Overexpression of transcription factor SlWRKY28 improved the tolerance of Populus davidiana × P. bolleana to alkaline salt stress.
Identifieur interne : 000231 ( Main/Exploration ); précédent : 000230; suivant : 000232Overexpression of transcription factor SlWRKY28 improved the tolerance of Populus davidiana × P. bolleana to alkaline salt stress.
Auteurs : Xin Wang [République populaire de Chine] ; Zainab Ajab [République populaire de Chine] ; Chenxi Liu [République populaire de Chine] ; Songmiao Hu [République populaire de Chine] ; Jiali Liu [République populaire de Chine] ; Qingjie Guan [République populaire de Chine]Source :
- BMC genetics [ 1471-2156 ] ; 2020.
Abstract
BACKGROUND
WRKY transcription factors (TFs) have been suggested to play crucial roles in the response to biotic and abiotic stresses. This study is the first to report the alkaline salt regulation of the WRKY gene.
RESULTS
In this study, we cloned a WRKY gene (SlWRKY28) from the Salix linearistipularis and then transferred to the Populus davidiana × P. bolleana for expression. Sequence analysis on the transcriptome of Salix linearistipular showed the significant up-regulation of WRKY gene expression in response to salt-alkali stress in seedlings. Our data showed that SlWRKY28 localized to the nucleus. Furthermore, the expression of the SlWRKY28 from female plants increased with saline-alkali stress according to the northern blot analysis results. The results of 3,3'-Diaminobenzidine (DAB) staining showed that hydrogen peroxide (H
CONCLUSIONS
We found out the SlWRKY28 induced regulation of the enzyme gene in the reactive oxygen species (ROS) scavenging pathway is a potential mechanism for transgenic lines to improve their resistance to alkaline salt. This study shows theoretical and practical significance in determining SlWRKY28 transcription factors involved in the regulation of alkaline salt tolerance.
DOI: 10.1186/s12863-020-00904-9
PubMed: 32928116
PubMed Central: PMC7488863
Affiliations:
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150040</wicri:regionArea><wicri:noRegion>150040</wicri:noRegion></affiliation></author><author><name sortKey="Ajab, Zainab" sort="Ajab, Zainab" uniqKey="Ajab Z" first="Zainab" last="Ajab">Zainab Ajab</name><affiliation wicri:level="1"><nlm:affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040</wicri:regionArea><wicri:noRegion>150040</wicri:noRegion></affiliation></author><author><name sortKey="Liu, Chenxi" sort="Liu, Chenxi" uniqKey="Liu C" first="Chenxi" last="Liu">Chenxi Liu</name><affiliation wicri:level="1"><nlm:affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040</wicri:regionArea><wicri:noRegion>150040</wicri:noRegion></affiliation></author><author><name sortKey="Hu, Songmiao" sort="Hu, Songmiao" uniqKey="Hu S" first="Songmiao" last="Hu">Songmiao Hu</name><affiliation wicri:level="1"><nlm:affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040</wicri:regionArea><wicri:noRegion>150040</wicri:noRegion></affiliation></author><author><name sortKey="Liu, Jiali" sort="Liu, Jiali" uniqKey="Liu J" first="Jiali" last="Liu">Jiali Liu</name><affiliation wicri:level="1"><nlm:affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040</wicri:regionArea><wicri:noRegion>150040</wicri:noRegion></affiliation></author><author><name sortKey="Guan, Qingjie" sort="Guan, Qingjie" uniqKey="Guan Q" first="Qingjie" last="Guan">Qingjie Guan</name><affiliation wicri:level="1"><nlm:affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China. guanqingjie@nefu.edu.cn.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040</wicri:regionArea><wicri:noRegion>150040</wicri:noRegion></affiliation></author></analytic><series><title level="j">BMC genetics</title><idno type="eISSN">1471-2156</idno><imprint><date when="2020" type="published">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p><b>BACKGROUND</b></p><p>WRKY transcription factors (TFs) have been suggested to play crucial roles in the response to biotic and abiotic stresses. This study is the first to report the alkaline salt regulation of the WRKY gene.</p></div><div type="abstract" xml:lang="en"><p><b>RESULTS</b></p><p>In this study, we cloned a WRKY gene (SlWRKY28) from the Salix linearistipularis and then transferred to the Populus davidiana × P. bolleana for expression. Sequence analysis on the transcriptome of Salix linearistipular showed the significant up-regulation of WRKY gene expression in response to salt-alkali stress in seedlings. Our data showed that SlWRKY28 localized to the nucleus. Furthermore, the expression of the SlWRKY28 from female plants increased with saline-alkali stress according to the northern blot analysis results. The results of 3,3'-Diaminobenzidine (DAB) staining showed that hydrogen peroxide (H</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSIONS</b></p><p>We found out the SlWRKY28 induced regulation of the enzyme gene in the reactive oxygen species (ROS) scavenging pathway is a potential mechanism for transgenic lines to improve their resistance to alkaline salt. This study shows theoretical and practical significance in determining SlWRKY28 transcription factors involved in the regulation of alkaline salt tolerance.