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Overexpression of a Cinnamyl Alcohol Dehydrogenase-Coding Gene, GsCAD1 , from Wild Soybean Enhances Resistance to Soybean Mosaic Virus
Soybean mosaic virus (SMV) is the most prevalent soybean viral disease in the world. As a critical enzyme in the secondary metabolism of plants, especially in lignin synthesis, cinnamyl alcohol dehydrogenase (CAD) is widely involved in plant growth and development, and in defense against pathogen in...
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Published in: | International journal of molecular sciences 2022-12, Vol.23 (23), p.15206 |
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description | Soybean mosaic virus (SMV) is the most prevalent soybean viral disease in the world. As a critical enzyme in the secondary metabolism of plants, especially in lignin synthesis, cinnamyl alcohol dehydrogenase (CAD) is widely involved in plant growth and development, and in defense against pathogen infestation. Here, we performed RNAseq-based transcriptome analyses of a highly SMV-resistant accession (BYO-15) of wild soybean (
) and a SMV-susceptible soybean cultivar (Williams 82), also sequenced together with a resistant plant and a susceptible plant of their hybrid descendants at the F3 generation at 7 and 14 days post-inoculation with SMV. We found that the expression of
(from
) was significantly up-regulated in the wild soybean and the resistant F3 plant, while the
from the cultivated soybean (
) did not show a significant and persistent induction in the soybean cultivar and the susceptible F3 plant, suggesting that
might play an important role in SMV resistance. We cloned
and overexpressed it in the SMV-susceptible cultivar Williams 82, and we found that two independent
-overexpression (OE) lines showed significantly enhanced SMV resistance compared with the non-transformed wild-type (WT) control. Intriguingly, the lignin contents in both OE lines were higher than the WT control. Further liquid chromatography (HPLC) analysis showed that the contents of salicylic acid (SA) were significantly more improved in the OE lines than that of the wild-type (WT), coinciding with the up-regulated expression of an SA marker gene. Finally, we observed that
-overexpression affected the accumulation of SMV in leaves. Collectively, our results suggest that
enhances resistance to SMV in soybeans, most likely by affecting the contents of lignin and SA. |
doi_str_mv | 10.3390/ijms232315206 |
format | article |
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) and a SMV-susceptible soybean cultivar (Williams 82), also sequenced together with a resistant plant and a susceptible plant of their hybrid descendants at the F3 generation at 7 and 14 days post-inoculation with SMV. We found that the expression of
(from
) was significantly up-regulated in the wild soybean and the resistant F3 plant, while the
from the cultivated soybean (
) did not show a significant and persistent induction in the soybean cultivar and the susceptible F3 plant, suggesting that
might play an important role in SMV resistance. We cloned
and overexpressed it in the SMV-susceptible cultivar Williams 82, and we found that two independent
-overexpression (OE) lines showed significantly enhanced SMV resistance compared with the non-transformed wild-type (WT) control. Intriguingly, the lignin contents in both OE lines were higher than the WT control. Further liquid chromatography (HPLC) analysis showed that the contents of salicylic acid (SA) were significantly more improved in the OE lines than that of the wild-type (WT), coinciding with the up-regulated expression of an SA marker gene. Finally, we observed that
-overexpression affected the accumulation of SMV in leaves. Collectively, our results suggest that
