Publication:
A chemokine targets the nucleus: Cxcl12-gamma isoform localizes to the nucleolus in adult mouse heart.

dc.contributor.authorTorres, Raul
dc.contributor.authorRamirez, Juan C
dc.contributor.funderMinisterio de Sanidad y Consumo (España)
dc.contributor.funderFundación Mutua Madrileña
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderFundación ProCNIC
dc.date.accessioned2025-01-27T14:14:20Z
dc.date.available2025-01-27T14:14:20Z
dc.date.issued2009-10-27
dc.descriptionR.T. is supported by a contract from the Ministry of Health and Consumer Affairs. This study was supported by a grant of the Ministry of Health and Custom affairs (FIS 06/0911) (www.msyc.es; http://www.isciii.es) and funding from the Fundacio´n Mutua Madrilen˜ a (www.mutua-mad.es/FundMM/jsp/Fhome. jsp)(2005/084) to J.C.R. The CNIC is supported by the Ministry of Science and Innovation and the Pro-CNIC Foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
dc.description.abstractChemokines are extracellular mediators of complex regulatory circuits involved principally in cell-to-cell communication. Most studies to date of the essential chemokine Cxcl12 (Sdf-1) have focused on the ubiquitously expressed secreted isoforms alpha and beta. Here we show that, unlike these isoforms and all other known chemokines, the alternatively transcribed gamma isoform is an intracellular protein that localizes to the nucleolus in differentiated mouse Cardiac tissue. Our results demonstrate that nucleolar transportation is encoded by a nucleolar-localization signal in the unique carboxy-terminal region of Sdf-1gamma, and is competent both in vivo and in vitro. The molecular mechanism underlying these unusual chemokine properties involves cardiac-specific transcription of an mRNA containing a unique short-leader sequence lacking the signal peptide and translation from a non-canonical CUG codon. Our results provide an example of genome economy even for essential and highly conserved genes such as Cxcl12, and suggest that chemokines can exert tissue specific functions unrelated to cell-to-cell communication.
dc.description.peerreviewed
dc.format.number(10)
dc.format.pagee7570
dc.format.volume4
dc.identifier.citationPLoS One. 2009 Oct 27;4(10):e7570.
dc.identifier.journalPLoS One
dc.identifier.pubmedID19859557
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26153
dc.language.isoeng
dc.publisherPublic Library of Science (PLOS)
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/FIS/06/0911
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/2005/084
dc.relation.publisherversionhttps://10.1371/journal.pone.0007570
dc.repisalud.institucionCNIC
dc.repisalud.orgCNICCNIC::Unidades técnicas::Vectores Virales
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleA chemokine targets the nucleus: Cxcl12-gamma isoform localizes to the nucleolus in adult mouse heart.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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