Delves P J, Lund T, Axford J S, Alavi-Sadrieh A, Lydyard P M, MacKenzie L, Smith M D, Kidd V J
Department of Immunology, University College and Middlesex School of Medicine, London, UK.
Arthritis Rheum. 1990 Nov;33(11):1655-64. doi: 10.1002/art.1780331108.
We used restriction endonuclease digestion of leukocyte DNA to assess the structural integrity of an N-acetylglucosamine beta 1----4 galactosyltransferase (GalTase)-associated (GTA) protein kinase gene in rheumatoid arthritis (RA) patients. This analysis provides evidence that the gross structure of the GTA protein kinase gene locus remains intact in patients with defective galactosylation and that this gene locus is polymorphic both in normal individuals and in patients with RA, although no polymorphisms unique to RA patients were observed. Initial data on the expression of this gene indicate that comparable levels of GTA protein kinase messenger RNA are present in the lymphocytes of normal individuals and RA patients, irrespective of whether lymphocytes were obtained from patients with decreased or normal levels of galactosylation.
我们采用白细胞DNA的限制性内切酶消化法,来评估类风湿性关节炎(RA)患者中与N-乙酰葡糖胺β1----4半乳糖基转移酶(GalTase)相关的(GTA)蛋白激酶基因的结构完整性。该分析提供了证据,表明在半乳糖基化存在缺陷的患者中,GTA蛋白激酶基因位点的总体结构保持完整,并且该基因位点在正常个体和RA患者中均具有多态性,尽管未观察到RA患者特有的多态性。关于该基因表达的初步数据表明,正常个体和RA患者的淋巴细胞中存在相当水平的GTA蛋白激酶信使RNA,无论淋巴细胞是从半乳糖基化水平降低或正常的患者中获取的。