enhances resistance to SMV in soybeans, most likely by affecting the contents of lignin and SA.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms232315206</identifier><identifier>PMID: 36499529</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Alcohol ; Alcohol dehydrogenase ; Biosynthesis ; Cinnamyl-alcohol dehydrogenase ; Cloning ; Cultivars ; Dehydrogenases ; Disease resistance ; Disease Resistance - genetics ; Enzymes ; Gene expression ; Genetic diversity ; Glycine ; Glycine max - genetics ; Glycine soja ; GsCAD1 ; High performance liquid chromatography ; Inoculation ; Lignin ; Liquid chromatography ; Mutation ; Pathogens ; Plant Diseases - genetics ; Plant growth ; Plant resistance ; Polymerization ; Potyvirus ; Proteins ; Salicylic Acid ; Signal transduction ; soybean mosaic virus ; Soybeans ; Transcriptomes ; Transgenic plants ; wild soybean</subject><ispartof>International journal of molecular sciences, 2022-12, Vol.23 (23), p.15206</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-615fa671c26a6b8d801ac29006431546a033a6bc60115efe6924c4ee63b8c5703</citedby><cites>FETCH-LOGICAL-c481t-615fa671c26a6b8d801ac29006431546a033a6bc60115efe6924c4ee63b8c5703</cites><orcidid>0000-0001-7619-2385 ; 0000-0003-2409-2299 ; 0000-0001-5481-1675</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2748550230/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2748550230?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36499529$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xun, Hongwei</creatorcontrib><creatorcontrib>Qian, Xueyan</creatorcontrib><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Yu, Jiaxin</creatorcontrib><creatorcontrib>Zhang, Xue</creatorcontrib><creatorcontrib>Pang, Jinsong</creatorcontrib><creatorcontrib>Wang, Shucai</creatorcontrib><creatorcontrib>Jiang, Lili</creatorcontrib><creatorcontrib>Dong, Yingshan</creatorcontrib><creatorcontrib>Liu, Bao</creatorcontrib><title>Overexpression of a Cinnamyl Alcohol Dehydrogenase-Coding Gene, GsCAD1 , from Wild Soybean Enhances Resistance to Soybean Mosaic Virus</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Soybean mosaic virus (SMV) is the most prevalent soybean viral disease in the world. As a critical enzyme in the secondary metabolism of plants, especially in lignin synthesis, cinnamyl alcohol dehydrogenase (CAD) is widely involved in plant growth and development, and in defense against pathogen infestation. Here, we performed RNAseq-based transcriptome analyses of a highly SMV-resistant accession (BYO-15) of wild soybean (
) and a SMV-susceptible soybean cultivar (Williams 82), also sequenced together with a resistant plant and a susceptible plant of their hybrid descendants at the F3 generation at 7 and 14 days post-inoculation with SMV. We found that the expression of
(from
) was significantly up-regulated in the wild soybean and the resistant F3 plant, while the
from the cultivated soybean (
) did not show a significant and persistent induction in the soybean cultivar and the susceptible F3 plant, suggesting that
might play an important role in SMV resistance. We cloned
and overexpressed it in the SMV-susceptible cultivar Williams 82, and we found that two independent
-overexpression (OE) lines showed significantly enhanced SMV resistance compared with the non-transformed wild-type (WT) control. Intriguingly, the lignin contents in both OE lines were higher than the WT control. Further liquid chromatography (HPLC) analysis showed that the contents of salicylic acid (SA) were significantly more improved in the OE lines than that of the wild-type (WT), coinciding with the up-regulated expression of an SA marker gene. Finally, we observed that
-overexpression affected the accumulation of SMV in leaves. Collectively, our results suggest that
