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dc.contributor.authorMatamala, Nerea 
dc.contributor.authorAggarwal, Nupur
dc.contributor.authorIadarola, Paolo
dc.contributor.authorFumagalli, Marco
dc.contributor.authorGomez-Mariano, Gema Maria 
dc.contributor.authorLara, Beatriz
dc.contributor.authorVarela Martinez, Maria del Carmen 
dc.contributor.authorCuesta, Isabel 
dc.contributor.authorStolk, Jan
dc.contributor.authorJanciauskiene, Sabina
dc.contributor.authorMartinez-Delgado, Beatriz 
dc.date.accessioned2018-10-09T17:16:32Z
dc.date.available2018-10-09T17:16:32Z
dc.date.issued2017
dc.identifier.citationPLoS One. 2017 Jan 20;12(1):e0170533.es_ES
dc.identifier.issn1932-6203es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/6488
dc.description.abstractHuman SERPINA1 gene is located on chromosome 14q31-32.3 and is organized into three (IA, IB, and IC) non-coding and four (II, III, IV, V) coding exons. This gene produces α1-antitrypsin (A1AT), a prototypical member of the serpin superfamily of proteins. We demonstrate that human peripheral blood leukocytes express not only a product corresponding to the transcript coding for the full-length A1AT protein but also two short transcripts (ST1C4 and ST1C5) of A1AT. In silico sequence analysis revealed that the last exon of the short transcripts contains an Open Reading Frame (ORF) and thus putatively can produce peptides. We found ST1C4 expression across different human tissues whereas ST1C5 was mainly restricted to leukocytes, specifically neutrophils. A high up-regulation (10-fold) of short transcripts was observed in isolated human blood neutrophils after activation with lipopolysaccharide. Parallel analyses by liquid chromatography-mass spectrometry identified peptides corresponding to C-terminal region of A1AT in supernatants of activated but not naïve neutrophils. Herein we report for the first time a tissue specific expression and regulation of short transcripts of SERPINA1 gene, and the presence of C-terminal peptides in supernatants from activated neutrophils, in vitro. This gives a novel insight into the studies on the transcription of SERPINA1 gene.es_ES
dc.description.sponsorshipThis work has been partially funded by the Instituto de Salud Carlos III (www.isciii.es) grant PI14CIII/00070 (BMD) and SEPAR (Sociedad Española de Neumología y Cirugía Torácica, www.separ.es) grant 92/2014. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es_ES
dc.language.isoenges_ES
dc.publisherPublic Library of Sciencees_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshComputer Simulation es_ES
dc.subject.meshGene Expression Regulation es_ES
dc.subject.meshHumans es_ES
dc.subject.meshIn Vitro Techniques es_ES
dc.subject.meshLeukocytes es_ES
dc.subject.meshLeukocytes, Mononuclear es_ES
dc.subject.meshLipopolysaccharides es_ES
dc.subject.meshNeutrophils es_ES
dc.subject.meshOpen Reading Frames es_ES
dc.subject.meshPolymerase Chain Reaction es_ES
dc.subject.meshalpha 1-Antitrypsin es_ES
dc.titleIdentification of Novel Short C-Terminal Transcripts of Human SERPINA1 Genees_ES
dc.typeArtículoes_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID28107454es_ES
dc.format.volume12es_ES
dc.format.number1es_ES
dc.format.pagee0170533es_ES
dc.identifier.doi10.1371/journal.pone.0170533es_ES
dc.contributor.funderInstituto de Salud Carlos III - ISCIII
dc.contributor.funderSociedad Española de Neumología y Cirugía Torácica
dc.description.peerreviewedes_ES
dc.identifier.e-issn1932-6203es_ES
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0170533es_ES
dc.identifier.journalPloS onees_ES
dc.repisalud.centroISCIII::Instituto de Investigación de Enfermedades Rarases_ES
dc.repisalud.institucionISCIIIes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PI14CIII/00070es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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Atribución 4.0 Internacional
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