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大鼠4号染色体上关节炎易感基因座的高分辨率定位及调控表型的特征分析。

High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypes.

作者信息

Ribbhammar Ulrica, Flornes Line, Bäckdahl Liselotte, Luthman Holger, Fossum Sigbjörn, Lorentzen Johnny C

机构信息

Rheumatology Unit, Center for Molecular Medicine, L8:04, Karolinska Hospital, S-171 76 Stockholm, Sweden.

出版信息

Hum Mol Genet. 2003 Sep 1;12(17):2087-96. doi: 10.1093/hmg/ddg224. Epub 2003 Jul 8.

Abstract

The rat Natural Killer cell gene Complex (NKC) encodes molecules that can regulate immunity. It is located within an interval on DA rat chromosome 4 (RNO4) that is linked to immune-mediated inflammatory joint diseases, including oil-induced arthritis (OIA). We aimed to test the hypothesis that NKC regulates arthritis, by performing advanced mapping of arthritis and additional phenotypes induced by an intradermal injection of incomplete Freund's adjuvant-oil. Reciprocal transfer of RNO4 intervals established that alleles from DA confer arthritis susceptibility to inbred LEW.1AV1 and PVG.1AV1 rats, whereas LEW.1AV1 and PVG.1AV1 alleles confer resistance to inbred DA. Subcongenic strains with PVG.1AV1 alleles introduced on DA allowed mapping of disease predisposition to 0.8 cM on the cytogenetic band 4q42, within the quantitative trait locus oil-induced arthritis-2 (Oia2), but outside the NKC. Alleles in Oia2 regulated arthritis in an additive fashion, and determined arthritis incidence, severity and day of onset, in both males and females. Besides macroscopic joint-inflammation, Oia2 also regulated other oil-induced phenotypes, including lymphoplasia and plasma levels of the inflammation marker alpha1-acid glycoprotein. The high-impact Oia2 region harbors gene sequences similar to human C3AR1, Ribosomal protein L7, DNAJA2, C-type lectins, C1s and CD163. These candidate disease genes may be of general interest, given that rat 4q42, and the syntenic mouse 6F2 and human 12p13 regions are linked to several inflammatory diseases, including rheumatoid arthritis.

摘要

大鼠自然杀伤细胞基因复合体(NKC)编码可调节免疫的分子。它位于DA大鼠4号染色体(RNO4)上的一个区间内,该区间与免疫介导的炎性关节疾病相关,包括油诱导性关节炎(OIA)。我们旨在通过对皮内注射不完全弗氏佐剂-油诱导的关节炎及其他表型进行精细定位,来验证NKC调节关节炎的假说。RNO4区间的相互转移表明,DA的等位基因使近交系LEW.1AV1和PVG.1AV1大鼠易患关节炎,而LEW.1AV1和PVG.1AV1的等位基因则使近交系DA具有抗性。在DA背景上引入PVG.1AV1等位基因的亚同源基因系,可将疾病易感性定位到细胞遗传带4q42上0.8 cM处,位于数量性状基因座油诱导性关节炎-2(Oia2)内,但在NKC之外。Oia2中的等位基因以累加方式调节关节炎,并决定了雄性和雌性的关节炎发病率、严重程度和发病时间。除了宏观的关节炎症外,Oia2还调节其他油诱导的表型,包括淋巴细胞增生和炎症标志物α1-酸性糖蛋白的血浆水平。具有高影响力的Oia2区域包含与人类C3AR1、核糖体蛋白L7、DNAJA2、C型凝集素、C1s和CD163相似的基因序列。鉴于大鼠4q42以及同区域的小鼠6F2和人类12p13区域与包括类风湿关节炎在内的几种炎性疾病相关,这些候选疾病基因可能具有普遍意义。

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