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Overexpression of PsnSuSy1, 2 genes enhances secondary cell wall thickening, vegetative growth, and mechanical strength in transgenic tobacco.

Identifieur interne : 000804 ( Main/Exploration ); précédent : 000803; suivant : 000805

Overexpression of PsnSuSy1, 2 genes enhances secondary cell wall thickening, vegetative growth, and mechanical strength in transgenic tobacco.

Auteurs : Meilang Li [République populaire de Chine] ; Shuan Wang [République populaire de Chine] ; Yingying Liu [République populaire de Chine] ; Yang Zhang [République populaire de Chine] ; Menxuan Ren [République populaire de Chine] ; Lulu Liu [République populaire de Chine] ; Tingting Lu [République populaire de Chine] ; Hairong Wei [États-Unis] ; Zhigang Wei [République populaire de Chine]

Source :

RBID : pubmed:31053988

Descripteurs français

English descriptors

Abstract

KEY MESSAGE

Two homologs PsnSuSy1 and PsnSuSy2 from poplar played largely similar but little distinct roles in modulating sink strength, accelerating vegetative growth and modifying secondary growth of plant. Co-overexpression of them together resulted in small but perceptible additive effects. Sucrose synthase (SuSy) acts as a crucial determinant of sink strength by controlling the conversion of sucrose into UDP-glucose, which is not only the sole precursor for cellulose biosynthesis but also an extracellular signaling molecule for plants growth. Therefore, modification of SuSy activity in plants is of utmost importance. We have isolated two SuSy genes from poplar, PsnSuSy1 and PsnSuSy2, which were preferentially expressed in secondary xylem/phloem. To investigate their functions, T2 tobacco transgenic lines of PsnSuSy1 and PsnSuSy2 were generated and then crossed to generate PsnSuSy1/PsnSuSy2 dual overexpression transgenic lines. SuSy activities in all lines were significantly increased though PsnSuSy1/PsnSuSy2 lines only exhibited slightly higher SuSy activities than either PsnSuSy1 or PsnSuSy2 lines. The significantly increased fructose and glucose, engendered by augmented SuSy activities, caused the alternations of many physiological, biochemical measures and phenotypic traits that include accelerated vegetative growth, thickened secondary cell wall, and increased stem breaking force, accompanied with altered expression levels of related pathway genes. The correlation relationships between SuSy activities and many of these traits were statistically significant. However, differences of almost all traits among three types of transgenic lines were insignificant. These findings clearly demonstrated that PsnSuSy1 and PsnSuSy2 had similar but little distinct functions and insubstantial additive effects on modulating sink strength and affecting allocation of carbon elements among secondary cell wall components.


