Expression of feline angiotensin converting enzyme 2 and its interaction with SARS-CoV S1 protein.
Identifieur interne : 001A26 ( Ncbi/Merge ); précédent : 001A25; suivant : 001A27Expression of feline angiotensin converting enzyme 2 and its interaction with SARS-CoV S1 protein.
Auteurs : Hongyan Guo [République populaire de Chine] ; Aizhen Guo ; Chong Wang ; Bangfen Yan ; Haisong Lu ; Huanchun ChenSource :
- Research in veterinary science [ 0034-5288 ] ; 2008.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Peptidyl-Dipeptidase A.
- chemical , metabolism : Viral Matrix Proteins.
- chemical : DNA Primers.
- Amino Acid Sequence, Animals, Cats, Cloning, Molecular, Conserved Sequence, Dogs, Gene Amplification, Humans, Mice, Molecular Sequence Data, Rats, SARS Virus, Viverridae.
Abstract
Feline angiotensin converting enzyme 2 (fACE2) gene was amplified from domestic cat lung with RT-PCR, cloned and sequenced. The complete coding region is 2418bp in length and is the closest to human ACE2 among known ACE2 homologs of non-primate animals. The N terminal fragment 19- 367 aa was expressed in Escherishia coli. Both Western blotting and ELISA demonstrated that fACE2 could react with SARS-CoV S1 protein as efficiently as ACE2 of Vero E6 cells did.
DOI: 10.1016/j.rvsc.2007.05.011
PubMed: 17658563
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type="chemical" qualifier="genetics" xml:lang="en"><term>Peptidyl-Dipeptidase A</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Viral Matrix Proteins</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>DNA Primers</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Peptidyl-Dipeptidase A</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Protéines de la matrice virale</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term><term>Animals</term><term>Cats</term><term>Cloning, Molecular</term><term>Conserved Sequence</term><term>Dogs</term><term>Gene Amplification</term><term>Humans</term><term>Mice</term><term>Molecular Sequence Data</term><term>Rats</term><term>SARS Virus</term><term>Viverridae</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Amorces ADN</term><term>Amplification de gène</term><term>Animaux</term><term>Chats</term><term>Chiens</term><term>Clonage moléculaire</term><term>Données de séquences moléculaires</term><term>Humains</term><term>Rats</term><term>Souris</term><term>Séquence conservée</term><term>Séquence d'acides aminés</term><term>Virus du SRAS</term><term>Viverridae</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Feline angiotensin converting enzyme 2 (fACE2) gene was amplified from domestic cat lung with RT-PCR, cloned and sequenced. The complete coding region is 2418bp in length and is the closest to human ACE2 among known ACE2 homologs of non-primate animals. The N terminal fragment 19- 367 aa was expressed in Escherishia coli. Both Western blotting and ELISA demonstrated that fACE2 could react with SARS-CoV S1 protein as efficiently as ACE2 of Vero E6 cells did.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">17658563</PMID><DateCompleted><Year>2008</Year><Month>08</Month><Day>11</Day></DateCompleted><DateRevised><Year>2020</Year><Month>04</Month><Day>03</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0034-5288</ISSN><JournalIssue CitedMedium="Print"><Volume>84</Volume><Issue>3</Issue><PubDate><Year>2008</Year><Month>Jun</Month></PubDate></JournalIssue><Title>Research in veterinary science</Title><ISOAbbreviation>Res. Vet. Sci.</ISOAbbreviation></Journal><ArticleTitle>Expression of feline angiotensin converting enzyme 2 and its interaction with SARS-CoV S1 protein.</ArticleTitle><Pagination><MedlinePgn>494-6</MedlinePgn></Pagination><Abstract><AbstractText>Feline angiotensin converting enzyme 2 (fACE2) gene was amplified from domestic cat lung with RT-PCR, cloned and sequenced. The complete coding region is 2418bp in length and is the closest to human ACE2 among known ACE2 homologs of non-primate animals. The N terminal fragment 19- 367 aa was expressed in Escherishia coli. 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A</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.4.17.-</RegistryNumber><NameOfSubstance UI="C413524">angiotensin converting enzyme 2</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000595" MajorTopicYN="N">Amino Acid Sequence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002415" MajorTopicYN="N">Cats</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017124" MajorTopicYN="N">Conserved Sequence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D017931" MajorTopicYN="N">DNA Primers</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004285" MajorTopicYN="N">Dogs</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005784" 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Aizhen" uniqKey="Guo A" first="Aizhen" last="Guo">Aizhen Guo</name><name sortKey="Lu, Haisong" sort="Lu, Haisong" uniqKey="Lu H" first="Haisong" last="Lu">Haisong Lu</name><name sortKey="Wang, Chong" sort="Wang, Chong" uniqKey="Wang C" first="Chong" last="Wang">Chong Wang</name><name sortKey="Yan, Bangfen" sort="Yan, Bangfen" uniqKey="Yan B" first="Bangfen" last="Yan">Bangfen Yan</name></noCountry><country name="République populaire de Chine"><region name="Hubei"><name sortKey="Guo, Hongyan" sort="Guo, Hongyan" uniqKey="Guo H" first="Hongyan" last="Guo">Hongyan Guo</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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