Widespread expression of PICOT in mouse and human tissues with predominant localization to epithelium.
Identifieur interne : 000973 ( Main/Exploration ); précédent : 000972; suivant : 000974Widespread expression of PICOT in mouse and human tissues with predominant localization to epithelium.
Auteurs : Ariel Ohayon [Israël] ; Yael Babichev ; Moran Galperin ; Amnon Altman ; Noah IsakovSource :
- The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society [ 1551-5044 ] ; 2010.
Descripteurs français
- KwdFr :
- ARN messager (biosynthèse), Animaux (MeSH), Cellules COS (MeSH), Humains (MeSH), Lignée cellulaire tumorale (MeSH), Protein-disulfide reductase (glutathione) (MeSH), Protéines de transport (biosynthèse), Protéines de transport (génétique), Souris (MeSH), Souris de lignée BALB C (MeSH), Spécificité d'organe (MeSH), Épithélium (métabolisme).
- MESH :
- biosynthèse : ARN messager, Protéines de transport.
- génétique : Protéines de transport.
- métabolisme : Épithélium.
- Animaux, Cellules COS, Humains, Lignée cellulaire tumorale, Protein-disulfide reductase (glutathione), Souris, Souris de lignée BALB C, Spécificité d'organe.
English descriptors
- KwdEn :
- Animals (MeSH), COS Cells (MeSH), Carrier Proteins (biosynthesis), Carrier Proteins (genetics), Cell Line, Tumor (MeSH), Chlorocebus aethiops (MeSH), Epithelium (metabolism), Humans (MeSH), Mice (MeSH), Mice, Inbred BALB C (MeSH), Organ Specificity (MeSH), Protein Disulfide Reductase (Glutathione) (MeSH), RNA, Messenger (biosynthesis).
- MESH :
- chemical , biosynthesis : Carrier Proteins, RNA, Messenger.
- chemical , genetics : Carrier Proteins.
- metabolism : Epithelium.
- Animals, COS Cells, Cell Line, Tumor, Chlorocebus aethiops, Humans, Mice, Mice, Inbred BALB C, Organ Specificity, Protein Disulfide Reductase (Glutathione).
Abstract
The protein kinase C-interacting cousin of thioredoxin (PICOT; also termed glutaredoxin 3) protein was discovered a decade ago as a protein kinase C theta (PKCtheta)-binding protein in human T lymphocytes. PICOT possesses an amino-terminal monothiol thioredoxin-like domain and a carboxy-terminal tandem repeat of a monothiol glutaredoxin-like domain. Nevertheless, the enzymatic activities of PICOT and its potential substrates have not yet been characterized and its biological importance is unknown. Earlier studies reported the presence of PICOT in several different cell lines and tissues, but its expression pattern has not been thoroughly investigated. We performed Northern blot analysis of 19 different human organs and tissues and found the expression of PICOT mRNA in all organs and tissues tested. Western blot analysis confirmed the expression of PICOT at the protein level in all organs and tissues tested and showed, in addition, that PICOT and PKCtheta expression in different tissues only partially overlap. These findings support the involvement of PICOT in biological functions that are independent of PKCtheta. To analyze the in vivo expression pattern of PICOT within cells of different human organs, we performed immunohistochemical staining using PICOT-specific antibodies. Analysis of breast, pituitary, adrenal, pancreas, and kidney sections demonstrated a differential expression of PICOT in various cell types, with a predominant cytosolic staining of epithelial cells and low or undetectable levels of PICOT in the stroma.
DOI: 10.1369/jhc.2010.956532
PubMed: 20498481
PubMed Central: PMC2924796
Affiliations:
Links toward previous steps (curation, corpus...)
