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A novel TNFRSF1A splice mutation associated with increased NF-κB transcription factor activation in patients with TNF-receptor associated periodic syndrome (TRAPS)
  1. Sarah M Churchman (s.m.churchman{at}leeds.ac.uk)
  1. Leeds Institute of Molecular Medicine, United Kingdom
    1. Leigh D Church (l.church{at}leeds.ac.uk)
    1. Leeds Institute of Molecular Medicine, United Kingdom
      1. Sinisa Savic (sinisa{at}doctors.org.uk)
      1. Leeds Institute of Molecular Medicine, United Kingdom
        1. Lydia R Coulthard (ugmlrc{at}leeds.ac.uk)
        1. Leeds Institute of Molecular Medicine, United Kingdom
          1. Bruce Hayward (medbha{at}leeds.ac.uk)
          1. Leeds Institute of Molecular Medicine, United Kingdom
            1. Belinda Nedjai (b.nedjai{at}qmul.ac.uk)
            1. Centre for Diabetes and Metabolic Medicine, United Kingdom
              1. Mark D. Turner (m.d.turner{at}qmul.ac.uk)
              1. Centre for Diabetes and Metabolic Medicine, United Kingdom
                1. Rebeccah J. Mathews (ugmrjm{at}leeds.ac.uk)
                1. Leeds Institute of Molecular Medicine, United Kingdom
                  1. Elaine Baguley (elaine.baguley{at}hey.nhs.uk)
                  1. Department of Rheumatology, Hull Royal Infirmary, United Kingdom
                    1. Graham A. Hitman (g.a.hitman{at}qmul.ac.uk)
                    1. Centre for Diabetes and Metabolic Medicine, United Kingdom
                      1. Hock C. Gooi (jimmy.gooi{at}leedsth.nhs.uk)
                      1. Department of Clinical Immunology and Allergy, St. James’s University Hospital, Leeds, United Kingdom
                        1. Philip Wood (p.wood{at}leedsth.nhs.uk)
                        1. Department of Clinical Immunology and Allergy, St. James’s University Hospital, Leeds, United Kingdom
                          1. Paul Emery (p.emery{at}leeds.ac.uk)
                          1. Dept of Rheumatology,, United Kingdom
                            1. Micheal F. McDermott (m.mcdermott{at}leeds.ac.uk)
                            1. Leeds Institute of Molecular Medicine, United Kingdom

                              Abstract

                              Objective: To characterise and investigate the functional consequences of a novel TNFRSF1A splice site mutation causing TRAPS in a 16 year old male patient and his mother.

                              Methods: Mutational DNA screening was performed in the patient and his mother. Western blotting was used to analyse protein expression levels of TNFR1. A multiplex bead immunoassay was used to quantify serum levels of range of cytokines, and an ELISA-based transcription factor assay to measure NF-κB transactivation. Serum levels of soluble TNFR1 (sTNFR1) were measured by ELISA and FACS analysis used to measure monocyte TNFR1 cell surface expression.

                              Results: A novel mutation, c.472+1G>A (C158delinsYERSSPEAKPSPHPRG), involving a splice site in intron 4 of TNFRSF1A, was found in both the proband and affected mother leading to a 45 nucleotide insertion of intronic DNA into the mRNA, resulting in an in-frame insertion of 15 amino acids in the mature TNFR1 protein and a deletion of a cysteine residue C129(158) in cysteine rich domain (CRD) 3. The patients had reduced serum sTNFR1 and surface expression levels of TNFR1, with marked increases in both pro- and anti- inflammatory cytokine. Their peripheral blood mononuclear cells (PBMC) had increased basal NF-κB activation compared with healthy controls and also had increased p50 nuclear expression following TNF stimulation compared with PBMC from healthy controls, as well as T50M (T79M) and C88R (C117R) TRAPS patients and RA patients.

                              Conclusion: A novel, TRAPS causing, TNFRSF1A splice site mutation is associated with decreased sTNFR1 levels, cell surface and whole cell extract expression, and increased NF-κB transcription factor activation.

                              • NF-&[kappa]B
                              • TRAPS
                              • autoinflammatory
                              • mutation

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