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Overexpression of phosphatidylserine synthase IbPSS1 affords cellular Na+ homeostasis and salt tolerance by activating plasma membrane Na+/H+ antiport activity in sweet potato roots.

Identifieur interne : 000030 ( Main/Exploration ); précédent : 000029; suivant : 000031

Overexpression of phosphatidylserine synthase IbPSS1 affords cellular Na+ homeostasis and salt tolerance by activating plasma membrane Na+/H+ antiport activity in sweet potato roots.

Auteurs : Yicheng Yu ; Ying Xuan ; Xiaofeng Bian [République populaire de Chine] ; Lei Zhang ; Zhiyuan Pan ; Meng Kou ; Qinghe Cao ; Zhonghou Tang ; Qiang Li ; Daifu Ma ; Zongyun Li ; Jian Sun

Source :

RBID : pubmed:32821414

Abstract

Phosphatidylserine synthase (PSS)-mediated phosphatidylserine (PS) synthesis is crucial for plant development. However, little is known about the contribution of PSS to Na+ homeostasis regulation and salt tolerance in plants. Here, we cloned the IbPSS1 gene, which encodes an ortholog of Arabidopsis AtPSS1, from sweet potato (Ipomoea batatas (L.) Lam.). The transient expression of IbPSS1 in Nicotiana benthamiana leaves increased PS abundance. We then established an efficient Agrobacterium rhizogenes-mediated in vivo root transgenic system for sweet potato. Overexpression of IbPSS1 through this system markedly decreased cellular Na+ accumulation in salinized transgenic roots (TRs) compared with adventitious roots. The overexpression of IbPSS1 enhanced salt-induced Na+/H+ antiport activity and increased plasma membrane (PM) Ca2+-permeable channel sensitivity to NaCl and H2O2 in the TRs. We confirmed the important role of IbPSS1 in improving salt tolerance in transgenic sweet potato lines obtained from an Agrobacterium tumefaciens-mediated transformation system. Similarly, compared with the wild-type (WT) plants, the transgenic lines presented decreased Na+ accumulation, enhanced Na+ exclusion, and increased PM Ca2+-permeable channel sensitivity to NaCl and H2O2 in the roots. Exogenous application of lysophosphatidylserine triggered similar shifts in Na+ accumulation and Na+ and Ca2+ fluxes in the salinized roots of WT. Overall, this study provides an efficient and reliable transgenic method for functional genomic studies of sweet potato. Our results revealed that IbPSS1 contributes to the salt tolerance of sweet potato by enabling Na+ homeostasis and Na+ exclusion in the roots, and the latter process is possibly controlled by PS reinforcing Ca2+ signaling in the roots.

DOI: 10.1038/s41438-020-00358-1
PubMed: 32821414
PubMed Central: PMC7395154


Affiliations:


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affords cellular Na
<sup>+</sup>
homeostasis and salt tolerance by activating plasma membrane Na
<sup>+</sup>
/H
<sup>+</sup>
antiport activity in sweet potato roots.</title>
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<title xml:lang="en">Overexpression of phosphatidylserine synthase
<i>IbPSS1</i>
affords cellular Na
<sup>+</sup>
homeostasis and salt tolerance by activating plasma membrane Na
<sup>+</sup>
/H
<sup>+</sup>
antiport activity in sweet potato roots.</title>
<author>
<name sortKey="Yu, Yicheng" sort="Yu, Yicheng" uniqKey="Yu Y" first="Yicheng" last="Yu">Yicheng Yu</name>
<affiliation>
<nlm:affiliation>Jiangsu Key Laboratory of Phylogenomics and Comparative Genomics, School of Life Sciences, Jiangsu Normal University, 221116 Xuzhou, Jiangsu China.</nlm:affiliation>
<wicri:noCountry code="subField">Jiangsu China</wicri:noCountry>
</affiliation>
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<author>
<name sortKey="Xuan, Ying" sort="Xuan, Ying" uniqKey="Xuan Y" first="Ying" last="Xuan">Ying Xuan</name>
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<nlm:affiliation>Jiangsu Key Laboratory of Phylogenomics and Comparative Genomics, School of Life Sciences, Jiangsu Normal University, 221116 Xuzhou, Jiangsu China.</nlm:affiliation>
<wicri:noCountry code="subField">Jiangsu China</wicri:noCountry>
</affiliation>
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<author>
<name sortKey="Bian, Xiaofeng" sort="Bian, Xiaofeng" uniqKey="Bian X" first="Xiaofeng" last="Bian">Xiaofeng Bian</name>
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<nlm:affiliation>Institute of Food Crops, Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, 210014 Nanjing, China.</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
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<wicri:noRegion>210014 Nanjing</wicri:noRegion>
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<name sortKey="Zhang, Lei" sort="Zhang, Lei" uniqKey="Zhang L" first="Lei" last="Zhang">Lei Zhang</name>
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<wicri:noCountry code="subField">Jiangsu China</wicri:noCountry>
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<name sortKey="Pan, Zhiyuan" sort="Pan, Zhiyuan" uniqKey="Pan Z" first="Zhiyuan" last="Pan">Zhiyuan Pan</name>
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<wicri:noCountry code="subField">Jiangsu China</wicri:noCountry>
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<name sortKey="Kou, Meng" sort="Kou, Meng" uniqKey="Kou M" first="Meng" last="Kou">Meng Kou</name>
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<div type="abstract" xml:lang="en">Phosphatidylserine synthase (PSS)-mediated phosphatidylserine (PS) synthesis is crucial for plant development. However, little is known about the contribution of PSS to Na
<sup>+</sup>
homeostasis regulation and salt tolerance in plants. Here, we cloned the
<i>IbPSS1</i>
gene, which encodes an ortholog of
<i>Arabidopsis AtPSS1</i>
, from sweet potato (
<i>Ipomoea batatas</i>
(L.) Lam.). The transient expression of
<i>IbPSS1</i>
in
<i>Nicotiana benthamiana</i>
leaves increased PS abundance. We then established an efficient
<i>Agrobacterium rhizogenes</i>
-mediated in vivo root transgenic system for sweet potato. Overexpression of
<i>IbPSS1</i>
through this system markedly decreased cellular Na
<sup>+</sup>
accumulation in salinized transgenic roots (TRs) compared with adventitious roots. The overexpression of
<i>IbPSS1</i>
enhanced salt-induced Na
<sup>+</sup>
/H
<sup>+</sup>
antiport activity and increased plasma membrane (PM) Ca
<sup>2+</sup>
-permeable channel sensitivity to NaCl and H
<sub>2</sub>
O
<sub>2</sub>
in the TRs. We confirmed the important role of
<i>IbPSS1</i>
in improving salt tolerance in transgenic sweet potato lines obtained from an
<i>Agrobacterium tumefaciens</i>
-mediated transformation system. Similarly, compared with the wild-type (WT) plants, the transgenic lines presented decreased Na
<sup>+</sup>
accumulation, enhanced Na
<sup>+</sup>
exclusion, and increased PM Ca
<sup>2+</sup>
-permeable channel sensitivity to NaCl and H
<sub>2</sub>
O
<sub>2</sub>
in the roots. Exogenous application of lysophosphatidylserine triggered similar shifts in Na
<sup>+</sup>
accumulation and Na
<sup>+</sup>
and Ca
<sup>2+</sup>
fluxes in the salinized roots of WT. Overall, this study provides an efficient and reliable transgenic method for functional genomic studies of sweet potato. Our results revealed that
<i>IbPSS1</i>
contributes to the salt tolerance of sweet potato by enabling Na
<sup>+</sup>
homeostasis and Na
<sup>+</sup>