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first="Moran" last="Galperin">Moran Galperin</name></author><author><name sortKey="Altman, Amnon" sort="Altman, Amnon" uniqKey="Altman A" first="Amnon" last="Altman">Amnon Altman</name></author><author><name sortKey="Isakov, Noah" sort="Isakov, Noah" uniqKey="Isakov N" first="Noah" last="Isakov">Noah Isakov</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2010">2010</date><idno type="RBID">pubmed:20498481</idno><idno type="pmid">20498481</idno><idno type="doi">10.1369/jhc.2010.956532</idno><idno type="pmc">PMC2924796</idno><idno type="wicri:Area/Main/Corpus">000A08</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000A08</idno><idno type="wicri:Area/Main/Curation">000A08</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000A08</idno><idno type="wicri:Area/Main/Exploration">000A08</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Widespread expression of PICOT in mouse and human tissues with predominant localization to epithelium.</title><author><name sortKey="Ohayon, Ariel" sort="Ohayon, Ariel" uniqKey="Ohayon A" first="Ariel" last="Ohayon">Ariel Ohayon</name><affiliation wicri:level="1"><nlm:affiliation>Shraga Segal Department of Microbiology and Immunology, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.</nlm:affiliation><country xml:lang="fr">Israël</country><wicri:regionArea>Shraga Segal Department of Microbiology and Immunology, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva</wicri:regionArea><wicri:noRegion>Beer Sheva</wicri:noRegion></affiliation></author><author><name sortKey="Babichev, Yael" sort="Babichev, Yael" uniqKey="Babichev Y" first="Yael" last="Babichev">Yael Babichev</name></author><author><name sortKey="Galperin, Moran" sort="Galperin, Moran" uniqKey="Galperin M" first="Moran" last="Galperin">Moran Galperin</name></author><author><name sortKey="Altman, Amnon" sort="Altman, Amnon" uniqKey="Altman A" first="Amnon" last="Altman">Amnon Altman</name></author><author><name sortKey="Isakov, Noah" sort="Isakov, Noah" uniqKey="Isakov N" first="Noah" last="Isakov">Noah Isakov</name></author></analytic><series><title level="j">The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society</title><idno type="eISSN">1551-5044</idno><imprint><date when="2010" type="published">2010</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals (MeSH)</term><term>COS Cells (MeSH)</term><term>Carrier Proteins (biosynthesis)</term><term>Carrier Proteins (genetics)</term><term>Cell Line, Tumor (MeSH)</term><term>Chlorocebus aethiops (MeSH)</term><term>Epithelium (metabolism)</term><term>Humans (MeSH)</term><term>Mice (MeSH)</term><term>Mice, Inbred BALB C (MeSH)</term><term>Organ Specificity (MeSH)</term><term>Protein Disulfide Reductase (Glutathione) (MeSH)</term><term>RNA, Messenger (biosynthesis)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>ARN messager (biosynthèse)</term><term>Animaux (MeSH)</term><term>Cellules COS (MeSH)</term><term>Humains (MeSH)</term><term>Lignée cellulaire tumorale (MeSH)</term><term>Protein-disulfide reductase (glutathione) (MeSH)</term><term>Protéines de transport (biosynthèse)</term><term>Protéines de transport (génétique)</term><term>Souris (MeSH)</term><term>Souris de lignée BALB C (MeSH)</term><term>Spécificité d'organe (MeSH)</term><term>Épithélium (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Carrier Proteins</term><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Carrier Proteins</term></keywords><keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>ARN messager</term><term>Protéines de transport</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Protéines de transport</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Epithelium</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Épithélium</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>COS Cells</term><term>Cell Line, Tumor</term><term>Chlorocebus aethiops</term><term>Humans</term><term>Mice</term><term>Mice, Inbred BALB C</term><term>Organ Specificity</term><term>Protein Disulfide Reductase (Glutathione)</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Cellules COS</term><term>Humains</term><term>Lignée cellulaire tumorale</term><term>Protein-disulfide reductase (glutathione)</term><term>Souris</term><term>Souris de lignée BALB C</term><term>Spécificité d'organe</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The protein kinase C-interacting cousin of thioredoxin (PICOT; also termed glutaredoxin 3) protein was discovered a decade ago as a protein kinase C theta (PKCtheta)-binding protein in human T lymphocytes. PICOT possesses an amino-terminal monothiol thioredoxin-like domain and a carboxy-terminal tandem repeat of a monothiol glutaredoxin-like domain. Nevertheless, the enzymatic activities of PICOT and its potential substrates have not yet been characterized and its biological importance is unknown. Earlier studies reported the presence of PICOT in several different cell lines and tissues, but its expression pattern has not been thoroughly investigated. We performed Northern blot analysis of 19 different human organs and tissues and found the expression of PICOT mRNA in all organs and tissues tested. Western blot analysis confirmed the expression of PICOT at the protein level in all organs and tissues tested and showed, in addition, that PICOT and PKCtheta expression in different tissues only partially overlap. These findings support the involvement of PICOT in biological functions that are independent of PKCtheta. To analyze the in vivo expression pattern of PICOT within cells of different human organs, we performed immunohistochemical staining using PICOT-specific antibodies. Analysis of breast, pituitary, adrenal, pancreas, and kidney sections demonstrated a differential expression of PICOT in various cell types, with a predominant cytosolic staining of epithelial cells and low or undetectable levels of PICOT in the stroma.