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Difference in chilling-induced flavonoid profiles, antioxidant activity and chilling tolerance between soybean near-isogenic lines for the pubescence color gene
Chilling tolerance is an important trait of soybeans [Glycine max (L.) Merr.] produced in cool climates. We previously isolated a soybean flavonoid 3′ hydroxylase (F3′H) gene corresponding to the T locus, which controls pubescence and seed coat color. A genetic link between the T gene and chilling t...
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Published in: | Journal of plant research 2011-01, Vol.124 (1), p.173-182 |
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description | Chilling tolerance is an important trait of soybeans [Glycine max (L.) Merr.] produced in cool climates. We previously isolated a soybean flavonoid 3′ hydroxylase (F3′H) gene corresponding to the T locus, which controls pubescence and seed coat color. A genetic link between the T gene and chilling tolerance has been reported, although the exact underlying mechanisms remain unclear. Using the soybean near-isogenic lines (NILs) To7B (TT) and To7G (tt), we examined the relationship between chilling injury, antioxidant activity and flavonoid profiles associated with chilling treatment (15°C). Chilling injury was more severe in the second trifoliate leaves of To7G than in those of To7B. Hydrogen peroxide accumulation and lipid peroxidation were enhanced by chilling in To7G. Chilling-induced enhancement of antioxidant activity was more prominent in To7B than in To7G. High performance liquid chromatography analysis indicated that the contents of quercetin glycosides and isorhamnetin glycosides (3′,4′-dihydroxylated flavonol derivatives) increase in the second trifoliate leaves of To7B after chilling treatment, whereas the same treatment increased kaempferol glycoside (4′-monohydroxylated flavonol derivatives) content in the corresponding leaves of To7G. Histochemical staining also demonstrated chilling-induced flavonoid accumulation. Microarray analysis and real-time reverse transcription-PCR demonstrated that the transcript levels of soybean F3′H are upregulated by chilling. The differences in chilling injury, antioxidant activity and flavonoid species between the two NILs support the notion that soybean F3′H affects chilling tolerance by increasing antioxidant activity via production of 3′,4′-dihydroxylated flavonol derivatives. |
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Merr.] produced in cool climates. We previously isolated a soybean flavonoid 3′ hydroxylase (F3′H) gene corresponding to the T locus, which controls pubescence and seed coat color. A genetic link between the T gene and chilling tolerance has been reported, although the exact underlying mechanisms remain unclear. Using the soybean near-isogenic lines (NILs) To7B (TT) and To7G (tt), we examined the relationship between chilling injury, antioxidant activity and flavonoid profiles associated with chilling treatment (15°C). Chilling injury was more severe in the second trifoliate leaves of To7G than in those of To7B. Hydrogen peroxide accumulation and lipid peroxidation were enhanced by chilling in To7G. Chilling-induced enhancement of antioxidant activity was more prominent in To7B than in To7G. High performance liquid chromatography analysis indicated that the contents of quercetin glycosides and isorhamnetin glycosides (3′,4′-dihydroxylated flavonol derivatives) increase in the second trifoliate leaves of To7B after chilling treatment, whereas the same treatment increased kaempferol glycoside (4′-monohydroxylated flavonol derivatives) content in the corresponding leaves of To7G. Histochemical staining also demonstrated chilling-induced flavonoid accumulation. Microarray analysis and real-time reverse transcription-PCR demonstrated that the transcript levels of soybean F3′H are upregulated by chilling. The differences in chilling injury, antioxidant activity and flavonoid species between the two NILs support the notion that soybean F3′H affects chilling tolerance by increasing antioxidant activity via production of 3′,4′-dihydroxylated flavonol derivatives.