Identification of glutaredoxin 1 and glutaredoxin 2 genes from Venerupis philippinarum and their responses to benzo[a]pyrene and bacterial challenge.
Identifieur interne : 000852 ( Main/Exploration ); précédent : 000851; suivant : 000853Identification of glutaredoxin 1 and glutaredoxin 2 genes from Venerupis philippinarum and their responses to benzo[a]pyrene and bacterial challenge.
Auteurs : Changkao Mu [République populaire de Chine] ; Qing Wang ; Zeyi Yuan ; Zhendong Zhang ; Chunlin WangSource :
- Fish & shellfish immunology [ 1095-9947 ] ; 2012.
Descripteurs français
- KwdFr :
- Alignement de séquences (MeSH), Analyse de profil d'expression de gènes (MeSH), Animaux (MeSH), Benzo[a]pyrène (pharmacologie), Bivalvia (classification), Bivalvia (génétique), Bivalvia (immunologie), Bivalvia (microbiologie), Bivalvia (métabolisme), Clonage moléculaire (MeSH), Données de séquences moléculaires (MeSH), Glutarédoxines (MeSH), Hémocytes (immunologie), Hépatopancréas (immunologie), Phylogenèse (MeSH), Phénomènes physiologiques bactériens (MeSH), Polluants chimiques de l'eau (pharmacologie), Régulation de l'expression des gènes (effets des médicaments et des substances chimiques), Similitude de séquences d'acides nucléiques (MeSH), Séquence d'acides aminés (MeSH), Séquence nucléotidique (MeSH).
- MESH :
- effets des médicaments et des substances chimiques : Régulation de l'expression des gènes.
- génétique : Bivalvia.
- immunologie : Bivalvia, Hémocytes, Hépatopancréas.
- microbiologie : Bivalvia.
- métabolisme : Bivalvia.
- pharmacologie : Benzo[a]pyrène, Bivalvia, Polluants chimiques de l'eau.
- Alignement de séquences, Analyse de profil d'expression de gènes, Animaux, Clonage moléculaire, Données de séquences moléculaires, Glutarédoxines, Phylogenèse, Phénomènes physiologiques bactériens, Similitude de séquences d'acides nucléiques, Séquence d'acides aminés, Séquence nucléotidique.
English descriptors
- KwdEn :
- Amino Acid Sequence (MeSH), Animals (MeSH), Bacterial Physiological Phenomena (MeSH), Base Sequence (MeSH), Benzo(a)pyrene (pharmacology), Bivalvia (classification), Bivalvia (genetics), Bivalvia (immunology), Bivalvia (metabolism), Bivalvia (microbiology), Cloning, Molecular (MeSH), Gene Expression Profiling (MeSH), Gene Expression Regulation (drug effects), Glutaredoxins (MeSH), Hemocytes (immunology), Hepatopancreas (immunology), Molecular Sequence Data (MeSH), Phylogeny (MeSH), Sequence Alignment (MeSH), Sequence Homology, Nucleic Acid (MeSH), Water Pollutants, Chemical (pharmacology).
- MESH :
- chemical , pharmacology : Benzo(a)pyrene, Water Pollutants, Chemical.
- classification : Bivalvia.
- drug effects : Gene Expression Regulation.
- genetics : Bivalvia.
- immunology : Bivalvia, Hemocytes, Hepatopancreas.
- metabolism : Bivalvia.
- microbiology : Bivalvia.
- Amino Acid Sequence, Animals, Bacterial Physiological Phenomena, Base Sequence, Cloning, Molecular, Gene Expression Profiling, Glutaredoxins, Molecular Sequence Data, Phylogeny, Sequence Alignment, Sequence Homology, Nucleic Acid.
