Redox atlas of the mouse. Immunohistochemical detection of glutaredoxin-, peroxiredoxin-, and thioredoxin-family proteins in various tissues of the laboratory mouse.
Identifieur interne : 000926 ( Main/Exploration ); précédent : 000925; suivant : 000927Redox atlas of the mouse. Immunohistochemical detection of glutaredoxin-, peroxiredoxin-, and thioredoxin-family proteins in various tissues of the laboratory mouse.
Auteurs : José Rodrigo Godoy [Allemagne] ; Maria Funke ; Waltraud Ackermann ; Petra Haunhorst ; Sabrina Oesteritz ; Francisco Capani ; Hans-Peter Els Sser ; Christopher Horst LilligSource :
- Biochimica et biophysica acta [ 0006-3002 ] ; 2011.
Descripteurs français
- KwdFr :
- Animaux (MeSH), Atlas comme sujet (MeSH), Distribution tissulaire (MeSH), Femelle (MeSH), Glutarédoxines (génétique), Glutarédoxines (immunologie), Glutarédoxines (métabolisme), Grossesse (MeSH), Humains (MeSH), Immunohistochimie (MeSH), Modèles biologiques (MeSH), Mâle (MeSH), Oxydoréduction (MeSH), Peroxirédoxines (génétique), Peroxirédoxines (immunologie), Peroxirédoxines (métabolisme), Souris (génétique), Souris (immunologie), Souris (métabolisme), Thiorédoxines (génétique), Thiorédoxines (immunologie), Thiorédoxines (métabolisme).
- MESH :
- génétique : Glutarédoxines, Peroxirédoxines, Souris, Thiorédoxines.
- immunologie : Glutarédoxines, Peroxirédoxines, Souris, Thiorédoxines.
- métabolisme : Glutarédoxines, Peroxirédoxines, Souris, Thiorédoxines.
- Animaux, Atlas comme sujet, Distribution tissulaire, Femelle, Grossesse, Humains, Immunohistochimie, Modèles biologiques, Mâle, Oxydoréduction.
English descriptors
- KwdEn :
- Animals (MeSH), Atlases as Topic (MeSH), Female (MeSH), Glutaredoxins (genetics), Glutaredoxins (immunology), Glutaredoxins (metabolism), Humans (MeSH), Immunohistochemistry (MeSH), Male (MeSH), Mice (genetics), Mice (immunology), Mice (metabolism), Models, Biological (MeSH), Oxidation-Reduction (MeSH), Peroxiredoxins (genetics), Peroxiredoxins (immunology), Peroxiredoxins (metabolism), Pregnancy (MeSH), Thioredoxins (genetics), Thioredoxins (immunology), Thioredoxins (metabolism), Tissue Distribution (MeSH).
- MESH :
- chemical , genetics : Glutaredoxins, Peroxiredoxins, Thioredoxins.
- chemical , immunology : Glutaredoxins, Peroxiredoxins, Thioredoxins.
- chemical , metabolism : Glutaredoxins, Peroxiredoxins, Thioredoxins.
- genetics : Mice.
- immunology : Mice.
- metabolism : Mice.
- Animals, Atlases as Topic, Female, Humans, Immunohistochemistry, Male, Models, Biological, Oxidation-Reduction, Pregnancy, Tissue Distribution.
Abstract
BACKGROUND
Oxidoreductases of the thioredoxin family of proteins have been thoroughly studied in numerous cellular and animal models mimicking human diseases. Despite of their well documented role in various disease conditions, no systematic information on the presence of these proteins is available.
METHODS
Here, we have systematically analyzed the presence of some of the major constituents of the glutaredoxin (Grx)-, peroxiredoxin (Prx)-, and thioredoxin (Trx)-systems, i.e. Grx1, Grx2, Grx3 (TXNL-2/PICOT), Grx5, nucleoredoxin (Nrx), Prx1, Prx2, Prx3, Prx4, Prx5, Prx6, Trx1, thioredoxin reductase 1 (TrxR1), Trx2, TrxR2, and γ-glutamyl cysteine synthetase (γ-GCS) in various tissues of the mouse using immunohistochemistry.
RESULTS
The identification of the Trx family proteins in the central nervous system, sensory organs, digestive system, lymphatic system, reproductive system, urinary system, respiratory system, endocrine system, skin, heart, and muscle revealed a number of significant differences between these proteins with respect to their distribution in these tissues.
