Matesanz Fuencisla, Fedetz Maria, Leyva Laura, Delgado Concepción, Fernández Oscar, Alcina Antonio
Instituto de Parasitología y Biomedicina López Neyra, CSIC, C/Ventanilla 11, 18001 Granada, Spain.
J Neuroimmunol. 2004 Mar;148(1-2):212-7. doi: 10.1016/j.jneuroim.2003.12.001.
The -330 IL2 gene promoter polymorphism has been associated with multiple sclerosis (MS) [J. Neuroimmunol. 119 (2001) 101], but the basis underlying this association remains unknown to date. In the present work, we have found that IL2 promoter-luciferase constructs, transfected in Jurkat cell line, showed twofold higher levels of gene expression in the -330 G allele. However, the transcriptional effect of this polymorphism in lymphocytes showed that the G allele was related to lower expression of IL2. This difference increased in the patient group. Divergence between in vivo and in vitro influence of the -330 IL2 promoter polymorphic site suggests the existence of additional unknown polymorphisms affecting gene regulation. Our data show an increased IL2 expression among GT and TT genotypes previously associated with susceptibility to MS.
IL2基因启动子 -330位点的多态性已被证实与多发性硬化症(MS)相关[《神经免疫学杂志》119 (2001) 101],但迄今为止,这种关联背后的基础仍不清楚。在本研究中,我们发现,转染到Jurkat细胞系中的IL2启动子 - 荧光素酶构建体显示,-330 G等位基因中的基因表达水平高出两倍。然而,这种多态性在淋巴细胞中的转录效应表明,G等位基因与IL2的低表达有关。在患者组中,这种差异更加明显。-330 IL2启动子多态性位点在体内和体外影响之间的差异表明,存在其他影响基因调控的未知多态性。我们的数据显示,先前与MS易感性相关的GT和TT基因型中IL2表达增加。