enhances resistance to SMV in soybeans, most likely by affecting the contents of lignin and SA.</description><subject>Alcohol</subject><subject>Alcohol dehydrogenase</subject><subject>Biosynthesis</subject><subject>Cinnamyl-alcohol dehydrogenase</subject><subject>Cloning</subject><subject>Cultivars</subject><subject>Dehydrogenases</subject><subject>Disease resistance</subject><subject>Disease Resistance - genetics</subject><subject>Enzymes</subject><subject>Gene expression</subject><subject>Genetic diversity</subject><subject>Glycine</subject><subject>Glycine max - genetics</subject><subject>Glycine soja</subject><subject>GsCAD1</subject><subject>High performance liquid chromatography</subject><subject>Inoculation</subject><subject>Lignin</subject><subject>Liquid chromatography</subject><subject>Mutation</subject><subject>Pathogens</subject><subject>Plant Diseases - genetics</subject><subject>Plant growth</subject><subject>Plant resistance</subject><subject>Polymerization</subject><subject>Potyvirus</subject><subject>Proteins</subject><subject>Salicylic Acid</subject><subject>Signal transduction</subject><subject>soybean mosaic virus</subject><subject>Soybeans</subject><subject>Transcriptomes</subject><subject>Transgenic plants</subject><subject>wild soybean</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkktvEzEQgFcIREvhyBVZ4sKhC36td31BitISKhVV4nm0Zr2ziaNdO9ibivwBfjcOKVHLySPPp0_zKoqXjL4VQtN3bj0mLrhgFafqUXHKJOclpap-fC8-KZ6ltKY0g5V-WpwIJbWuuD4tft_cYsRfm4gpueBJ6AmQufMext1AZoMNqzCQC1ztuhiW6CFhOQ-d80uyQI_nZJHmswtGzkkfw0h-uKEjX8KuRfDk0q_AW0zkMyaXpn1MpnBMfwoJnCXfXdym58WTHoaEL-7es-Lbh8uv84_l9c3iaj67Lq1s2FQqVvWgama5AtU2XUMZWK5zizIPQCqgQuSEVZSxCntUmksrEZVoG1vVVJwVVwdvF2BtNtGNEHcmgDN_P0JcGoiTswMawBabWjU2W6WWGmSbTRwVSugF7F3vD67Nth2xs-inCMMD6cOMdyuzDLdG15KySmXBmztBDD-3mCYzumRxGMBj2CbD60oIqlmtM_r6P3QdttHnUWVKNlWVV7uvqDxQNoaUIvbHYhg1-2sxD64l86_ud3Ck_52H-APQcLss</recordid><startdate>20221202</startdate><enddate>20221202</enddate><creator>Xun, Hongwei</creator><creator>Qian, Xueyan</creator><creator>Wang, Meng</creator><creator>Yu, Jiaxin</creator><creator>Zhang, Xue</creator><creator>Pang, Jinsong</creator><creator>Wang, Shucai</creator><creator>Jiang, Lili</creator><creator>Dong, Yingshan</creator><creator>Liu, Bao</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7619-2385</orcidid><orcidid>https://orcid.org/0000-0003-2409-2299</orcidid><orcidid>https://orcid.org/0000-0001-5481-1675</orcidid></search><sort><creationdate>20221202</creationdate><title>Overexpression of a Cinnamyl Alcohol Dehydrogenase-Coding Gene, GsCAD1 , from Wild Soybean Enhances Resistance to Soybean Mosaic Virus</title><author>Xun, Hongwei ; Qian, Xueyan ; Wang, Meng ; Yu, Jiaxin ; Zhang, Xue ; Pang, Jinsong ; Wang, Shucai ; Jiang, Lili ; Dong, Yingshan ; Liu, Bao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-615fa671c26a6b8d801ac29006431546a033a6bc60115efe6924c4ee63b8c5703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alcohol</topic><topic>Alcohol dehydrogenase</topic><topic>Biosynthesis</topic><topic>Cinnamyl-alcohol dehydrogenase</topic><topic>Cloning</topic><topic>Cultivars</topic><topic>Dehydrogenases</topic><topic>Disease resistance</topic><topic>Disease Resistance - genetics</topic><topic>Enzymes</topic><topic>Gene expression</topic><topic>Genetic diversity</topic><topic>Glycine</topic><topic>Glycine max - genetics</topic><topic>Glycine soja</topic><topic>GsCAD1</topic><topic>High performance liquid chromatography</topic><topic>Inoculation</topic><topic>Lignin</topic><topic>Liquid chromatography</topic><topic>Mutation</topic><topic>Pathogens</topic><topic>Plant Diseases - genetics</topic><topic>Plant growth</topic><topic>Plant resistance</topic><topic>Polymerization</topic><topic>Potyvirus</topic><topic>Proteins</topic><topic>Salicylic Acid</topic><topic>Signal transduction</topic><topic>soybean mosaic virus</topic><topic>Soybeans</topic><topic>Transcriptomes</topic><topic>Transgenic plants</topic><topic>wild