首页> 外文期刊>Experimental and Clinical Immunogenetics >Nucleotide sequences specific for nonnominal immunoglobulin allotypes in rheumatoid arthritis patients and in normal individuals and their expression in synovial tissue of rheumatoid arthritis patients.
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Nucleotide sequences specific for nonnominal immunoglobulin allotypes in rheumatoid arthritis patients and in normal individuals and their expression in synovial tissue of rheumatoid arthritis patients.

机译:类风湿性关节炎患者和正常个体中非标称免疫球蛋白同种异型的特定核苷酸序列及其在类风湿性关节炎患者滑膜组织中的表达。

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摘要

The production of antibodies against nonnominal immunoglobulin allotypes in rheumatoid arthritis (RA) patients suggests that the immune system of these patients has been exposed to such foreign allotypes. The presence of nonnominal allotypes is, however, a genetic enigma. We searched for nucleotide sequences specific for nonnominal G3mg and G3mb copies in individuals homozygous for these alleles. Using a sensitive and specific nested polymerase chain reaction (PCR) method with genomic DNA from blood of 18 RA patients and 5 normal controls, we found G3mg sequences in 18 of 18 tested G3mb homozygous persons. The allele specificity of the PCR fragments was confirmed by sequencing and RFLP analysis. The PCR products contained genomic nonspliced parts of the nonnominal sequences. An analysis of cDNA from inflammatory tissue of 5 RA patients detected nonnominal G3mb sequences in 1 of 3 tested G3mg homozygotes and G3mg sequences in 2 of 2 tested G3mb homozygotes. The cDNA-derived PCR products contained sequences from normally spliced nonnominal Ig fragments. The results also showed that the nonnominal Ig sequences were present in very low copy numbers, lower than the Mendelian 1-2 copies per cell. The origin of such a low copy number of Ig gene fragments may be explained by a virus-mediated capture and transfer mechanism of Ig gene fragments generated by the normal Ig switch-associated gene excision process.
机译:类风湿性关节炎(RA)患者中针对非标称免疫球蛋白同种异型的抗体的产生表明这些患者的免疫系统已暴露于此类外源同种异型。然而,非同名异型的存在是遗传的谜。我们在这些等位基因纯合的个体中搜索了特定于标称G3mg和G3mb拷贝的核苷酸序列。使用灵敏且特异性的巢式聚合酶链反应(PCR)方法,对18位RA患者和5位正常对照的血液中的基因组DNA进行检测,我们在18位测试的G3mb纯合子中的18位中发现了G3mg序列。 PCR片段的等位基因特异性通过测序和RFLP分析确认。 PCR产物包含非标称序列的基因组非剪接部分。对来自5名RA患者的炎症组织的cDNA进行分析,发现3个测试的G3mg纯合子中有1个的标称G3mb序列和2个测试的G3mb纯合体中的2个的G3mg序列。 cDNA衍生的PCR产物包含正常剪接的非标称Ig片段的序列。结果还表明,非标称Ig序列的拷贝数非常低,低于每个细胞的孟德尔1-2拷贝。如此低拷贝数的Ig基因片段的起源可以通过病毒介导的正常Ig开关相关基因切除过程产生的Ig基因片段的捕获和转移机制来解释。

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