IL2RA基因位点两个新调控元件的鉴定

F. Rosa, P. Rameil, M. Algarte-Genin, M. Bedotto, P. Ferrier, P. Cauchy, J. Imbert
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引用次数: 2

摘要

调节性t细胞(Tregs)表达由IL2RA基因编码的白细胞介素2 (IL-2)受体CD25的高亲和力链。在成熟CD4+ T淋巴细胞抗原依赖性激活的背景下,IL2RA是最广泛表征的基因之一,其调控区域及其与细胞表面受体的功能联系及其相关的信号转导级联。然而,越来越多的证据强烈表明,在这个由6个特征明确的调控区域组成的已经很复杂的拼图中,它们是一些缺失的部分。在这里,通过主要结合芯片基因组足迹方法和几项ChIP-seq研究的荟荟性分析,我们确定并表征了2个新的假定的cd28响应元件。我们发现,最近表征的+11 kb的内含子增强子含有一个功能性的CREB位点。此外,我们还发现了一个由两个GAAA重复序列组成的抑制元件,位于IL2RA基因上游4kb处,大部分是先前鉴定的增强子。质谱分析显示聚adp -核糖聚合酶1 (PARP-1)是结合该元件的复合物的一部分。总之,我们的观察扩展了我们对这种复杂组织在T细胞反应方面提供的多种选择的分子基础的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Two Novel Regulatory Elements in the IL2RA Gene Locus
Regulatory T-cells (Tregs) express the high-affinity chain of the interleukin 2 (IL-2) receptor, CD25, encoded by the IL2RA gene. IL2RA is one of the most extensively characterized genes regarding its regulatory regions and their functional links to cell surface receptors and their associated signal transduction cascade in the context of the antigen-dependent activation of mature CD4+ T lymphocyte. However, converging evidences strongly suggested that they were some missing pieces in this already complex puzzle made of 6 well-characterized regulatory regions. Here, by combining principally in silico genomic footprinting approach and meta-analysis of several ChIP-seq studies, we identified and characterized 2 new putative CD28-responsive elements. We show that a recently-characterized intronic enhancer at +11 kb harbors a functional CREB site. Further, we evidence a repressor element consisting of two GAAA repeats located 5’-most of a previously identified enhancer 4 kb upstream of the IL2RA gene. Massspectrometry analyses revealed Poly ADP-ribose polymerase 1 (PARP-1) as part of the complexes binding this element. Altogether, our observations extend our understanding of the molecular basis of the multiple options offered by such a complex organization in term of T cell responses.
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