T-cell receptor V alpha and C alpha alleles associated with multiple and myasthenia gravis.
Author(s) -
Jorge R. Oksenberg,
Martina A. Sherritt,
A. B. Begovich,
H.A. Erlich,
Claude C.A. Bernard,
Luigi Luca Cavalli-Sforza,
Lawrence Steinman
Publication year - 1989
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.86.3.988
Subject(s) - myasthenia gravis , restriction fragment length polymorphism , microbiology and biotechnology , southern blot , biology , polymerase chain reaction , complementary dna , alpha chain , allele , alpha (finance) , t cell receptor , population , allele frequency , restriction fragment , genetics , gene , t cell , immunology , medicine , construct validity , nursing , immune system , environmental health , patient satisfaction
Polymorphic markers in genes encoding that alpha chain of the human T-cell receptor (TcR) have been detected by Southern blot analysis in Pss I digests. Polymorphic bands were observed at 6.3 and 2.0 kilobases (kb) with frequencies of 0.30 and 0.44, respectively, in the general population. Using the polymerase chain reaction (PCR) method, we amplified selected sequences derived from the full-length TcR alpha cDNA probe. These PCR products were used as specific probes to demonstrate that the 6.3-kb polymorphic fragment hybridizes to the variable (V)-region probe and the 2.0-kb fragment hybridizes to the constant (C)-region probe. Segregation of the polymorphic bands was analyzed in family studies. To look for associations between these markers and autoimmune diseases, we have studied the restriction fragment length polymorphism distribution of the Pss I markers in patients with multiple sclerosis, myasthenia gravis, and Graves disease. Significant differences in the frequency of the polymorphic V alpha and C alpha markers were identified between patients and healthy individuals.
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