Serveur d'exploration sur la glutarédoxine

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cDNA cloning and expression analysis of glutaredoxin (Grx) 2 in the Pacific white shrimp Litopenaeus vannamei.

Identifieur interne : 000098 ( Main/Exploration ); précédent : 000097; suivant : 000099

cDNA cloning and expression analysis of glutaredoxin (Grx) 2 in the Pacific white shrimp Litopenaeus vannamei.

Auteurs : Pei-Hua Zheng [République populaire de Chine] ; Lei Wang [République populaire de Chine] ; An-Li Wang [République populaire de Chine] ; Xiu-Xia Zhang [République populaire de Chine] ; Jian-Min Ye [République populaire de Chine] ; Dong-Mei Wang [République populaire de Chine] ; Jing-Feng Sun [République populaire de Chine] ; Jun-Tao Li [République populaire de Chine] ; Yao-Peng Lu [République populaire de Chine] ; Jian-An Xian [République populaire de Chine]

Source :

RBID : pubmed:30537530

Descripteurs français

English descriptors

Abstract

Glutaredoxin (Grx) is a class molecule oxidoreductase, which can regulate the redox state of proteins and plays a key role in antioxidant defense. However, the informations of Grx cDNA sequences and their functions are lack in decapod crustacea. In the present study, the cDNA of LvGrx 2 was cloned from the Pacific white shrimp, Litopenaeus vannamei. The open reading frame (ORF) of LvGrx 2 was 360 bp, which encoded a polypeptide of 119 amino acids. The molecular mass of the predicted protein is 12.87 kDa with an estimated pI of 8.22. Sequence alignment showed that the amino acid sequence of LvGrx 2 shares 59%, 59% and 58% identity with that of the coelacanth Latimeria chalumnae, the plateau frog Nanorana parkeri and the half-smooth tongue sole Cynoglossus semilaevis, respectively. Quantitative real-time PCR analysis revealed that LvGrx 2 were detected in a wide range of tissues, with highest expression in gill, hepatopancrea and intestine, and weakest expression in muscle. The expression responses of LvGrx 2 were analyzed in hepatopancrea and gill after ammonia-N stress or lipopolysaccharide (LPS) injection. During ammonia-N exposure, the LvGrx 2 transcriptions in hepatopancrea and gill significantly up-regulated, and the peak value appeared after 12 h and 24 h exposure respectively. After LPS injection, expression levels of LvGrx 2 in hepatopancrea obviously increased in the early and late stages, while LvGrx 2 transcription in gill sharply up-regulated in the middle period. These results suggest that LvGrx 2 may play a vital role in shrimp defense system against environmental stress and pathogen infection. RNA interference experiment was designed to further probe roles of LvGrx 2 during ammonia-N exposure. Ammonia-N induced obvious improvement in expression levels of LvGrx 2, LvGrx 3, GPx, GST and Trx, accompanied by increases of protein carbonyl and malondialdehyde (MDA) contents. However, transcription of GPx and GST were much weaker in LvGrx 2 interfered-shrimp, and oxidative damage in both lipid and protein were more serious. These results further suggest that LvGrx 2 in shrimp participates in oxidative defence and regulation of antioxidant system.