</p></div></front></TEI><pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">32928116</PMID><DateRevised><Year>2020</Year><Month>11</Month><Day>04</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1471-2156</ISSN><JournalIssue CitedMedium="Internet"><Volume>21</Volume><Issue>1</Issue><PubDate><Year>2020</Year><Month>09</Month><Day>14</Day></PubDate></JournalIssue><Title>BMC genetics</Title><ISOAbbreviation>BMC Genet</ISOAbbreviation></Journal><ArticleTitle>Overexpression of transcription factor SlWRKY28 improved the tolerance of Populus davidiana × P. bolleana to alkaline salt stress.</ArticleTitle><Pagination><MedlinePgn>103</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1186/s12863-020-00904-9</ELocationID><Abstract><AbstractText Label="BACKGROUND">WRKY transcription factors (TFs) have been suggested to play crucial roles in the response to biotic and abiotic stresses. This study is the first to report the alkaline salt regulation of the WRKY gene.</AbstractText><AbstractText Label="RESULTS">In this study, we cloned a WRKY gene (SlWRKY28) from the Salix linearistipularis and then transferred to the Populus davidiana × P. bolleana for expression. Sequence analysis on the transcriptome of Salix linearistipular showed the significant up-regulation of WRKY gene expression in response to salt-alkali stress in seedlings. Our data showed that SlWRKY28 localized to the nucleus. Furthermore, the expression of the SlWRKY28 from female plants increased with saline-alkali stress according to the northern blot analysis results. The results of 3,3'-Diaminobenzidine (DAB) staining showed that hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) concentration was lower under stress, but ascorbate peroxidase (APX) enzyme activity was significantly higher in the overexpressed plants than that in non-transgenic (NT) plants.</AbstractText><AbstractText Label="CONCLUSIONS">We found out the SlWRKY28 induced regulation of the enzyme gene in the reactive oxygen species (ROS) scavenging pathway is a potential mechanism for transgenic lines to improve their resistance to alkaline salt. This study shows theoretical and practical significance in determining SlWRKY28 transcription factors involved in the regulation of alkaline salt tolerance.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Xin</ForeName><Initials>X</Initials><AffiliationInfo><Affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ajab</LastName><ForeName>Zainab</ForeName><Initials>Z</Initials><AffiliationInfo><Affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Liu</LastName><ForeName>Chenxi</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Hu</LastName><ForeName>Songmiao</ForeName><Initials>S</Initials><AffiliationInfo><Affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Liu</LastName><ForeName>Jiali</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Guan</LastName><ForeName>Qingjie</ForeName><Initials>Q</Initials><Identifier Source="ORCID">0000-0002-9438-1427</Identifier><AffiliationInfo><Affiliation>Key Laboratory of Saline-alkali Vegetation Ecology Restoration, Northeast Forestry University, Harbin, 150040, China. guanqingjie@nefu.edu.cn.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2020</Year><Month>09</Month><Day>14</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>BMC Genet</MedlineTA><NlmUniqueID>100966978</NlmUniqueID><ISSNLinking>1471-2156</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Adversity stress</Keyword><Keyword MajorTopicYN="Y">Populus davidiana × P. bolleana</Keyword><Keyword MajorTopicYN="Y">Salix linearistipularis</Keyword><Keyword MajorTopicYN="Y">SlWRKY28</Keyword><Keyword MajorTopicYN="Y">Transgenesis</Keyword><Keyword MajorTopicYN="Y">WRKY transcription 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Hu</name><name sortKey="Liu, Chenxi" sort="Liu, Chenxi" uniqKey="Liu C" first="Chenxi" last="Liu">Chenxi Liu</name><name sortKey="Liu, Jiali" sort="Liu, Jiali" uniqKey="Liu J" first="Jiali" last="Liu">Jiali Liu</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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