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20498481</PMID><DateCompleted><Year>2010</Year><Month>09</Month><Day>02</Day></DateCompleted><DateRevised><Year>2019</Year><Month>12</Month><Day>10</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1551-5044</ISSN><JournalIssue CitedMedium="Internet"><Volume>58</Volume><Issue>9</Issue><PubDate><Year>2010</Year><Month>Sep</Month></PubDate></JournalIssue><Title>The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society</Title><ISOAbbreviation>J Histochem Cytochem</ISOAbbreviation></Journal><ArticleTitle>Widespread expression of PICOT in mouse and human tissues with predominant localization to epithelium.</ArticleTitle><Pagination><MedlinePgn>799-806</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1369/jhc.2010.956532</ELocationID><Abstract><AbstractText>The protein kinase C-interacting cousin of thioredoxin (PICOT; also termed glutaredoxin 3) protein was discovered a decade ago as a protein kinase C theta (PKCtheta)-binding protein in human T lymphocytes. PICOT possesses an amino-terminal monothiol thioredoxin-like domain and a carboxy-terminal tandem repeat of a monothiol glutaredoxin-like domain. Nevertheless, the enzymatic activities of PICOT and its potential substrates have not yet been characterized and its biological importance is unknown. Earlier studies reported the presence of PICOT in several different cell lines and tissues, but its expression pattern has not been thoroughly investigated. We performed Northern blot analysis of 19 different human organs and tissues and found the expression of PICOT mRNA in all organs and tissues tested. Western blot analysis confirmed the expression of PICOT at the protein level in all organs and tissues tested and showed, in addition, that PICOT and PKCtheta expression in different tissues only partially overlap. These findings support the involvement of PICOT in biological functions that are independent of PKCtheta. To analyze the in vivo expression pattern of PICOT within cells of different human organs, we performed immunohistochemical staining using PICOT-specific antibodies. Analysis of breast, pituitary, adrenal, pancreas, and kidney sections demonstrated a differential expression of PICOT in various cell types, with a predominant cytosolic staining of epithelial cells and low or undetectable levels of PICOT in the stroma.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ohayon</LastName><ForeName>Ariel</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>Shraga Segal Department of Microbiology and Immunology, Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Babichev</LastName><ForeName>Yael</ForeName><Initials>Y</Initials></Author><Author ValidYN="Y"><LastName>Galperin</LastName><ForeName>Moran</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Altman</LastName><ForeName>Amnon</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Isakov</LastName><ForeName>Noah</ForeName><Initials>N</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2010</Year><Month>05</Month><Day>24</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>J Histochem Cytochem</MedlineTA><NlmUniqueID>9815334</NlmUniqueID><ISSNLinking>0022-1554</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D002352">Carrier Proteins</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="C404105">GLRX3 protein, human</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.8.4.2</RegistryNumber><NameOfSubstance UI="D011490">Protein Disulfide Reductase (Glutathione)</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.8.4.2</RegistryNumber><NameOfSubstance UI="C498606">Txnl2 protein, mouse</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019556" MajorTopicYN="N">COS Cells</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002352" MajorTopicYN="N">Carrier Proteins</DescriptorName><QualifierName UI="Q000096" MajorTopicYN="Y">biosynthesis</QualifierName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D045744" MajorTopicYN="N">Cell Line, Tumor</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002522" MajorTopicYN="N">Chlorocebus aethiops</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D004848" MajorTopicYN="N">Epithelium</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008807" MajorTopicYN="N">Mice, Inbred BALB C</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D009928" MajorTopicYN="N">Organ Specificity</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D011490" MajorTopicYN="N">Protein Disulfide Reductase (Glutathione)</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName><QualifierName UI="Q000096" 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