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A transient transformation system for gene characterization in upland cotton (Gossypium hirsutum).

Identifieur interne : 000165 ( Main/Corpus ); précédent : 000164; suivant : 000166

A transient transformation system for gene characterization in upland cotton (Gossypium hirsutum).

Auteurs : Haipeng Li ; Kun Li ; Yutao Guo ; Jinggong Guo ; Kaiting Miao ; Jose R. Botella ; Chun-Peng Song ; Yuchen Miao

Source :

RBID : pubmed:29977323

Abstract

Background

Genetically modified cotton accounts for 64% of the world's cotton growing area (22.3 million hectares). The genome sequencing of the diploid cotton progenitors

Results

We developed a transient transformation system for gene characterization in upland cotton. Using β-glucuronidase as a reporter for

Conclusions

The 


DOI: 10.1186/s13007-018-0319-2
PubMed: 29977323
PubMed Central: PMC6013946

Links to Exploration step

pubmed:29977323

Le document en format XML

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<affiliation>
<nlm:affiliation>2School of Life Science, Southwest University, No. 1, Tiansheng Road, Beibei, Chongqing, 400715 China.</nlm:affiliation>
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<name sortKey="Botella, Jose R" sort="Botella, Jose R" uniqKey="Botella J" first="Jose R" last="Botella">Jose R. Botella</name>
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<nlm:affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</nlm:affiliation>
</affiliation>
<affiliation>
<nlm:affiliation>3School of Agriculture and Food Sciences, University of Queensland, Brisbane, QLD Australia.</nlm:affiliation>
</affiliation>
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<author>
<name sortKey="Song, Chun Peng" sort="Song, Chun Peng" uniqKey="Song C" first="Chun-Peng" last="Song">Chun-Peng Song</name>
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<nlm:affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</nlm:affiliation>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>Background</b>
</p>
<p>Genetically modified cotton accounts for 64% of the world's cotton growing area (22.3 million hectares). The genome sequencing of the diploid cotton progenitors </p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Results</b>
</p>
<p>We developed a transient transformation system for gene characterization in upland cotton. Using β-glucuronidase as a reporter for </p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>Conclusions</b>
</p>
<p>The </p>
</div>
</front>
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<PMID Version="1">29977323</PMID>
<DateRevised>
<Year>2020</Year>
<Month>10</Month>
<Day>01</Day>
</DateRevised>
<Article PubModel="Electronic-eCollection">
<Journal>
<ISSN IssnType="Print">1746-4811</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>14</Volume>
<PubDate>
<Year>2018</Year>
</PubDate>
</JournalIssue>
<Title>Plant methods</Title>
<ISOAbbreviation>Plant Methods</ISOAbbreviation>
</Journal>
<ArticleTitle>A transient transformation system for gene characterization in upland cotton (
<i>Gossypium hirsutum</i>
).</ArticleTitle>
<Pagination>
<MedlinePgn>50</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1186/s13007-018-0319-2</ELocationID>
<Abstract>
<AbstractText Label="Background" NlmCategory="UNASSIGNED">Genetically modified cotton accounts for 64% of the world's cotton growing area (22.3 million hectares). The genome sequencing of the diploid cotton progenitors
<i>Gossypium raimondii</i>
and
<i>Gossypium arboreum</i>
as well as the cultivated
<i>Gossypium hirsutum</i>
has provided a wealth of genetic information that could be exploited for crop improvement. Unfortunately, gene functional characterization in cotton is lagging behind other economically important crops due to the low efficiency, lengthiness and technical complexity of the available stable transformation methods. We present here a simple, fast and efficient method for the transient transformation of
<i>G</i>
.
<i>hirsutum</i>
that can be used for gene characterization studies.</AbstractText>
<AbstractText Label="Results" NlmCategory="UNASSIGNED">We developed a transient transformation system for gene characterization in upland cotton. Using β-glucuronidase as a reporter for
<i>Agrobacterium</i>
-mediated transformation assays, we evaluated multiple transformation parameters such as
<i>Agrobacterium</i>
strain, bacterial density, length of co-cultivation, chemicals and surfactants, which can affect transformation efficiency. After the initial characterization, the
<i>Agrobacterium</i>
EHA105 strain was selected and a number of binary constructs used to perform gene characterization studies. 7-days-old cotton seedlings were co-cultivated with
<i>Agrobacterium</i>
