Leng Lin, Siu Edwin, Bucala Richard
Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut, USA.
Methods Mol Biol. 2020;2080:67-84. doi: 10.1007/978-1-4939-9936-1_7.
Macrophage migration inhibitory factor (MIF) is an upstream proinflammatory cytokine encoded by a functionally polymorphic locus. The promoter region of the human MIF gene contains two polymorphisms. A variable nucleotide tandem repeat at position -794 comprises five to eight CATT repeats (referred to henceforth by numbers from 5 to 8, rs5844572). Gene reporter assays show a proportional increase in transcription with CATT repeat number; the 5-repeat allele leads to low expression, and the 6-, 7-, and 8-repeat alleles lead to correspondingly higher expression of MIF. A second MIF promoter polymorphism comprises a G-to-C single nucleotide polymorphism (SNP) at position -173 (rs755622), which is in strong linkage disequilibrium with -794 7-CATT and is associated with arthritis clinical severity and higher serum and synovial fluid MIF levels. This allele also has been reported to confer improved survival in patients with outpatient pneumonia. In this chapter, we will introduce the methods of genotyping CATT repeats and the MIF -173 G/C from human samples.
巨噬细胞移动抑制因子(MIF)是一种由功能多态性位点编码的上游促炎细胞因子。人类MIF基因的启动子区域包含两种多态性。-794位点的可变核苷酸串联重复序列由5至8个CATT重复序列组成(此后用5至8的数字表示,rs5844572)。基因报告分析表明,转录随CATT重复序列数量成比例增加;5重复等位基因导致低表达,而6、7和8重复等位基因导致MIF相应更高的表达。第二个MIF启动子多态性是-173位点的G到C单核苷酸多态性(SNP,rs755622),它与-794 7-CATT处于强连锁不平衡状态,并且与关节炎临床严重程度以及更高的血清和滑液MIF水平相关。据报道,该等位基因还能提高门诊肺炎患者的生存率。在本章中,我们将介绍对人类样本中CATT重复序列和MIF -173 G/C进行基因分型的方法。