CONCLUSION
Our results imply more specific functions and interactions between the proteins of this family than previously assumed.
GENERAL SIGNIFICANCE
Crucial functions of Trx family proteins have been demonstrated in various disease conditions. A detailed overview on their distribution in various tissues will be helpful to fully comprehend their potential role and the interactions of these proteins in the most thoroughly studied model for human diseases-the laboratory mouse. This article is part of a Special Issue entitled Human and Murine Redox Protein Atlases.
DOI: 10.1016/j.bbagen.2010.05.006
PubMed: 20682242
Affiliations:
Links toward previous steps (curation, corpus...)
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Immunohistochemical detection of glutaredoxin-, peroxiredoxin-, and thioredoxin-family proteins in various tissues of the laboratory mouse.</title><author><name sortKey="Godoy, Jose Rodrigo" sort="Godoy, Jose Rodrigo" uniqKey="Godoy J" first="José Rodrigo" last="Godoy">José Rodrigo Godoy</name><affiliation wicri:level="3"><nlm:affiliation>Institut für Klinische Zytobiologie und Zytopathologie, Fachbereich Medizin, Philipps Universität, Marburg, Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institut für Klinische Zytobiologie und Zytopathologie, Fachbereich Medizin, Philipps Universität, Marburg</wicri:regionArea><placeName><region type="land" nuts="1">Hesse (Land)</region><region type="district" nuts="2">District de Giessen</region><settlement type="city">Marbourg</settlement></placeName></affiliation></author><author><name sortKey="Funke, Maria" sort="Funke, Maria" uniqKey="Funke M" first="Maria" last="Funke">Maria Funke</name></author><author><name sortKey="Ackermann, Waltraud" sort="Ackermann, Waltraud" uniqKey="Ackermann W" first="Waltraud" last="Ackermann">Waltraud Ackermann</name></author><author><name sortKey="Haunhorst, Petra" sort="Haunhorst, Petra" uniqKey="Haunhorst P" first="Petra" last="Haunhorst">Petra Haunhorst</name></author><author><name sortKey="Oesteritz, Sabrina" sort="Oesteritz, Sabrina" uniqKey="Oesteritz S" first="Sabrina" last="Oesteritz">Sabrina Oesteritz</name></author><author><name sortKey="Capani, Francisco" sort="Capani, Francisco" uniqKey="Capani F" first="Francisco" last="Capani">Francisco Capani</name></author><author><name sortKey="Els Sser, Hans Peter" sort="Els Sser, Hans Peter" uniqKey="Els Sser H" first="Hans-Peter" last="Els Sser">Hans-Peter Els Sser</name></author><author><name sortKey="Lillig, Christopher Horst" sort="Lillig, Christopher Horst" uniqKey="Lillig C" first="Christopher Horst" last="Lillig">Christopher Horst Lillig</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2011">2011</date><idno type="RBID">pubmed:20682242</idno><idno type="pmid">20682242</idno><idno type="doi">10.1016/j.bbagen.2010.05.006</idno><idno type="wicri:Area/Main/Corpus">000983</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000983</idno><idno type="wicri:Area/Main/Curation">000983</idno><idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Curation">000983</idno><idno type="wicri:Area/Main/Exploration">000983</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Redox atlas of the mouse. Immunohistochemical detection of glutaredoxin-, peroxiredoxin-, and thioredoxin-family proteins in various tissues of the laboratory mouse.</title><author><name sortKey="Godoy, Jose Rodrigo" sort="Godoy, Jose Rodrigo" uniqKey="Godoy J" first="José Rodrigo" last="Godoy">José Rodrigo Godoy</name><affiliation wicri:level="3"><nlm:affiliation>Institut für Klinische Zytobiologie und Zytopathologie, Fachbereich Medizin, Philipps Universität, Marburg, Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Institut für Klinische Zytobiologie und Zytopathologie, Fachbereich Medizin, Philipps Universität, Marburg</wicri:regionArea><placeName><region type="land" nuts="1">Hesse (Land)</region><region type="district" nuts="2">District de Giessen</region><settlement type="city">Marbourg</settlement></placeName></affiliation></author><author><name sortKey="Funke, Maria" sort="Funke, Maria" uniqKey="Funke M" first="Maria" last="Funke">Maria Funke</name></author><author><name sortKey="Ackermann, Waltraud" sort="Ackermann, Waltraud" uniqKey="Ackermann W" first="Waltraud" last="Ackermann">Waltraud Ackermann</name></author><author><name sortKey="Haunhorst, Petra" sort="Haunhorst, Petra" uniqKey="Haunhorst P" first="Petra" last="Haunhorst">Petra Haunhorst</name></author><author><name