Abstract
Glutaredoxin (abbreviated as Grx) is an important ubiquitous disulfide reductase, which can protect organisms against oxidative stresses. In the present study, a monothiol glutaredoxin gene (named as VpGrx1) and a dithiol glutaredoxin gene (named as VpGrx2) were identified from Venerupis philippinarum. Similar to most Grx2s, VpGrx2 possessed the conserved catalytic residues (C-P-Y-C) and other conserved features critical for the fundamental structure and function of Grx2s, while the active motif (C-G-Y-S) of VpGrx1 was different from the counterpart in other Grx1s. Quantitative Real-time PCR assay showed that VpGrx1 and VpGrx2 transcripts were detected in a wide range of tissues and mainly distributed in gills and hepatopancreas. After Vibrio challenge, both the expression levels of VpGrx1 and VpGrx2 mRNA in hemocytes were significantly up-regulated at 24 h. As concerned to benzo[a]pyrene (BaP) exposure, the expression levels of VpGrx1 and VpGrx2 transcripts in hepatopancreas were also significantly induced at 24 h. These results suggested that ROS could be induced through the respiratory burst to clear the invading bacteria and pollutants. VpGrx1 and VpGrx2 perhaps involved in the regulation of redox homeostasis and innate immune responses of V. philippinarum.
DOI: 10.1016/j.fsi.2011.12.001
PubMed: 22197689
Affiliations:
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challenge.</title><author><name sortKey="Mu, Changkao" sort="Mu, Changkao" uniqKey="Mu C" first="Changkao" last="Mu">Changkao Mu</name><affiliation wicri:level="1"><nlm:affiliation>School of Marine Science of Ningbo University, Ningbo 315211, PR China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>School of Marine Science of Ningbo University, Ningbo 315211</wicri:regionArea><wicri:noRegion>Ningbo 315211</wicri:noRegion></affiliation></author><author><name sortKey="Wang, Qing" sort="Wang, Qing" uniqKey="Wang Q" first="Qing" last="Wang">Qing Wang</name></author><author><name sortKey="Yuan, Zeyi" sort="Yuan, Zeyi" uniqKey="Yuan Z" first="Zeyi" last="Yuan">Zeyi Yuan</name></author><author><name sortKey="Zhang, Zhendong" sort="Zhang, Zhendong" uniqKey="Zhang Z" first="Zhendong" last="Zhang">Zhendong Zhang</name></author><author><name sortKey="Wang, Chunlin" sort="Wang, Chunlin" uniqKey="Wang C" first="Chunlin" last="Wang">Chunlin 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séquences d'acides nucléiques (MeSH)</term><term>Séquence d'acides aminés (MeSH)</term><term>Séquence nucléotidique (MeSH)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Benzo(a)pyrene</term><term>Water Pollutants, Chemical</term></keywords><keywords scheme="MESH" qualifier="classification" xml:lang="en"><term>Bivalvia</term></keywords><keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Gene Expression Regulation</term></keywords><keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr"><term>Régulation de l'expression des gènes</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Bivalvia</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Bivalvia</term></keywords><keywords scheme="MESH" qualifier="immunologie" 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In the present study, a monothiol glutaredoxin gene (named as VpGrx1) and a dithiol glutaredoxin gene (named as VpGrx2) were identified from Venerupis philippinarum. Similar to most Grx2s, VpGrx2 possessed the conserved catalytic residues (C-P-Y-C) and other conserved features critical for the fundamental structure and function of Grx2s, while the active motif (C-G-Y-S) of VpGrx1 was different from the counterpart in other Grx1s. Quantitative Real-time PCR assay showed that VpGrx1 and VpGrx2 transcripts were detected in a wide range of tissues and mainly distributed in gills and hepatopancreas. After Vibrio challenge, both the expression levels of VpGrx1 and VpGrx2 mRNA in hemocytes were significantly up-regulated at 24 h. As concerned to benzo[a]pyrene (BaP) exposure, the expression levels of VpGrx1 and VpGrx2 transcripts in hepatopancreas were also significantly induced at 24 h. These results suggested that ROS could be induced through the respiratory burst to clear the invading bacteria and pollutants. VpGrx1 and VpGrx2 perhaps involved in the regulation of redox homeostasis and innate immune responses of V. philippinarum.