaf water status, or maintenance of shoot biomass and grain yield. A range of canopy temperature and leaf rolling (measured as change in normalized difference vegetation index [ΔNDVI]) combinations were observed among aus genotypes, indicating that some genotypes continued transpiration while rolled. Association mapping indicated colocation of genomic regions for leaf rolling score and ΔNDVI under drought with previously reported leaf rolling genes and gene networks related to leaf anatomy. The relatively subtle variation across these large diversity panels may explain the lack of agreement of this study with earlier reports that used small numbers of genotypes that were highly divergent in hydraulic traits driving leaf rolling differences. This study highlights the large range of physiological responses to drought among rice genotypes and emphasizes that drought response processes should be understood in detail before incorporating them into a varietal selection programme.
Leaf rolling was characterized in two rice diversity panels (aus and tropical japonica) under drought stress, either by visual scoring or by change in NDVI over successive dates. The phenotypic variation and identified candidate genes/networks related to leaf rolling under drought in two rice (Oryza sativa L.) diversity panels (aus and tropical japonica) showed stronger relationships with leaf morphology than with plant growth or grain yield under drought. These results help explain why selection for leaf rolling has historically confounded selection of genotypes with higher yield under drought. |
doi_str_mv | 10.1111/pce.13514 |
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Leaf rolling was characterized in two rice diversity panels (aus and tropical japonica) under drought stress, either by visual scoring or by change in NDVI over successive dates. The phenotypic variation and identified candidate genes/networks related to leaf rolling under drought in two rice (Oryza sativa L.) diversity panels (aus and tropical japonica) showed stronger relationships with leaf morphology than with plant growth or grain yield under drought. These results help explain why selection for leaf rolling has historically confounded selection of genotypes with higher yield under drought.</description><identifier>ISSN: 0140-7791</identifier><identifier>EISSN: 1365-3040</identifier><identifier>DOI: 10.1111/pce.13514</identifier><identifier>PMID: 30620079</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>aus ; biomass ; canopy ; chromosome mapping ; Conductance ; Crop yield ; Dehydration - genetics ; Drought ; Drought resistance ; drought tolerance ; Droughts ; Drying ; Gene mapping ; gene regulatory networks ; genes ; Genetic diversity ; Genetic Variation ; genomics ; Genotype ; Genotypes ; Genotyping Techniques ; grain yield ; leaf morphology ; leaf rolling ; Leaves ; Life Sciences ; Mapping ; Morphology ; normalized difference vegetation index ; Normalized difference vegetative index ; Original ; Oryza - genetics ; Oryza - metabolism ; Panels ; Phenotype ; physiological response ; Physiological responses ; Plant Leaves - anatomy & histology ; Plant Leaves - genetics ; Plant Leaves - physiology ; Polymorphism, Single Nucleotide - genetics ; Resistance ; Rice ; soil ; Stomata ; Stomatal conductance ; Stress, Physiological - genetics ; Stress, Physiological - physiology ; temperature ; Transpiration ; tropical japonica ; Vegetal Biology ; Water - physiology</subject><ispartof>Plant, cell and environment, 2019-05, Vol.42 (5), p.1532-1544</ispartof><rights>2019 The Authors Plant, Cell & Environment Published by John Wiley & Sons Ltd</rights><rights>2019 The Authors Plant, Cell & Environment Published by John Wiley & Sons Ltd.</rights><rights>2019 John Wiley & Sons Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5764-2910ccf2f65b384d1fcdd1a992baed13512468e0e3b3f11dccc1d7a57206a6a93</citedby><cites>FETCH-LOGICAL-c5764-2910ccf2f65b384d1fcdd1a992baed13512468e0e3b3f11dccc1d7a57206a6a93</cites><orcidid>0000-0002-1189-0673 ; 0000-0002-9472-3167 ; 0000-0001-6255-5480 ; 0000-0002-9613-5537 ; 0000-0002-2543-7140 ; 0000-0002-4369-5688</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%2Fpce.13514$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpce.13514$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30620079$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02620961$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Cal, Andrew J.