sortKey="Oesteritz, Sabrina" sort="Oesteritz, Sabrina" uniqKey="Oesteritz S" first="Sabrina" last="Oesteritz">Sabrina Oesteritz</name></author><author><name sortKey="Capani, Francisco" sort="Capani, Francisco" uniqKey="Capani F" first="Francisco" last="Capani">Francisco Capani</name></author><author><name sortKey="Els Sser, Hans Peter" sort="Els Sser, Hans Peter" uniqKey="Els Sser H" first="Hans-Peter" last="Els Sser">Hans-Peter Els Sser</name></author><author><name sortKey="Lillig, Christopher Horst" sort="Lillig, Christopher Horst" uniqKey="Lillig C" first="Christopher Horst" last="Lillig">Christopher Horst Lillig</name></author></analytic><series><title level="j">Biochimica et biophysica acta</title><idno type="ISSN">0006-3002</idno><imprint><date when="2011" type="published">2011</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals (MeSH)</term><term>Atlases as Topic (MeSH)</term><term>Female (MeSH)</term><term>Glutaredoxins (genetics)</term><term>Glutaredoxins (immunology)</term><term>Glutaredoxins (metabolism)</term><term>Humans (MeSH)</term><term>Immunohistochemistry (MeSH)</term><term>Male (MeSH)</term><term>Mice (genetics)</term><term>Mice (immunology)</term><term>Mice (metabolism)</term><term>Models, Biological (MeSH)</term><term>Oxidation-Reduction (MeSH)</term><term>Peroxiredoxins (genetics)</term><term>Peroxiredoxins (immunology)</term><term>Peroxiredoxins (metabolism)</term><term>Pregnancy (MeSH)</term><term>Thioredoxins (genetics)</term><term>Thioredoxins (immunology)</term><term>Thioredoxins (metabolism)</term><term>Tissue Distribution (MeSH)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux (MeSH)</term><term>Atlas comme sujet (MeSH)</term><term>Distribution tissulaire (MeSH)</term><term>Femelle (MeSH)</term><term>Glutarédoxines (génétique)</term><term>Glutarédoxines (immunologie)</term><term>Glutarédoxines (métabolisme)</term><term>Grossesse (MeSH)</term><term>Humains (MeSH)</term><term>Immunohistochimie (MeSH)</term><term>Modèles biologiques (MeSH)</term><term>Mâle (MeSH)</term><term>Oxydoréduction (MeSH)</term><term>Peroxirédoxines (génétique)</term><term>Peroxirédoxines (immunologie)</term><term>Peroxirédoxines (métabolisme)</term><term>Souris (génétique)</term><term>Souris (immunologie)</term><term>Souris (métabolisme)</term><term>Thiorédoxines (génétique)</term><term>Thiorédoxines (immunologie)</term><term>Thiorédoxines (métabolisme)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Glutaredoxins</term><term>Peroxiredoxins</term><term>Thioredoxins</term></keywords><keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Glutaredoxins</term><term>Peroxiredoxins</term><term>Thioredoxins</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Glutaredoxins</term><term>Peroxiredoxins</term><term>Thioredoxins</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Mice</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Glutarédoxines</term><term>Peroxirédoxines</term><term>Souris</term><term>Thiorédoxines</term></keywords><keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Glutarédoxines</term><term>Peroxirédoxines</term><term>Souris</term><term>Thiorédoxines</term></keywords><keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Mice</term></keywords><keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Mice</term></keywords><keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Glutarédoxines</term><term>Peroxirédoxines</term><term>Souris</term><term>Thiorédoxines</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Atlases as Topic</term><term>Female</term><term>Humans</term><term>Immunohistochemistry</term><term>Male</term><term>Models, Biological</term><term>Oxidation-Reduction</term><term>Pregnancy</term><term>Tissue Distribution</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Atlas comme sujet</term><term>Distribution tissulaire</term><term>Femelle</term><term>Grossesse</term><term>Humains</term><term>Immunohistochimie</term><term>Modèles biologiques</term><term>Mâle</term><term>Oxydoréduction</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p><b>BACKGROUND</b></p><p>Oxidoreductases of the thioredoxin family of proteins have been thoroughly studied in numerous cellular and animal models mimicking human diseases. Despite of their well documented role in various disease conditions, no systematic information on the presence of these proteins is available.