Author
Listed:
- Mina Ali
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Ram Ajore
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Anna-Karin Wihlborg
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Abhishek Niroula
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Bhairavi Swaminathan
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Ellinor Johnsson
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Owen W Stephens
(University of Arkansas for Medical Sciences)
- Gareth Morgan
(University of Arkansas for Medical Sciences)
- Tobias Meissner
(Department of Molecular and Experimental Medicine, Avera Cancer Institute)
- Ingemar Turesson
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Hartmut Goldschmidt
(University of Heidelberg
National Center for Tumor Diseases)
- Ulf-Henrik Mellqvist
(South Elvsborg Hospital)
- Urban Gullberg
(Department of Laboratory Medicine, Hematology and Transfusion Medicine)
- Markus Hansson
(Department of Laboratory Medicine, Hematology and Transfusion Medicine
Skåne University Hospital)
- Kari Hemminki
(German Cancer Research Center
Lund University)
- Hareth Nahi
(Karolinska Institutet)
- Anders Waage
(Norwegian University of Science and Technology)
- Niels Weinhold
(University of Arkansas for Medical Sciences)
- Björn Nilsson
(Department of Laboratory Medicine, Hematology and Transfusion Medicine
Broad Institute)
Abstract
Recently, we identified ELL2 as a susceptibility gene for multiple myeloma (MM). To understand its mechanism of action, we performed expression quantitative trait locus analysis in CD138+ plasma cells from 1630 MM patients from four populations. We show that the MM risk allele lowers ELL2 expression in these cells (Pcombined = 2.5 × 10−27; βcombined = −0.24 SD), but not in peripheral blood or other tissues. Consistent with this, several variants representing the MM risk allele map to regulatory genomic regions, and three yield reduced transcriptional activity in plasmocytoma cell lines. One of these (rs3777189-C) co-locates with the best-supported lead variants for ELL2 expression and MM risk, and reduces binding of MAFF/G/K family transcription factors. Moreover, further analysis reveals that the MM risk allele associates with upregulation of gene sets related to ribosome biogenesis, and knockout/knockdown and rescue experiments in plasmocytoma cell lines support a cause–effect relationship. Our results provide mechanistic insight into MM predisposition.
Suggested Citation
Mina Ali & Ram Ajore & Anna-Karin Wihlborg & Abhishek Niroula & Bhairavi Swaminathan & Ellinor Johnsson & Owen W Stephens & Gareth Morgan & Tobias Meissner & Ingemar Turesson & Hartmut Goldschmidt & U, 2018.
"The multiple myeloma risk allele at 5q15 lowers ELL2 expression and increases ribosomal gene expression,"
Nature Communications, Nature, vol. 9(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-04082-2
DOI: 10.1038/s41467-018-04082-2
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