exclusion in the roots, and the latter process is possibly controlled by PS reinforcing Ca
<sup>2+</sup>
signaling in the roots.</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM">
<PMID Version="1">32821414</PMID>
<DateRevised>
<Year>2020</Year>
<Month>09</Month>
<Day>28</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">2052-7276</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>7</Volume>
<PubDate>
<Year>2020</Year>
</PubDate>
</JournalIssue>
<Title>Horticulture research</Title>
<ISOAbbreviation>Hortic Res</ISOAbbreviation>
</Journal>
<ArticleTitle>Overexpression of phosphatidylserine synthase
<i>IbPSS1</i>
affords cellular Na
<sup>+</sup>
homeostasis and salt tolerance by activating plasma membrane Na
<sup>+</sup>
/H
<sup>+</sup>
antiport activity in sweet potato roots.</ArticleTitle>
<Pagination>
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</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1038/s41438-020-00358-1</ELocationID>
<Abstract>
<AbstractText>Phosphatidylserine synthase (PSS)-mediated phosphatidylserine (PS) synthesis is crucial for plant development. However, little is known about the contribution of PSS to Na
<sup>+</sup>
homeostasis regulation and salt tolerance in plants. Here, we cloned the
<i>IbPSS1</i>
gene, which encodes an ortholog of
<i>Arabidopsis AtPSS1</i>
, from sweet potato (
<i>Ipomoea batatas</i>
(L.) Lam.). The transient expression of
<i>IbPSS1</i>
in
<i>Nicotiana benthamiana</i>
leaves increased PS abundance. We then established an efficient
<i>Agrobacterium rhizogenes</i>
-mediated in vivo root transgenic system for sweet potato. Overexpression of
<i>IbPSS1</i>
through this system markedly decreased cellular Na
<sup>+</sup>
accumulation in salinized transgenic roots (TRs) compared with adventitious roots. The overexpression of
<i>IbPSS1</i>
enhanced salt-induced Na
<sup>+</sup>
/H
<sup>+</sup>
antiport activity and increased plasma membrane (PM) Ca
<sup>2+</sup>
-permeable channel sensitivity to NaCl and H
<sub>2</sub>
O
<sub>2</sub>
in the TRs. We confirmed the important role of
<i>IbPSS1</i>
in improving salt tolerance in transgenic sweet potato lines obtained from an
<i>Agrobacterium tumefaciens</i>
-mediated transformation system. Similarly, compared with the wild-type (WT) plants, the transgenic lines presented decreased Na
<sup>+</sup>
accumulation, enhanced Na
<sup>+</sup>
exclusion, and increased PM Ca
<sup>2+</sup>
-permeable channel sensitivity to NaCl and H
<sub>2</sub>
O
<sub>2</sub>
in the roots. Exogenous application of lysophosphatidylserine triggered similar shifts in Na
<sup>+</sup>
accumulation and Na
<sup>+</sup>
and Ca
<sup>2+</sup>
fluxes in the salinized roots of WT. Overall, this study provides an efficient and reliable transgenic method for functional genomic studies of sweet potato. Our results revealed that
<i>IbPSS1</i>
contributes to the salt tolerance of sweet potato by enabling Na
<sup>+</sup>
homeostasis and Na
<sup>+</sup>
exclusion in the roots, and the latter process is possibly controlled by PS reinforcing Ca
<sup>2+</sup>
signaling in the roots.</AbstractText>
<CopyrightInformation>© The Author(s) 2020.</CopyrightInformation>
</Abstract>
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<LastName>Zhang</LastName>
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<LastName>Kou</LastName>
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<Identifier Source="ISNI">0000 0000 9698 6425</Identifier>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District, 221131 Xuzhou, Jiangsu Province China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Cao</LastName>
<ForeName>Qinghe</ForeName>
<Initials>Q</Initials>
<AffiliationInfo>
<Affiliation>Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District, 221131 Xuzhou, Jiangsu Province China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Tang</LastName>
<ForeName>Zhonghou</ForeName>
<Initials>Z</Initials>
<AffiliationInfo>
<Affiliation>Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District, 221131 Xuzhou, Jiangsu Province China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Li</LastName>
<ForeName>Qiang</ForeName>
<Initials>Q</Initials>
<AffiliationInfo>
<Affiliation>Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District, 221131 Xuzhou, Jiangsu Province China.</Affiliation>
</AffiliationInfo>
</Author>
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<ForeName>Daifu</ForeName>
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<Affiliation>Xuzhou Institute of Agricultural Sciences in Jiangsu Xuhuai District, 221131 Xuzhou, Jiangsu Province China.</Affiliation>
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