</creatorcontrib><creatorcontrib>Sanciangco, Millicent</creatorcontrib><creatorcontrib>Rebolledo, Maria Camila</creatorcontrib><creatorcontrib>Luquet, Delphine</creatorcontrib><creatorcontrib>Torres, Rolando O.</creatorcontrib><creatorcontrib>McNally, Kenneth L.</creatorcontrib><creatorcontrib>Henry, Amelia</creatorcontrib><title>Leaf morphology, rather than plant water status, underlies genetic variation of rice leaf rolling under drought</title><title>Plant, cell and environment</title><addtitle>Plant Cell Environ</addtitle><description>Soil drying causes leaf rolling in rice, but the relationship between leaf rolling and drought tolerance has historically confounded selection of drought‐tolerant genotypes. In this study on tropical japonica and aus diversity panels (170–220 genotypes), the degree of leaf rolling under drought was more affected by leaf morphology than by stomatal conductance, leaf water status, or maintenance of shoot biomass and grain yield. A range of canopy temperature and leaf rolling (measured as change in normalized difference vegetation index [ΔNDVI]) combinations were observed among aus genotypes, indicating that some genotypes continued transpiration while rolled. Association mapping indicated colocation of genomic regions for leaf rolling score and ΔNDVI under drought with previously reported leaf rolling genes and gene networks related to leaf anatomy. The relatively subtle variation across these large diversity panels may explain the lack of agreement of this study with earlier reports that used small numbers of genotypes that were highly divergent in hydraulic traits driving leaf rolling differences. This study highlights the large range of physiological responses to drought among rice genotypes and emphasizes that drought response processes should be understood in detail before incorporating them into a varietal selection programme.
Leaf rolling was characterized in two rice diversity panels (aus and tropical japonica) under drought stress, either by visual scoring or by change in NDVI over successive dates. The phenotypic variation and identified candidate genes/networks related to leaf rolling under drought in two rice (Oryza sativa L.) diversity panels (aus and tropical japonica) showed stronger relationships with leaf morphology than with plant growth or grain yield under drought. These results help explain why selection for leaf rolling has historically confounded selection of genotypes with higher yield under drought.</description><subject>aus</subject><subject>biomass</subject><subject>canopy</subject><subject>chromosome mapping</subject><subject>Conductance</subject><subject>Crop yield</subject><subject>Dehydration - genetics</subject><subject>Drought</subject><subject>Drought resistance</subject><subject>drought tolerance</subject><subject>Droughts</subject><subject>Drying</subject><subject>Gene mapping</subject><subject>gene regulatory networks</subject><subject>genes</subject><subject>Genetic diversity</subject><subject>Genetic Variation</subject><subject>genomics</subject><subject>Genotype</subject><subject>Genotypes</subject><subject>Genotyping Techniques</subject><subject>grain yield</subject><subject>leaf morphology</subject><subject>leaf rolling</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Mapping</subject><subject>Morphology</subject><subject>normalized difference vegetation index</subject><subject>Normalized difference vegetative index</subject><subject>Original</subject><subject>Oryza - genetics</subject><subject>Oryza - metabolism</subject><subject>Panels</subject><subject>Phenotype</subject><subject>physiological response</subject><subject>Physiological responses</subject><subject>Plant Leaves - anatomy & histology</subject><subject>Plant Leaves - genetics</subject><subject>Plant Leaves - physiology</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Resistance</subject><subject>Rice</subject><subject>soil</subject><subject>Stomata</subject><subject>Stomatal