DOI: 10.1016/j.fsi.2018.12.011
PubMed: 30537530


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<term>Ammonia (administration & dosage)</term>
<term>Animals (MeSH)</term>
<term>Cloning, Molecular (MeSH)</term>
<term>DNA, Complementary (genetics)</term>
<term>Gene Expression Profiling (MeSH)</term>
<term>Glutaredoxins (genetics)</term>
<term>Intestines (MeSH)</term>
<term>Lipopolysaccharides (administration & dosage)</term>
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<term>Sequence Alignment (MeSH)</term>
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<term>ADN complémentaire (génétique)</term>
<term>ARN messager (MeSH)</term>
<term>Alignement de séquences (MeSH)</term>
<term>Ammoniac (administration et posologie)</term>
<term>Analyse de profil d'expression de gènes (MeSH)</term>
<term>Animaux (MeSH)</term>
<term>Cadres ouverts de lecture (MeSH)</term>
<term>Clonage moléculaire (MeSH)</term>
<term>Glutarédoxines (génétique)</term>
<term>Intestins (MeSH)</term>
<term>Lipopolysaccharides (administration et posologie)</term>
<term>Muscles (MeSH)</term>
<term>Penaeidae (génétique)</term>
<term>Phylogenèse (MeSH)</term>
<term>Réaction de polymérisation en chaine en temps réel (MeSH)</term>
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<term>Ammonia</term>
<term>Lipopolysaccharides</term>
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<term>DNA, Complementary</term>
<term>Glutaredoxins</term>
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<term>Ammoniac</term>
<term>Lipopolysaccharides</term>
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<term>Penaeidae</term>
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<term>Animals</term>
<term>Cloning, Molecular</term>
<term>Gene Expression Profiling</term>
<term>Intestines</term>
<term>Muscles</term>
<term>Open Reading Frames</term>
<term>Phylogeny</term>
<term>RNA, Messenger</term>
<term>Real-Time Polymerase Chain Reaction</term>
<term>Sequence Alignment</term>
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<term>Analyse de profil d'expression de gènes</term>
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<term>Cadres ouverts de lecture</term>
<term>Clonage moléculaire</term>
<term>Intestins</term>
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<div type="abstract" xml:lang="en">Glutaredoxin (Grx) is a class molecule oxidoreductase, which can regulate the redox state of proteins and plays a key role in antioxidant defense. However, the informations of Grx cDNA sequences and their functions are lack in decapod crustacea. In the present study, the cDNA of LvGrx 2 was cloned from the Pacific white shrimp, Litopenaeus vannamei. The open reading frame (ORF) of LvGrx 2 was 360 bp, which encoded a polypeptide of 119 amino acids. The molecular mass of the predicted protein is 12.87 kDa with an estimated pI of 8.22. Sequence alignment showed that the amino acid sequence of LvGrx 2 shares 59%, 59% and 58% identity with that of the coelacanth Latimeria chalumnae, the plateau frog Nanorana parkeri and the half-smooth tongue sole Cynoglossus semilaevis, respectively. Quantitative real-time PCR analysis revealed that LvGrx 2 were detected in a wide range of tissues, with highest expression in gill, hepatopancrea and intestine, and weakest expression in muscle. The expression responses of LvGrx 2 were analyzed in hepatopancrea and gill after ammonia-N stress or lipopolysaccharide (LPS) injection. During ammonia-N exposure, the LvGrx 2 transcriptions in hepatopancrea and gill significantly up-regulated, and the peak value appeared after 12 h and 24 h exposure respectively. After LPS injection, expression levels of LvGrx 2 in hepatopancrea obviously increased in the early and late stages, while LvGrx 2 transcription in gill sharply up-regulated in the middle period. These results suggest that LvGrx 2 may play a vital role in shrimp defense system against environmental stress and pathogen infection. RNA interference experiment was designed to further probe roles of LvGrx 2 during ammonia-N exposure. Ammonia-N induced obvious improvement in expression levels of LvGrx 2, LvGrx 3, GPx, GST and Trx, accompanied by increases of protein carbonyl and malondialdehyde (MDA) contents. However, transcription of GPx and GST were much weaker in LvGrx 2 interfered-shrimp, and oxidative damage in both lipid and protein were more serious. These results further suggest that LvGrx 2 in shrimp participates in oxidative defence and regulation of antioxidant system.</div>
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<Year>2019</Year>
<Month>Mar</Month>
</PubDate>
</JournalIssue>
<Title>Fish & shellfish immunology</Title>
<ISOAbbreviation>Fish Shellfish Immunol</ISOAbbreviation>
</Journal>
<ArticleTitle>cDNA cloning and expression analysis of glutaredoxin (Grx) 2 in the Pacific white shrimp Litopenaeus vannamei.</ArticleTitle>
<Pagination>
<MedlinePgn>662-671</MedlinePgn>