DOI: 10.1007/s11103-019-00850-w
PubMed: 31053988


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Cell Wall (metabolism)</term>
<term>Cell Wall (ultrastructure)</term>
<term>Cellulose (biosynthesis)</term>
<term>Chlorophyll (analysis)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Genes, Plant (genetics)</term>
<term>Glucosyltransferases (genetics)</term>
<term>Glucosyltransferases (metabolism)</term>
<term>Lignin (metabolism)</term>
<term>Phloem (metabolism)</term>
<term>Photosynthesis (MeSH)</term>
<term>Plant Proteins (genetics)</term>
<term>Plants, Genetically Modified (genetics)</term>
<term>Polysaccharides (metabolism)</term>
<term>Populus (genetics)</term>
<term>Sequence Analysis (MeSH)</term>
<term>Sucrose (metabolism)</term>
<term>Tobacco (cytology)</term>
<term>Tobacco (genetics)</term>
<term>Tobacco (growth & development)</term>
<term>Xylem (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Analyse de séquence (MeSH)</term>
<term>Cellulose (biosynthèse)</term>
<term>Chlorophylle (analyse)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Glucosyltransferases (génétique)</term>
<term>Glucosyltransferases (métabolisme)</term>
<term>Gènes de plante (génétique)</term>
<term>Lignine (métabolisme)</term>
<term>Paroi cellulaire (métabolisme)</term>
<term>Paroi cellulaire (ultrastructure)</term>
<term>Phloème (métabolisme)</term>
<term>Photosynthèse (MeSH)</term>
<term>Polyosides (métabolisme)</term>
<term>Populus (génétique)</term>
<term>Protéines végétales (génétique)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Saccharose (métabolisme)</term>
<term>Tabac (croissance et développement)</term>
<term>Tabac (cytologie)</term>
<term>Tabac (génétique)</term>
<term>Végétaux génétiquement modifiés (génétique)</term>
<term>Xylème (métabolisme)</term>
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<term>Chlorophyll</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Cellulose</term>
</keywords>
<keywords scheme="MESH" qualifier="analyse" xml:lang="fr">
<term>Chlorophylle</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>Cellulose</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Tabac</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr">
<term>Tabac</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en">
<term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Genes, Plant</term>
<term>Glucosyltransferases</term>
<term>Plant Proteins</term>
<term>Plants, Genetically Modified</term>
<term>Populus</term>
<term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="growth & development" xml:lang="en">
<term>Tobacco</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Glucosyltransferases</term>
<term>Gènes de plante</term>
<term>Populus</term>
<term>Protéines végétales</term>
<term>Tabac</term>
<term>Végétaux génétiquement modifiés</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Cell Wall</term>
<term>Glucosyltransferases</term>
<term>Lignin</term>
<term>Phloem</term>
<term>Polysaccharides</term>
<term>Sucrose</term>
<term>Xylem</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Glucosyltransferases</term>
<term>Lignine</term>
<term>Paroi cellulaire</term>
<term>Phloème</term>
<term>Polyosides</term>
<term>Saccharose</term>
<term>Xylème</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="en">
<term>Cell Wall</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Cloning, Molecular</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation, Plant</term>
<term>Photosynthesis</term>
<term>Sequence Analysis</term>
</keywords>
<keywords scheme="MESH" qualifier="ultrastructure" xml:lang="fr">
<term>Analyse de profil d'expression de gènes</term>
<term>Analyse de séquence</term>
<term>Clonage moléculaire</term>
<term>Paroi cellulaire</term>
<term>Photosynthèse</term>
<term>Régulation de l'expression des gènes végétaux</term>
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<p>
<b>KEY MESSAGE</b>
</p>
<p>Two homologs PsnSuSy1 and PsnSuSy2 from poplar played largely similar but little distinct roles in modulating sink strength, accelerating vegetative growth and modifying secondary growth of plant. Co-overexpression of them together resulted in small but perceptible additive effects. Sucrose synthase (SuSy) acts as a crucial determinant of sink strength by controlling the conversion of sucrose into UDP-glucose, which is not only the sole precursor for cellulose biosynthesis but also an extracellular signaling molecule for plants growth. Therefore, modification of SuSy activity in plants is of utmost importance. We have isolated two SuSy genes from poplar, PsnSuSy1 and PsnSuSy2, which were preferentially expressed in secondary xylem/phloem. To investigate their functions, T2 tobacco transgenic lines of PsnSuSy1 and PsnSuSy2 were generated and then crossed to generate PsnSuSy1/PsnSuSy2 dual overexpression transgenic lines. SuSy activities in all lines were significantly increased though PsnSuSy1/PsnSuSy2 lines only exhibited slightly higher SuSy activities than either PsnSuSy1 or PsnSuSy2 lines. The significantly increased fructose and glucose, engendered by augmented SuSy activities, caused the alternations of many physiological, biochemical measures and phenotypic traits that include accelerated vegetative growth, thickened secondary cell wall, and increased stem breaking force, accompanied with altered expression levels of related pathway genes. The correlation relationships between SuSy activities and many of these traits were statistically significant. However, differences of almost all traits among three types of transgenic lines were insignificant. These findings clearly demonstrated that PsnSuSy1 and PsnSuSy2 had similar but little distinct functions and insubstantial additive effects on modulating sink strength and affecting allocation of carbon elements among secondary cell wall components.</p>
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<DateCompleted>
<Year>2019</Year>
<Month>06</Month>
<Day>07</Day>
</DateCompleted>
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<Year>2020</Year>
<Month>02</Month>
<Day>25</Day>
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<ISSN IssnType="Electronic">1573-5028</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>100</Volume>
<Issue>3</Issue>
<PubDate>
<Year>2019</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Plant molecular biology</Title>
<ISOAbbreviation>Plant Mol Biol</ISOAbbreviation>
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<ArticleTitle>Overexpression of PsnSuSy1, 2 genes enhances secondary cell wall thickening, vegetative growth, and mechanical strength in transgenic tobacco.</ArticleTitle>
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<Abstract>
<AbstractText Label="KEY MESSAGE" NlmCategory="UNASSIGNED">Two homologs PsnSuSy1 and PsnSuSy2 from poplar played largely similar but little distinct roles in modulating sink strength, accelerating vegetative growth and modifying secondary growth of plant. Co-overexpression of them together resulted in small but perceptible additive effects. Sucrose synthase (SuSy) acts as a crucial determinant of sink strength by controlling the conversion of sucrose into UDP-glucose, which is not only the sole precursor for cellulose biosynthesis but also an extracellular signaling molecule for plants growth. Therefore, modification of SuSy activity in plants is of utmost importance. We have isolated two SuSy genes from poplar, PsnSuSy1 and PsnSuSy2, which were preferentially expressed in secondary xylem/phloem. To investigate their functions, T2 tobacco transgenic lines of PsnSuSy1 and PsnSuSy2 were generated and then crossed to generate PsnSuSy1/PsnSuSy2 dual overexpression transgenic lines. SuSy activities in all lines were significantly increased though PsnSuSy1/PsnSuSy2 lines only exhibited slightly higher SuSy activities than either PsnSuSy1 or PsnSuSy2 lines. The significantly increased fructose and glucose, engendered by augmented SuSy activities, caused the alternations of many physiological, biochemical measures and phenotypic traits that include accelerated vegetative growth, thickened secondary cell wall, and increased stem breaking force, accompanied with altered expression levels of related pathway genes. The correlation relationships between SuSy activities and many of these traits were statistically significant. However, differences of almost all traits among three types of transgenic lines were insignificant. These findings clearly demonstrated that PsnSuSy1 and PsnSuSy2 had similar but little distinct functions and insubstantial additive effects on modulating sink strength and affecting allocation of carbon elements among secondary cell wall components.</AbstractText>
</Abstract>
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<LastName>Li</LastName>
<ForeName>Meilang</ForeName>
<Initials>M</Initials>
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<Affiliation>State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 150040, Heilongjiang, People's Republic of China.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>Shuan</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin, 150040, Heilongjiang, People's Republic of China.</Affiliation>
</AffiliationInfo>
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</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Bois/explor/PoplarV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000804 | SxmlIndent | more

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Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
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   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     pubmed:31053988
   |texte=   Overexpression of PsnSuSy1, 2 genes enhances secondary cell wall thickening, vegetative growth, and mechanical strength in transgenic tobacco.
}}

Pour générer des pages wiki

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