conductance</subject><subject>Stress, Physiological - genetics</subject><subject>Stress, Physiological - physiology</subject><subject>temperature</subject><subject>Transpiration</subject><subject>tropical japonica</subject><subject>Vegetal Biology</subject><subject>Water - physiology</subject><issn>0140-7791</issn><issn>1365-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNqFklFrFDEUhYModq0--Ack4ItCp83NTDKTF6Es1QoL-qDPIZvJzKRkJ2OS2bL_3mynVi2IeQncfPfcm8NB6DWQc8jnYtLmHEoG1RO0gpKzoiQVeYpWBCpS1LWAE_QixhtCcqEWz9FJSTglpBYr5DdGdXjnwzR45_vDGQ4qDSbgNKgRT06NCd-qlAsxqTTHMzyPrQnOmoh7M5pkNd6rYFWyfsS-w8Fqg91RNHjn7NgvDbgNfu6H9BI965SL5tX9fYq-f7z6tr4uNl8-fV5fbgrNal4VVADRuqMdZ9uyqVrodNuCEoJulWmPf6UVbwwx5bbsAFqtNbS1YjUlXHElylP0YdGd5u3OtNqMKSgnp2B3KhykV1b-_TLaQfZ-L3nV1A3lWeD9IjA8aru-3MhjjdDsoeCwh8y-ux8W_I_ZxCR3NmrjsnvGz1HSEhhllN7J_gcFzkjFmaAZffsIvfFzGLNrklJSNwKqhv3eUwcfYzDdw7JA5DEdMqdD3qUjs2_-NOWB_BWHDFwswK115vBvJfl1fbVI_gSWQMQ6</recordid><startdate>201905</startdate><enddate>201905</enddate><creator>Cal, Andrew J.</creator><creator>Sanciangco, Millicent</creator><creator>Rebolledo, Maria Camila</creator><creator>Luquet, Delphine</creator><creator>Torres, Rolando O.</creator><creator>McNally, Kenneth L.</creator><creator>Henry, Amelia</creator><general>Wiley Subscription Services, Inc</general><general>Wiley</general><general>John Wiley and Sons Inc</general><scope>24P</scope><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>7QP</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1189-0673</orcidid><orcidid>https://orcid.org/0000-0002-9472-3167</orcidid><orcidid>https://orcid.org/0000-0001-6255-5480</orcidid><orcidid>https://orcid.org/0000-0002-9613-5537</orcidid><orcidid>https://orcid.org/0000-0002-2543-7140</orcidid><orcidid>https://orcid.org/0000-0002-4369-5688</orcidid></search><sort><creationdate>201905</creationdate><title>Leaf morphology, rather than plant water status, underlies genetic variation of rice leaf rolling under drought</title><author>Cal, Andrew J. ; Sanciangco, Millicent ; Rebolledo, Maria Camila ; Luquet, Delphine ; Torres, Rolando O. ; McNally, Kenneth L. ; Henry, Amelia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5764-2910ccf2f65b384d1fcdd1a992baed13512468e0e3b3f11dccc1d7a57206a6a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>aus</topic><topic>biomass</topic><topic>canopy</topic><topic>chromosome mapping</topic><topic>Conductance</topic><topic>Crop yield</topic><topic>Dehydration - genetics</topic><topic>Drought</topic><topic>Drought resistance</topic><topic>drought tolerance</topic><topic>Droughts</topic><topic>Drying</topic><topic>Gene mapping</topic><topic>gene regulatory networks</topic><topic>genes</topic><topic>Genetic diversity</topic><topic>Genetic Variation</topic><topic>genomics</topic><topic>Genotype</topic><topic>Genotypes</topic><topic>Genotyping Techniques</topic><topic>grain yield</topic><topic>leaf morphology</topic><topic>leaf rolling</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Mapping</topic><topic>Morphology</topic><topic>normalized difference vegetation index</topic><topic>Normalized difference vegetative index</topic><topic>Original</topic><topic>Oryza - genetics</topic><topic>Oryza - metabolism</topic><topic>Panels</topic><topic>Phenotype</topic><topic>physiological response</topic><topic>Physiological responses</topic><topic>Plant Leaves - anatomy & histology</topic><topic>Plant Leaves - genetics</topic><topic>Plant Leaves - physiology</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Resistance</topic><topic>Rice</topic><topic>soil</topic><topic>Stomata</topic><topic>Stomatal conductance</topic><topic>Stress, Physiological - genetics</topic><topic>Stress, Physiological - physiology</topic><topic>temperature</topic><topic>Transpiration</topic><topic>tropical japonica</topic><topic>Vegetal Biology</topic><topic>Water - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cal, Andrew J.</creatorcontrib><creatorcontrib>Sanciangco, Millicent</creatorcontrib><creatorcontrib>Rebolledo, Maria Camila</creatorcontrib><creatorcontrib>Luquet, Delphine</creatorcontrib><creatorcontrib>Torres, Rolando O.</creatorcontrib><creatorcontrib>McNally, Kenneth L.