</Pagination>
<ELocationID EIdType="pii" ValidYN="Y">S1050-4648(18)30810-6</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.fsi.2018.12.011</ELocationID>
<Abstract>
<AbstractText>Glutaredoxin (Grx) is a class molecule oxidoreductase, which can regulate the redox state of proteins and plays a key role in antioxidant defense. However, the informations of Grx cDNA sequences and their functions are lack in decapod crustacea. In the present study, the cDNA of LvGrx 2 was cloned from the Pacific white shrimp, Litopenaeus vannamei. The open reading frame (ORF) of LvGrx 2 was 360 bp, which encoded a polypeptide of 119 amino acids. The molecular mass of the predicted protein is 12.87 kDa with an estimated pI of 8.22. Sequence alignment showed that the amino acid sequence of LvGrx 2 shares 59%, 59% and 58% identity with that of the coelacanth Latimeria chalumnae, the plateau frog Nanorana parkeri and the half-smooth tongue sole Cynoglossus semilaevis, respectively. Quantitative real-time PCR analysis revealed that LvGrx 2 were detected in a wide range of tissues, with highest expression in gill, hepatopancrea and intestine, and weakest expression in muscle. The expression responses of LvGrx 2 were analyzed in hepatopancrea and gill after ammonia-N stress or lipopolysaccharide (LPS) injection. During ammonia-N exposure, the LvGrx 2 transcriptions in hepatopancrea and gill significantly up-regulated, and the peak value appeared after 12 h and 24 h exposure respectively. After LPS injection, expression levels of LvGrx 2 in hepatopancrea obviously increased in the early and late stages, while LvGrx 2 transcription in gill sharply up-regulated in the middle period. These results suggest that LvGrx 2 may play a vital role in shrimp defense system against environmental stress and pathogen infection. RNA interference experiment was designed to further probe roles of LvGrx 2 during ammonia-N exposure. Ammonia-N induced obvious improvement in expression levels of LvGrx 2, LvGrx 3, GPx, GST and Trx, accompanied by increases of protein carbonyl and malondialdehyde (MDA) contents. However, transcription of GPx and GST were much weaker in LvGrx 2 interfered-shrimp, and oxidative damage in both lipid and protein were more serious. These results further suggest that LvGrx 2 in shrimp participates in oxidative defence and regulation of antioxidant system.</AbstractText>
<CopyrightInformation>Copyright © 2018 Elsevier Ltd. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Zheng</LastName>
<ForeName>Pei-Hua</ForeName>
<Initials>PH</Initials>
<AffiliationInfo>
<Affiliation>Hainan Provincial Key Laboratory for Functional Components Research and Utilization of Marine Bio-resources, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, People's Republic of China; Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, School of Life Sciences, South China Normal University, Guangzhou, 510631, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>Lei</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Institute for Brain Research and Rehabilitation, South China Normal University, Guangzhou, 510631, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>An-Li</ForeName>
<Initials>AL</Initials>
<AffiliationInfo>
<Affiliation>Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, School of Life Sciences, South China Normal University, Guangzhou, 510631, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zhang</LastName>
<ForeName>Xiu-Xia</ForeName>
<Initials>XX</Initials>
<AffiliationInfo>
<Affiliation>Hainan Provincial Key Laboratory for Functional Components Research and Utilization of Marine Bio-resources, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Ye</LastName>
<ForeName>Jian-Min</ForeName>
<Initials>JM</Initials>
<AffiliationInfo>
<Affiliation>Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, School of Life Sciences, South China Normal University, Guangzhou, 510631, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wang</LastName>
<ForeName>Dong-Mei</ForeName>
<Initials>DM</Initials>
<AffiliationInfo>
<Affiliation>Hainan Provincial Key Laboratory for Functional Components Research and Utilization of Marine Bio-resources, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sun</LastName>
<ForeName>Jing-Feng</ForeName>
<Initials>JF</Initials>
<AffiliationInfo>
<Affiliation>Tianjin Key Laboratory of Aqua-ecology and Aquaculture, College of Fisheries, Tianjin Agricultural University, Tianjin, 300384, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Li</LastName>
<ForeName>Jun-Tao</ForeName>
<Initials>JT</Initials>
<AffiliationInfo>
<Affiliation>Hainan Provincial Key Laboratory for Functional Components Research and Utilization of Marine Bio-resources, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Lu</LastName>
<ForeName>Yao-Peng</ForeName>
<Initials>YP</Initials>
<AffiliationInfo>