</p></div><div type="abstract" xml:lang="en"><p><b>METHODS</b></p><p>Here, we have systematically analyzed the presence of some of the major constituents of the glutaredoxin (Grx)-, peroxiredoxin (Prx)-, and thioredoxin (Trx)-systems, i.e. Grx1, Grx2, Grx3 (TXNL-2/PICOT), Grx5, nucleoredoxin (Nrx), Prx1, Prx2, Prx3, Prx4, Prx5, Prx6, Trx1, thioredoxin reductase 1 (TrxR1), Trx2, TrxR2, and γ-glutamyl cysteine synthetase (γ-GCS) in various tissues of the mouse using immunohistochemistry.</p></div><div type="abstract" xml:lang="en"><p><b>RESULTS</b></p><p>The identification of the Trx family proteins in the central nervous system, sensory organs, digestive system, lymphatic system, reproductive system, urinary system, respiratory system, endocrine system, skin, heart, and muscle revealed a number of significant differences between these proteins with respect to their distribution in these tissues.</p></div><div type="abstract" xml:lang="en"><p><b>CONCLUSION</b></p><p>Our results imply more specific functions and interactions between the proteins of this family than previously assumed.</p></div><div type="abstract" xml:lang="en"><p><b>GENERAL SIGNIFICANCE</b></p><p>Crucial functions of Trx family proteins have been demonstrated in various disease conditions. A detailed overview on their distribution in various tissues will be helpful to fully comprehend their potential role and the interactions of these proteins in the most thoroughly studied model for human diseases-the laboratory mouse. This article is part of a Special Issue entitled Human and Murine Redox Protein Atlases.</p></div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20682242</PMID><DateCompleted><Year>2011</Year><Month>02</Month><Day>16</Day></DateCompleted><DateRevised><Year>2019</Year><Month>12</Month><Day>10</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0006-3002</ISSN><JournalIssue CitedMedium="Print"><Volume>1810</Volume><Issue>1</Issue><PubDate><Year>2011</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Biochimica et biophysica acta</Title><ISOAbbreviation>Biochim Biophys Acta</ISOAbbreviation></Journal><ArticleTitle>Redox atlas of the mouse. Immunohistochemical detection of glutaredoxin-, peroxiredoxin-, and thioredoxin-family proteins in various tissues of the laboratory mouse.</ArticleTitle><Pagination><MedlinePgn>2-92</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.bbagen.2010.05.006</ELocationID><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Oxidoreductases of the thioredoxin family of proteins have been thoroughly studied in numerous cellular and animal models mimicking human diseases. Despite of their well documented role in various disease conditions, no systematic information on the presence of these proteins is available.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">Here, we have systematically analyzed the presence of some of the major constituents of the glutaredoxin (Grx)-, peroxiredoxin (Prx)-, and thioredoxin (Trx)-systems, i.e. Grx1, Grx2, Grx3 (TXNL-2/PICOT), Grx5, nucleoredoxin (Nrx), Prx1, Prx2, Prx3, Prx4, Prx5, Prx6, Trx1, thioredoxin reductase 1 (TrxR1), Trx2, TrxR2, and γ-glutamyl cysteine synthetase (γ-GCS) in various tissues of the mouse using immunohistochemistry.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">The identification of the Trx family proteins in the central nervous system, sensory organs, digestive system, lymphatic system, reproductive system, urinary system, respiratory system, endocrine system, skin, heart, and muscle revealed a number of significant differences between these proteins with respect to their distribution in these tissues.</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Our results imply more specific functions and interactions between the proteins of this family than previously assumed.</AbstractText><AbstractText Label="GENERAL SIGNIFICANCE" NlmCategory="CONCLUSIONS">Crucial functions of Trx family proteins have been demonstrated in various disease conditions. A detailed overview on their distribution in various tissues will be helpful to fully comprehend their potential role and the interactions of these proteins in the most thoroughly studied model for human diseases-the laboratory mouse. This article is part of a Special Issue entitled Human and Murine Redox Protein Atlases.</AbstractText><CopyrightInformation>Copyright © 2010 Elsevier B.V. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Godoy</LastName><ForeName>José Rodrigo</ForeName><Initials>JR</Initials><AffiliationInfo><Affiliation>Institut für Klinische Zytobiologie und Zytopathologie, Fachbereich Medizin, Philipps Universität, Marburg, Germany.