79
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Genetic Analysis of MEFV Gene Pyrin Domain in Patients With Behçet's Disease

      other

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Objectives. Behçet's disease (BD) is a systemic vasculitis with recurrent oral and genital ulcers and uveitis. MEFV gene, which is the main factor in familial Mediterranean fever (FMF), is also reported to be a susceptibility gene for BD. The pyrin domain of MEFV gene is a member of death-domain superfamily and has been proposed to regulate inflammatory signaling in myeloid cells. This study was designed to determine if mutations in pyrin domain of MEFV gene are involved in BD. Methods. We analyzed the pyrin domain of MEFV gene in 54 Turkish patients with BD by PCR-analysis and direct sequencing. Results. Neither deletion or insertion mutations nor point mutations in pyrin domain were found in any patient. Conclusion. Although pyrin gene mutations have been reported in patients with BD, pyrin domain is not mutated. However, alterations in other regions of MEFV gene and interaction between pyrin domains are needed to be further investigated.

          Related collections

          Most cited references34

          • Record: found
          • Abstract: not found
          • Article: not found

          Behçet's disease.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Inflammatory caspases: linking an intracellular innate immune system to autoinflammatory diseases.

            Caspases not only play an essential role during apoptotic cell death, but a subfamily of them-the inflammatory caspases-are associated with immune responses to microbial pathogens. Activation of inflammatory caspases, such as caspase-1 and caspase-5, occurs upon assembly of an intracellular complex, designated the inflammasome. This results in the cleavage and activation of the proinflammatory cytokines IL-1beta and IL-18. Mutations in one of the scaffold proteins of the inflammasome, NALP3/Cryopyrin, are associated with autoinflammatory disorders underscoring the importance of regulating inflammatory caspase activation.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever. The International FMF Consortium.

              Familial Mediterranean fever (FMF) is a recessively inherited disorder characterized by dramatic episodes of fever and serosal inflammation. This report describes the cloning of the gene likely to cause FMF from a 115-kb candidate interval on chromosome 16p. Three different missense mutations were identified in affected individuals, but not in normals. Haplotype and mutational analyses disclosed ancestral relationships among carrier chromosomes in populations that have been separated for centuries. The novel gene encodes a 3.7-kb transcript that is almost exclusively expressed in granulocytes. The predicted protein, pyrin, is a member of a family of nuclear factors homologous to the Ro52 autoantigen. The cloning of the FMF gene promises to shed light on the regulation of acute inflammatory responses.
                Bookmark

                Author and article information

                Journal
                Mediators Inflamm
                MI
                Mediators of Inflammation
                Hindawi Publishing Corporation
                0962-9351
                2006
                20 March 2006
                : 2006
                : 3
                : 41783
                Affiliations
                1Department of Medical Genetics, Faculty of Medicine, Zonguldak Karaelmas University, 67600 Zonguldak, Turkey
                2Department of Medical Genetics, Meram Medical Faculty, Selcuk University, 42080 Konya, Turkey
                3Department of Molecular Biology and Genetics, Bilkent University, 06800 Ankara, Turkey
                4Department of Dermatology, Baskent University, 42080 Konya, Turkey
                Author notes
                Article
                10.1155/MI/2006/41783
                1592598
                16951489
                0b648a56-11dd-4322-82f9-1a74a14dfade
                Copyright © 2006 Ahmet Dursun et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 3 January 2006
                : 20 January 2006
                : 20 January 2006
                Categories
                Research Communication

                Immunology
                Immunology

                Comments

                Comment on this article