<Affiliation>Hainan Provincial Key Laboratory for Functional Components Research and Utilization of Marine Bio-resources, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, People's Republic of China; Guangdong Provincial Key Laboratory for Healthy and Safe Aquaculture, School of Life Sciences, South China Normal University, Guangzhou, 510631, People's Republic of China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Xian</LastName>
<ForeName>Jian-An</ForeName>
<Initials>JA</Initials>
<AffiliationInfo>
<Affiliation>Hainan Provincial Key Laboratory for Functional Components Research and Utilization of Marine Bio-resources, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, People's Republic of China. Electronic address: xian-ja@163.com.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2018</Year>
<Month>12</Month>
<Day>08</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>England</Country>
<MedlineTA>Fish Shellfish Immunol</MedlineTA>
<NlmUniqueID>9505220</NlmUniqueID>
<ISSNLinking>1050-4648</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D018076">DNA, Complementary</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D054477">Glutaredoxins</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008070">Lipopolysaccharides</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>7664-41-7</RegistryNumber>
<NameOfSubstance UI="D000641">Ammonia</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000641" MajorTopicYN="N">Ammonia</DescriptorName>
<QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018076" MajorTopicYN="N">DNA, Complementary</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D054477" MajorTopicYN="N">Glutaredoxins</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D007422" MajorTopicYN="N">Intestines</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D008070" MajorTopicYN="N">Lipopolysaccharides</DescriptorName>
<QualifierName UI="Q000008" MajorTopicYN="N">administration & dosage</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D009132" MajorTopicYN="N">Muscles</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016366" MajorTopicYN="N">Open Reading Frames</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D033561" MajorTopicYN="N">Penaeidae</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D060888" MajorTopicYN="N">Real-Time Polymerase Chain Reaction</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D016415" MajorTopicYN="N">Sequence Alignment</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Ammonia</Keyword>
<Keyword MajorTopicYN="N">Expression</Keyword>
<Keyword MajorTopicYN="N">Glutaredoxin</Keyword>
<Keyword MajorTopicYN="N">Immunity</Keyword>
<Keyword MajorTopicYN="N">Lipopolysaccharide</Keyword>
<Keyword MajorTopicYN="N">Litopenaeus vannamei</Keyword>
</KeywordList>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="received">
<Year>2018</Year>
<Month>01</Month>
<Day>03</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2018</Year>
<Month>11</Month>
<Day>29</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2018</Year>
<Month>12</Month>
<Day>07</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2018</Year>
<Month>12</Month>
<Day>12</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2019</Year>
<Month>5</Month>
<Day>24</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez">
<Year>2018</Year>
<Month>12</Month>
<Day>12</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">30537530</ArticleId>
<ArticleId IdType="pii">S1050-4648(18)30810-6</ArticleId>
<ArticleId IdType="doi">10.1016/j.fsi.2018.12.011</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations>
<list>
<country>
<li>République populaire de Chine</li>
</country>
</list>
<tree>
<country name="République populaire de Chine">
<noRegion>
<name sortKey="Zheng, Pei Hua" sort="Zheng, Pei Hua" uniqKey="Zheng P" first="Pei-Hua" last="Zheng">Pei-Hua Zheng</name>
</noRegion>
<name sortKey="Li, Jun Tao" sort="Li, Jun Tao" uniqKey="Li J" first="Jun-Tao" last="Li">Jun-Tao Li</name>
<name sortKey="Lu, Yao Peng" sort="Lu, Yao Peng" uniqKey="Lu Y" first="Yao-Peng" last="Lu">Yao-Peng Lu</name>
<name sortKey="Sun, Jing Feng" sort="Sun, Jing Feng" uniqKey="Sun J" first="Jing-Feng" last="Sun">Jing-Feng Sun</name>
<name sortKey="Wang, An Li" sort="Wang, An Li" uniqKey="Wang A" first="An-Li" last="Wang">An-Li Wang</name>
<name sortKey="Wang, Dong Mei" sort="Wang, Dong Mei" uniqKey="Wang D" first="Dong-Mei" last="Wang">Dong-Mei Wang</name>
<name sortKey="Wang, Lei" sort="Wang, Lei" uniqKey="Wang L" first="Lei" last="Wang">Lei Wang</name>
<name sortKey="Xian, Jian An" sort="Xian, Jian An" uniqKey="Xian J" first="Jian-An" last="Xian">Jian-An Xian</name>
<name sortKey="Ye, Jian Min" sort="Ye, Jian Min" uniqKey="Ye J" first="Jian-Min" last="Ye">Jian-Min Ye</name>
<name sortKey="Zhang, Xiu Xia" sort="Zhang, Xiu Xia" uniqKey="Zhang X" first="Xiu-Xia" last="Zhang">Xiu-Xia Zhang</name>
</country>
</tree>
</affiliations>
</record>

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