</description><identifier>ISSN: 0918-9440</identifier><identifier>EISSN: 1618-0860</identifier><identifier>DOI: 10.1007/s10265-010-0345-2</identifier><identifier>PMID: 20428921</identifier><language>eng</language><publisher>Japan: Japan : Springer Japan</publisher><subject>Abiotic stress ; Adaptation, Physiological - genetics ; antioxidant activity ; Antioxidants ; Antioxidants - metabolism ; Biomedical and Life Sciences ; Chilling ; Chilling tolerance ; Chromatography, High Pressure Liquid ; Climate ; Cold ; Cold Temperature ; color ; DNA microarrays ; Flavonoid ; Flavonoids ; Flavonoids - biosynthesis ; Flavonoids - metabolism ; Flavonols ; Gene Expression Regulation, Plant ; genes ; Genes, Plant - genetics ; Glycine max ; Glycine max (L.) Merr ; Glycine max - cytology ; Glycine max - genetics ; Glycine max - metabolism ; glycosides ; High-performance liquid chromatography ; Hydrogen peroxide ; Hydrogen Peroxide - metabolism ; Hydroxylase ; Injuries ; isorhamnetin ; Kaempferol ; Leaves ; Life Sciences ; Lipid peroxidation ; Liquid chromatography ; loci ; microarray technology ; Oxidative Stress - genetics ; Peroxidation ; Phytochemicals ; Pigmentation - genetics ; Plant Biochemistry ; Plant biology ; Plant Ecology ; Plant Extracts - metabolism ; Plant Leaves - genetics ; Plant Leaves - metabolism ; Plant Physiology ; Plant Sciences ; Quercetin ; Regular Paper ; reverse transcriptase polymerase chain reaction ; seed coat ; Seeds ; Soybeans ; Thiobarbituric Acid Reactive Substances - metabolism ; Time Factors ; Transcription</subject><ispartof>Journal of plant research, 2011-01, Vol.124 (1), p.173-182</ispartof><rights>The Botanical Society of Japan and Springer 2010</rights><rights>The Botanical Society of Japan and Springer 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-8823300a236e40f455f8f54ba68225661a1325f65992efbf7666c09887f258013</citedby><cites>FETCH-LOGICAL-c551t-8823300a236e40f455f8f54ba68225661a1325f65992efbf7666c09887f258013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20428921$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Toda, Kyoko</creatorcontrib><creatorcontrib>Takahashi, Ryoji</creatorcontrib><creatorcontrib>Iwashina, Tsukasa</creatorcontrib><creatorcontrib>Hajika, Makita</creatorcontrib><title>Difference in chilling-induced flavonoid profiles, antioxidant activity and chilling tolerance between soybean near-isogenic lines for the pubescence color gene</title><title>Journal of plant research</title><addtitle>J Plant Res</addtitle><addtitle>J Plant Res</addtitle><description>Chilling tolerance is an important trait of soybeans [Glycine max (L.) Merr.] produced in cool climates. We previously isolated a soybean flavonoid 3′ hydroxylase (F3′H) gene corresponding to the T locus, which controls pubescence and seed coat color. A genetic link between the T gene and chilling tolerance has been reported, although the exact underlying mechanisms remain unclear. Using the soybean near-isogenic lines (NILs) To7B (TT) and To7G (tt), we examined the relationship between chilling injury, antioxidant activity and flavonoid profiles associated with chilling treatment (15°C). Chilling injury was more severe in the second trifoliate leaves of To7G than in those of To7B. Hydrogen peroxide accumulation and lipid peroxidation were enhanced by chilling in To7G. Chilling-induced enhancement of antioxidant activity was more prominent in To7B than in To7G. High performance liquid chromatography analysis indicated that the contents of quercetin glycosides and isorhamnetin glycosides (3′,4′-dihydroxylated flavonol derivatives) increase in the second trifoliate leaves of To7B after chilling treatment, whereas the same treatment increased kaempferol glycoside (4′-monohydroxylated flavonol derivatives) content in the corresponding leaves of To7G. Histochemical staining also demonstrated chilling-induced flavonoid accumulation. Microarray analysis and real-time reverse transcription-PCR demonstrated that the transcript levels of soybean F3′H are upregulated by chilling. The differences in chilling injury, antioxidant activity and flavonoid species between the two NILs support the notion that soybean F3′H affects chilling tolerance by increasing antioxidant activity via production of 3′,4′-dihydroxylated flavonol derivatives.</description><subject>Abiotic stress</subject><subject>Adaptation, Physiological - genetics</subject><subject>antioxidant activity</subject><subject>Antioxidants</subject><subject>Antioxidants - metabolism</subject><subject>Biomedical and Life Sciences</subject><subject>Chilling</subject><subject>Chilling tolerance</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Climate</subject><subject>Cold</subject><subject>Cold Temperature</subject><subject>color</subject><subject>DNA microarrays</subject><subject>Flavonoid</subject><subject>Flavonoids</subject><subject>Flavonoids - biosynthesis</subject><subject>Flavonoids - metabolism</subject><subject>Flavonols</subject><subject>Gene Expression