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Funke</LastName><ForeName>Maria</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Ackermann</LastName><ForeName>Waltraud</ForeName><Initials>W</Initials></Author><Author ValidYN="Y"><LastName>Haunhorst</LastName><ForeName>Petra</ForeName><Initials>P</Initials></Author><Author ValidYN="Y"><LastName>Oesteritz</LastName><ForeName>Sabrina</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Capani</LastName><ForeName>Francisco</ForeName><Initials>F</Initials></Author><Author ValidYN="Y"><LastName>Elsässer</LastName><ForeName>Hans-Peter</ForeName><Initials>HP</Initials></Author><Author ValidYN="Y"><LastName>Lillig</LastName><ForeName>Christopher Horst</ForeName><Initials>CH</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType><PublicationType UI="D023361">Validation Study</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2010</Year><Month>06</Month><Day>01</Day></ArticleDate></Article><MedlineJournalInfo><Country>Netherlands</Country><MedlineTA>Biochim Biophys Acta</MedlineTA><NlmUniqueID>0217513</NlmUniqueID><ISSNLinking>0006-3002</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D054477">Glutaredoxins</NameOfSubstance></Chemical><Chemical><RegistryNumber>52500-60-4</RegistryNumber><NameOfSubstance UI="D013879">Thioredoxins</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 1.11.1.15</RegistryNumber><NameOfSubstance UI="D054464">Peroxiredoxins</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001271" MajorTopicYN="N">Atlases as Topic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D054477" MajorTopicYN="N">Glutaredoxins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007150" MajorTopicYN="N">Immunohistochemistry</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008954" MajorTopicYN="N">Models, Biological</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010084" MajorTopicYN="N">Oxidation-Reduction</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D054464" MajorTopicYN="N">Peroxiredoxins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011247" MajorTopicYN="N">Pregnancy</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013879" MajorTopicYN="N">Thioredoxins</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName><QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014018" MajorTopicYN="N">Tissue Distribution</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2010</Year><Month>04</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2010</Year><Month>05</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2010</Year><Month>05</Month><Day>14</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2010</Year><Month>8</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2010</Year><Month>8</Month><Day>5</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2011</Year><Month>2</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">20682242</ArticleId><ArticleId IdType="pii">S0304-4165(10)00139-X</ArticleId><ArticleId IdType="doi">10.1016/j.bbagen.2010.05.006</ArticleId></ArticleIdList></PubmedData></pubmed><affiliations><list><country><li>Allemagne</li></country><region><li>District de Giessen</li><li>Hesse (Land)</li></region><settlement><li>Marbourg</li></settlement></list><tree><noCountry><name sortKey="Ackermann, Waltraud" sort="Ackermann, Waltraud" uniqKey="Ackermann W" first="Waltraud" last="Ackermann">Waltraud Ackermann</name><name sortKey="Capani, Francisco" sort="Capani, Francisco" uniqKey="Capani F" first="Francisco" last="Capani">Francisco Capani</name><name sortKey="Els Sser, Hans Peter" sort="Els Sser, Hans Peter" uniqKey="Els Sser H" first="Hans-Peter" last="Els Sser">Hans-Peter Els Sser</name><name sortKey="Funke, Maria" sort="Funke, Maria" uniqKey="Funke M" first="Maria" last="Funke">Maria Funke</name><name sortKey="Haunhorst, Petra" sort="Haunhorst, Petra" uniqKey="Haunhorst P" first="Petra" last="Haunhorst">Petra Haunhorst</name><name sortKey="Lillig, Christopher Horst" sort="Lillig, Christopher Horst" uniqKey="Lillig C" first="Christopher Horst" last="Lillig">Christopher Horst Lillig</name><name sortKey="Oesteritz, Sabrina" sort="Oesteritz, Sabrina" uniqKey="Oesteritz S" first="Sabrina" last="Oesteritz">Sabrina Oesteritz</name></noCountry><country name="Allemagne"><region name="Hesse (Land)"><name sortKey="Godoy, Jose Rodrigo" sort="Godoy, Jose Rodrigo" uniqKey="Godoy J" first="José Rodrigo" 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