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">22197689</PMID><DateCompleted><Year>2012</Year><Month>05</Month><Day>25</Day></DateCompleted><DateRevised><Year>2013</Year><Month>11</Month><Day>21</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1095-9947</ISSN><JournalIssue CitedMedium="Internet"><Volume>32</Volume><Issue>3</Issue><PubDate><Year>2012</Year><Month>Mar</Month></PubDate></JournalIssue><Title>Fish & shellfish immunology</Title><ISOAbbreviation>Fish Shellfish Immunol</ISOAbbreviation></Journal><ArticleTitle>Identification of glutaredoxin 1 and glutaredoxin 2 genes from Venerupis philippinarum and their responses to benzo[a]pyrene and bacterial challenge.</ArticleTitle><Pagination><MedlinePgn>482-8</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.fsi.2011.12.001</ELocationID><Abstract><AbstractText>Glutaredoxin (abbreviated as Grx) is an important ubiquitous disulfide reductase, which can protect organisms against oxidative stresses. In the present study, a monothiol glutaredoxin gene (named as VpGrx1) and a dithiol glutaredoxin gene (named as VpGrx2) were identified from Venerupis philippinarum. Similar to most Grx2s, VpGrx2 possessed the conserved catalytic residues (C-P-Y-C) and other conserved features critical for the fundamental structure and function of Grx2s, while the active motif (C-G-Y-S) of VpGrx1 was different from the counterpart in other Grx1s. Quantitative Real-time PCR assay showed that VpGrx1 and VpGrx2 transcripts were detected in a wide range of tissues and mainly distributed in gills and hepatopancreas. After Vibrio challenge, both the expression levels of VpGrx1 and VpGrx2 mRNA in hemocytes were significantly up-regulated at 24 h. As concerned to benzo[a]pyrene (BaP) exposure, the expression levels of VpGrx1 and VpGrx2 transcripts in hepatopancreas were also significantly induced at 24 h. These results suggested that ROS could be induced through the respiratory burst to clear the invading bacteria and pollutants. VpGrx1 and VpGrx2 perhaps involved in the regulation of redox homeostasis and innate immune responses of V. philippinarum.</AbstractText><CopyrightInformation>Copyright © 2011 Elsevier Ltd. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Mu</LastName><ForeName>Changkao</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>School of Marine Science of Ningbo University, Ningbo 315211, PR China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Qing</ForeName><Initials>Q</Initials></Author><Author ValidYN="Y"><LastName>Yuan</LastName><ForeName>Zeyi</ForeName><Initials>Z</Initials></Author><Author ValidYN="Y"><LastName>Zhang</LastName><ForeName>Zhendong</ForeName><Initials>Z</Initials></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Chunlin</ForeName><Initials>C</Initials></Author></AuthorList><Language>eng</Language><DataBankList 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MajorTopicYN="N">classification</QualifierName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D020869" MajorTopicYN="N">Gene Expression Profiling</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005786" MajorTopicYN="N">Gene Expression Regulation</DescriptorName><QualifierName UI="Q000187" MajorTopicYN="Y">drug effects</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D054477" MajorTopicYN="N">Glutaredoxins</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006434" MajorTopicYN="N">Hemocytes</DescriptorName><QualifierName UI="Q000276" 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Chine</li></country></list><tree><noCountry><name sortKey="Wang, Chunlin" sort="Wang, Chunlin" uniqKey="Wang C" first="Chunlin" last="Wang">Chunlin Wang</name><name sortKey="Wang, Qing" sort="Wang, Qing" uniqKey="Wang Q" first="Qing" last="Wang">Qing Wang</name><name sortKey="Yuan, Zeyi" sort="Yuan, Zeyi" uniqKey="Yuan Z" first="Zeyi" last="Yuan">Zeyi Yuan</name><name sortKey="Zhang, Zhendong" sort="Zhang, Zhendong" uniqKey="Zhang Z" first="Zhendong" last="Zhang">Zhendong Zhang</name></noCountry><country name="République populaire de Chine"><noRegion><name sortKey="Mu, Changkao" sort="Mu, Changkao" uniqKey="Mu C" first="Changkao" last="Mu">Changkao Mu</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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