Regulation, Plant</subject><subject>genes</subject><subject>Genes, Plant - genetics</subject><subject>Glycine max</subject><subject>Glycine max (L.) Merr</subject><subject>Glycine max - cytology</subject><subject>Glycine max - genetics</subject><subject>Glycine max - metabolism</subject><subject>glycosides</subject><subject>High-performance liquid chromatography</subject><subject>Hydrogen peroxide</subject><subject>Hydrogen Peroxide - metabolism</subject><subject>Hydroxylase</subject><subject>Injuries</subject><subject>isorhamnetin</subject><subject>Kaempferol</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Lipid peroxidation</subject><subject>Liquid chromatography</subject><subject>loci</subject><subject>microarray technology</subject><subject>Oxidative Stress - genetics</subject><subject>Peroxidation</subject><subject>Phytochemicals</subject><subject>Pigmentation - genetics</subject><subject>Plant Biochemistry</subject><subject>Plant biology</subject><subject>Plant Ecology</subject><subject>Plant Extracts - metabolism</subject><subject>Plant Leaves - genetics</subject><subject>Plant Leaves - metabolism</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Quercetin</subject><subject>Regular Paper</subject><subject>reverse transcriptase polymerase chain reaction</subject><subject>seed coat</subject><subject>Seeds</subject><subject>Soybeans</subject><subject>Thiobarbituric Acid Reactive Substances - metabolism</subject><subject>Time Factors</subject><subject>Transcription</subject><issn>0918-9440</issn><issn>1618-0860</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kc9u1DAQxi0EokvhAbiAxaUcCIwd27GPqOWfVIkD9Gw5yXjrKmsvdlLYt-FR8XZLkTjUl7HGv_lmxh8hzxm8ZQDdu8KAK9kAgwZaIRv-gKyYYroBreAhWYGpdyMEHJEnpVwBsE4a_ZgccRBcG85W5PdZ8B4zxgFpiHS4DNMU4roJcVwGHKmf3HWKKYx0m5MPE5Y31MU5pF9hrJG6YQ7XYd7V5HhXTec0YXZ7zR7nn4iRlrTr0UUa0eUmlLTGGAZaYSzUp0znS6Tbpccy3IwypKkmK4RPySPvpoLPbuMxufj44fvp5-b866cvp-_Pm0FKNjda87YFcLxVKMALKb32UvROac6lUsyxlkuvpDEcfe87pdQARuvOc6mBtcfk5KBb9_yxYJntJtRhpslFTEuxRmmmuJC8kq_vJVsQIFqjASr66j_0Ki051j2sZrrTYG4gdoCGnErJ6O02h43LO8vA7n22B59t9dnufbb7GV7cCi_9Bse7ir_GVoAfgFKf4hrzv873qb48FHmXrFvnUOzFN14_B5jh9cj2D5PfvOI</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Toda, Kyoko</creator><creator>Takahashi, Ryoji</creator><creator>Iwashina, Tsukasa</creator><creator>Hajika, Makita</creator><general>Japan : Springer Japan</general><general>Springer Japan</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7ST</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>SOI</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20110101</creationdate><title>Difference in chilling-induced flavonoid profiles, antioxidant activity and chilling tolerance between soybean near-isogenic lines for the pubescence color gene</title><author>Toda, Kyoko ; Takahashi, Ryoji ; Iwashina, Tsukasa ; Hajika, Makita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c551t-8823300a236e40f455f8f54ba68225661a1325f65992efbf7666c09887f258013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Abiotic stress</topic><topic>Adaptation, Physiological - genetics</topic><topic>antioxidant activity</topic><topic>Antioxidants</topic><topic>Antioxidants - metabolism</topic><topic>Biomedical and Life Sciences</topic><topic>Chilling</topic><topic>Chilling tolerance</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Climate</topic><topic>Cold</topic><topic>Cold Temperature</topic><topic>color</topic><topic>DNA microarrays</topic><topic>Flavonoid</topic><topic>Flavonoids</topic><topic>Flavonoids - biosynthesis</topic><topic>Flavonoids - metabolism</topic><topic>Flavonols</topic><topic>Gene Expression Regulation, Plant</topic><topic>genes</topic><topic>Genes, Plant - genetics</topic><topic>Glycine max</topic><topic>Glycine max (L.) Merr</topic><topic>Glycine max - cytology</topic><topic>Glycine max - genetics</topic><topic>Glycine max - metabolism</topic><topic>glycosides</topic><topic>High-performance liquid chromatography</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen Peroxide - metabolism</topic><topic>Hydroxylase</topic><topic>Injuries</topic><topic>isorhamnetin</topic><topic>Kaempferol</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Lipid peroxidation</topic><topic>Liquid chromatography</topic><topic>loci</topic><topic>microarray technology</topic><topic>Oxidative Stress - genetics</topic><topic>Peroxidation</topic><topic>Phytochemicals</topic><topic>Pigmentation - genetics</topic><topic>Plant Biochemistry</topic><topic>Plant biology</topic><topic>Plant Ecology</topic><topic>Plant Extracts - metabolism</topic><topic>Plant Leaves - genetics</topic><topic>Plant Leaves - metabolism</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Quercetin</topic><topic>Regular Paper</topic><topic>reverse transcriptase polymerase chain reaction</topic><topic>seed coat</topic><topic>Seeds</topic><topic>Soybeans</topic><topic>Thiobarbituric Acid Reactive Substances - metabolism</topic><topic>Time Factors</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Toda, Kyoko</creatorcontrib><creatorcontrib>Takahashi, Ryoji</creatorcontrib><creatorcontrib>Iwashina, Tsukasa</creatorcontrib><creatorcontrib>Hajika, Makita</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Journal of plant research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Toda, Kyoko</au><au>Takahashi, Ryoji</au><au>Iwashina, Tsukasa</au><au>Hajika, Makita</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Difference in chilling-induced flavonoid profiles, antioxidant activity and chilling tolerance between soybean near-isogenic lines for the pubescence color gene</atitle><jtitle>Journal of plant research</jtitle><stitle>J Plant Res</stitle><addtitle>J Plant Res</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>124</volume><issue>1</issue><spage>173</spage><epage>182</epage><pages>173-182</pages><issn>0918-9440</issn><eissn>1618-0860</eissn><abstract>Chilling tolerance is an important trait of soybeans [Glycine max (L.) Merr.] produced in cool climates. We previously isolated a soybean flavonoid 3′ hydroxylase (F3′H) gene corresponding to the T locus, which controls pubescence and seed coat color. A genetic link between the T gene and chilling tolerance has been reported, although the exact underlying mechanisms remain unclear. Using the soybean near-isogenic lines (NILs) To7B (TT) and To7G (tt), we examined the relationship between chilling injury, antioxidant activity and flavonoid profiles associated with chilling treatment (15°C). Chilling injury was more severe in the second trifoliate leaves of To7G than in those of To7B. Hydrogen peroxide accumulation and lipid peroxidation were enhanced by chilling in To7G. Chilling-induced enhancement of antioxidant activity was more prominent in To7B than in To7G. High performance liquid chromatography analysis indicated that the contents of quercetin glycosides and isorhamnetin glycosides (3′,4′-dihydroxylated flavonol derivatives) increase in the second trifoliate leaves of To7B after chilling treatment, whereas the same treatment increased kaempferol glycoside (4′-monohydroxylated flavonol derivatives) content in the corresponding leaves of To7G. Histochemical staining also demonstrated chilling-induced flavonoid accumulation. Microarray analysis and real-time reverse transcription-PCR demonstrated that the transcript levels of soybean F3′H are upregulated by chilling. The differences in chilling injury, antioxidant activity and flavonoid species between the two NILs support the notion that soybean F3′H affects chilling tolerance by increasing antioxidant activity via production of 3′,4′-dihydroxylated flavonol derivatives.</abstract><cop>Japan</cop><pub>Japan : Springer Japan</pub><pmid>20428921</pmid><doi>10.1007/s10265-010-0345-2</doi><tpages>10</tpages></addata></record> |
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subjects | Abiotic stress Adaptation, Physiological - genetics antioxidant activity Antioxidants Antioxidants - metabolism Biomedical and Life Sciences Chilling Chilling tolerance Chromatography, High Pressure Liquid Climate Cold Cold Temperature color DNA microarrays Flavonoid Flavonoids Flavonoids - biosynthesis Flavonoids - metabolism Flavonols Gene Expression Regulation, Plant genes Genes, Plant - genetics Glycine max Glycine max (L.) Merr Glycine max - cytology Glycine max - genetics Glycine max - metabolism glycosides High-performance liquid chromatography Hydrogen peroxide Hydrogen Peroxide - metabolism Hydroxylase Injuries isorhamnetin Kaempferol Leaves Life Sciences Lipid peroxidation Liquid chromatography loci microarray technology Oxidative Stress - genetics Peroxidation Phytochemicals Pigmentation - genetics Plant Biochemistry Plant biology Plant Ecology Plant Extracts - metabolism Plant Leaves - genetics Plant Leaves - metabolism Plant Physiology Plant Sciences Quercetin Regular Paper reverse transcriptase polymerase chain reaction seed coat Seeds Soybeans Thiobarbituric Acid Reactive Substances - metabolism Time Factors Transcription |
title | Difference in chilling-induced flavonoid profiles, antioxidant activity and chilling tolerance between soybean near-isogenic lines for the pubescence color gene |
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