</creatorcontrib><creatorcontrib>Henry, Amelia</creatorcontrib><collection>Wiley Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant, cell and environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cal, Andrew J.</au><au>Sanciangco, Millicent</au><au>Rebolledo, Maria Camila</au><au>Luquet, Delphine</au><au>Torres, Rolando O.</au><au>McNally, Kenneth L.</au><au>Henry, Amelia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leaf morphology, rather than plant water status, underlies genetic variation of rice leaf rolling under drought</atitle><jtitle>Plant, cell and environment</jtitle><addtitle>Plant Cell Environ</addtitle><date>2019-05</date><risdate>2019</risdate><volume>42</volume><issue>5</issue><spage>1532</spage><epage>1544</epage><pages>1532-1544</pages><issn>0140-7791</issn><eissn>1365-3040</eissn><abstract>Soil drying causes leaf rolling in rice, but the relationship between leaf rolling and drought tolerance has historically confounded selection of drought‐tolerant genotypes. In this study on tropical japonica and aus diversity panels (170–220 genotypes), the degree of leaf rolling under drought was more affected by leaf morphology than by stomatal conductance, leaf water status, or maintenance of shoot biomass and grain yield. A range of canopy temperature and leaf rolling (measured as change in normalized difference vegetation index [ΔNDVI]) combinations were observed among aus genotypes, indicating that some genotypes continued transpiration while rolled. Association mapping indicated colocation of genomic regions for leaf rolling score and ΔNDVI under drought with previously reported leaf rolling genes and gene networks related to leaf anatomy. The relatively subtle variation across these large diversity panels may explain the lack of agreement of this study with earlier reports that used small numbers of genotypes that were highly divergent in hydraulic traits driving leaf rolling differences. This study highlights the large range of physiological responses to drought among rice genotypes and emphasizes that drought response processes should be understood in detail before incorporating them into a varietal selection programme.
Leaf rolling was characterized in two rice diversity panels (aus and tropical japonica) under drought stress, either by visual scoring or by change in NDVI over successive dates. The phenotypic variation and identified candidate genes/networks related to leaf rolling under drought in two rice (Oryza sativa L.) diversity panels (aus and tropical japonica) showed stronger relationships with leaf morphology than with plant growth or grain yield under drought. These results help explain why selection for leaf rolling has historically confounded selection of genotypes with higher yield under drought.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>30620079</pmid><doi>10.1111/pce.13514</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-1189-0673</orcidid><orcidid>https://orcid.org/0000-0002-9472-3167</orcidid><orcidid>https://orcid.org/0000-0001-6255-5480</orcidid><orcidid>https://orcid.org/0000-0002-9613-5537</orcidid><orcidid>https://orcid.org/0000-0002-2543-7140</orcidid><orcidid>https://orcid.org/0000-0002-4369-5688</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | aus biomass canopy chromosome mapping Conductance Crop yield Dehydration - genetics Drought Drought resistance drought tolerance Droughts Drying Gene mapping gene regulatory networks genes Genetic diversity Genetic Variation genomics Genotype Genotypes Genotyping Techniques grain yield leaf morphology leaf rolling Leaves Life Sciences Mapping Morphology normalized difference vegetation index Normalized difference vegetative index Original Oryza - genetics Oryza - metabolism Panels Phenotype physiological response Physiological responses Plant Leaves - anatomy & histology Plant Leaves - genetics Plant Leaves - physiology Polymorphism, Single Nucleotide - genetics Resistance Rice soil Stomata Stomatal conductance Stress, Physiological - genetics Stress, Physiological - physiology temperature Transpiration tropical japonica Vegetal Biology Water - physiology |
title | Leaf morphology, rather than plant water status, underlies genetic variation of rice leaf rolling under drought |
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