and transient gene expression was observed 5 days after infection of the plants. Transcript levels of two different transgenes under the control of the cauliflower mosaic virus (CaMV) 35S promoter were quantified by real-time reverse transcription PCR (qRT-PCR) showing a 3-10 times increase over the levels observed in non-infected controls. The expression patterns driven by the promoters of two
<i>G</i>
.
<i>hirsutum</i>
genes as well as the subcellular localization of their corresponding proteins were studied using the new transient expression system and our observations were consistent with previously published results using
<i>Arabidopsis</i>
as a heterologous system.</AbstractText>
<AbstractText Label="Conclusions" NlmCategory="UNASSIGNED">The 
<i>Agrobacterium</i>
-mediated transient transformation method is a fast and easy transient expression system enabling high transient expression and transformation efficiency in upland cotton seedlings. Our method can be used for gene functional studies such as promoter characterization and protein subcellular localization in cotton, obviating the need to perform such studies in a heterologous system such as
<i>Arabidopsis</i>
.</AbstractText>
</Abstract>
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<LastName>Li</LastName>
<ForeName>Haipeng</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
<Identifier Source="ISNI">0000 0000 9139 560X</Identifier>
<Identifier Source="GRID">grid.256922.8</Identifier>
</AffiliationInfo>
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<LastName>Li</LastName>
<ForeName>Kun</ForeName>
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<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
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<Identifier Source="GRID">grid.256922.8</Identifier>
</AffiliationInfo>
</Author>
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<LastName>Guo</LastName>
<ForeName>Yutao</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
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<Identifier Source="GRID">grid.256922.8</Identifier>
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<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
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<Initials>K</Initials>
<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
<Identifier Source="ISNI">0000 0000 9139 560X</Identifier>
<Identifier Source="GRID">grid.256922.8</Identifier>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>2School of Life Science, Southwest University, No. 1, Tiansheng Road, Beibei, Chongqing, 400715 China.</Affiliation>
<Identifier Source="GRID">grid.263906.8</Identifier>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Botella</LastName>
<ForeName>Jose R</ForeName>
<Initials>JR</Initials>
<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
<Identifier Source="ISNI">0000 0000 9139 560X</Identifier>
<Identifier Source="GRID">grid.256922.8</Identifier>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>3School of Agriculture and Food Sciences, University of Queensland, Brisbane, QLD Australia.</Affiliation>
<Identifier Source="ISNI">0000 0000 9320 7537</Identifier>
<Identifier Source="GRID">grid.1003.2</Identifier>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Song</LastName>
<ForeName>Chun-Peng</ForeName>
<Initials>CP</Initials>
<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
<Identifier Source="ISNI">0000 0000 9139 560X</Identifier>
<Identifier Source="GRID">grid.256922.8</Identifier>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Miao</LastName>
<ForeName>Yuchen</ForeName>
<Initials>Y</Initials>
<AffiliationInfo>
<Affiliation>1Institute of Plant Stress Biology, State Key Laboratory of Cotton Biology, Department of Biology, Henan University, 85 Minglun Street, Kaifeng, 475001 China.</Affiliation>
<Identifier Source="ISNI">0000 0000 9139 560X</Identifier>
<Identifier Source="GRID">grid.256922.8</Identifier>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2018</Year>
<Month>06</Month>
<Day>22</Day>
</ArticleDate>
</Article>
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<Country>England</Country>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Agrobacterium</Keyword>
<Keyword MajorTopicYN="N">Cotton</Keyword>
<Keyword MajorTopicYN="N">Gene characterization</Keyword>
<Keyword MajorTopicYN="N">Gossypium hirsutum</Keyword>
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<Month>06</Month>
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   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:29977323
   |texte=   A transient transformation system for gene characterization in upland cotton (Gossypium hirsutum).
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Corpus/RBID.i   -Sk "pubmed:29977323" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a AgrobacTransV1 

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