soybean</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xun, Hongwei</creatorcontrib><creatorcontrib>Qian, Xueyan</creatorcontrib><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Yu, Jiaxin</creatorcontrib><creatorcontrib>Zhang, Xue</creatorcontrib><creatorcontrib>Pang, Jinsong</creatorcontrib><creatorcontrib>Wang, Shucai</creatorcontrib><creatorcontrib>Jiang, Lili</creatorcontrib><creatorcontrib>Dong, Yingshan</creatorcontrib><creatorcontrib>Liu, Bao</creatorcontrib><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep (ProQuest)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content 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 China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals(OpenAccess)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xun, Hongwei</au><au>Qian, Xueyan</au><au>Wang, Meng</au><au>Yu, Jiaxin</au><au>Zhang, Xue</au><au>Pang, Jinsong</au><au>Wang, Shucai</au><au>Jiang, Lili</au><au>Dong, Yingshan</au><au>Liu, Bao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Overexpression of a Cinnamyl Alcohol Dehydrogenase-Coding Gene, GsCAD1 , from Wild Soybean Enhances Resistance to Soybean Mosaic Virus</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2022-12-02</date><risdate>2022</risdate><volume>23</volume><issue>23</issue><spage>15206</spage><pages>15206-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Soybean mosaic virus (SMV) is the most prevalent soybean viral disease in the world. As a critical enzyme in the secondary metabolism of plants, especially in lignin synthesis, cinnamyl alcohol dehydrogenase (CAD) is widely involved in plant growth and development, and in defense against pathogen infestation. Here, we performed RNAseq-based transcriptome analyses of a highly SMV-resistant accession (BYO-15) of wild soybean (
) and a SMV-susceptible soybean cultivar (Williams 82), also sequenced together with a resistant plant and a susceptible plant of their hybrid descendants at the F3 generation at 7 and 14 days post-inoculation with SMV. We found that the expression of
(from
) was significantly up-regulated in the wild soybean and the resistant F3 plant, while the
from the cultivated soybean (
) did not show a significant and persistent induction in the soybean cultivar and the susceptible F3 plant, suggesting that
might play an important role in SMV resistance. We cloned
and overexpressed it in the SMV-susceptible cultivar Williams 82, and we found that two independent
-overexpression (OE) lines showed significantly enhanced SMV resistance compared with the non-transformed wild-type (WT) control. Intriguingly, the lignin contents in both OE lines were higher than the WT control. Further liquid chromatography (HPLC) analysis showed that the contents of salicylic acid (SA) were significantly more improved in the OE lines than that of the wild-type (WT), coinciding with the up-regulated expression of an SA marker gene. Finally, we observed that
-overexpression affected the accumulation of SMV in leaves. Collectively, our results suggest that
enhances resistance to SMV in soybeans, most likely by affecting the contents of lignin and SA.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36499529</pmid><doi>10.3390/ijms232315206</doi><orcidid>https://orcid.org/0000-0001-7619-2385</orcidid><orcidid>https://orcid.org/0000-0003-2409-2299</orcidid><orcidid>https://orcid.org/0000-0001-5481-1675</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alcohol Alcohol dehydrogenase Biosynthesis Cinnamyl-alcohol dehydrogenase Cloning Cultivars Dehydrogenases Disease resistance Disease Resistance - genetics Enzymes Gene expression Genetic diversity Glycine Glycine max - genetics Glycine soja GsCAD1 High performance liquid chromatography Inoculation Lignin Liquid chromatography Mutation Pathogens Plant Diseases - genetics Plant growth Plant resistance Polymerization Potyvirus Proteins Salicylic Acid Signal transduction soybean mosaic virus Soybeans Transcriptomes Transgenic plants wild soybean |
title | Overexpression of a Cinnamyl Alcohol Dehydrogenase-Coding Gene, GsCAD1 , from Wild Soybean Enhances Resistance to Soybean Mosaic Virus |
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