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dc.contributor.authorSwaminathan, Bhairavi
dc.contributor.authorThorleifsson, Gudmar
dc.contributor.authorJöud, Magnus
dc.contributor.authorAli, Mina
dc.contributor.authorJohnsson, Ellinor
dc.contributor.authorAjore, Ram
dc.contributor.authorSulem, Patrick
dc.contributor.authorHalvarsson, Britt-Marie
dc.contributor.authorEyjolfsson, Gudmundur I.
dc.contributor.authorHaraldsdottir, Vilhelmina
dc.contributor.authorHultman, Christina
dc.contributor.authorIngelsson, Erik
dc.contributor.authorKristinsson, Sigurdur Y
dc.contributor.authorKähler, Anna Katarina
dc.contributor.authorLenhoff, Stig
dc.contributor.authorMasson, Gisli
dc.contributor.authorMellqvist, Ulf-Henrik
dc.contributor.authorMånsson, Robert
dc.contributor.authorNelander, Sven
dc.contributor.authorOlafsson, Isleifur
dc.contributor.authorSigurdardóttir, Olöf Gudrun
dc.contributor.authorSteingrimsdottir, Hlif
dc.contributor.authorVangsted, Annette
dc.contributor.authorVogel, Ulla
dc.contributor.authorWaage, Anders
dc.contributor.authorNahi, Hareth
dc.contributor.authorGudbjartsson, Daniel F.
dc.contributor.authorRafnar, Thorunn
dc.contributor.authorTuresson, Ingemar
dc.contributor.authorGullberg, Urban
dc.contributor.authorStefansson, Kari
dc.contributor.authorHansson, Markus
dc.contributor.authorThorsteinsdottir, Unnur
dc.contributor.authorNilsson, Björn
dc.date.accessioned2015-09-29T12:07:21Z
dc.date.accessioned2015-10-20T09:29:53Z
dc.date.available2015-09-29T12:07:21Z
dc.date.available2015-10-20T09:29:53Z
dc.date.issued2015
dc.identifier.citationNature Communications 2015, 6nb_NO
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/11250/2357182
dc.description.abstractMultiple myeloma (MM) is characterized by an uninhibited, clonal growth of plasma cells. While first-degree relatives of patients with MM show an increased risk of MM, the genetic basis of inherited MM susceptibility is incompletely understood. Here we report a genomewide association study in the Nordic region identifying a novel MM risk locus at ELL2 (rs56219066T; odds ratio (OR)=1.25; P=9.6 x10 -10). This gene encodes a stoichiometrically limiting component of the super-elongation complex that drives secretory-specific immunoglobulin mRNA production and transcriptional regulation in plasma cells.We find that the MM risk allele harbours a Thr298Ala missense variant in an ELL2 domain required for transcription elongation. Consistent with a hypomorphic effect, we find that the MM risk allele also associates with reduced levels of immunoglobulin A (IgA) and G (IgG) in healthy subjects (P=8.6x 10- 9 and P=6.4x 10- 3, respectively) and, potentially, with an increased risk of bacterial meningitis (OR=1.30; P=0.0024).nb_NO
dc.language.isoengnb_NO
dc.publisherNature Publishing Groupnb_NO
dc.titleVariants in ELL2 influencing immunoglobulin levels associate with multiple myelomanb_NO
dc.typeJournal articlenb_NO
dc.typePeer revieweden_GB
dc.date.updated2015-09-29T12:07:21Z
dc.source.volume6nb_NO
dc.source.journalNature Communicationsnb_NO
dc.identifier.doi10.1038/ncomms8213
dc.identifier.cristin1257321
dc.description.localcode(c)2015 Macmillan Publishers Limited. All rights reserved. Creative Commons Attribution License 4.0.nb_NO


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