Villey I, de Chasseval R, de Villartay J P
Développement Normal et Pathologique du Système Immunitaire INSERM U429, Hôpital Necker Enfants Malades, Paris, France.
Eur J Immunol. 1999 Dec;29(12):4072-80. doi: 10.1002/(SICI)1521-4141(199912)29:12<4072::AID-IMMU4072>3.0.CO;2-E.
TEA (T early alpha) is a genetic element located upstream of the TCR-Jalpha cluster. Thymocytes from mice carrying a targeted deletion of TEA do not rearrange their TCRalpha locus on a window spanning the first nine Jalpha segments. This led us to the hypothesis of TEA having a "rearrangement focusing" activity on the 5' side of the TCR-Jalpha region. We analyzed DNAseI and "phylogenetic" footprints within the TEA promoter in an attempt to identify trans-acting factors that could account for its regulatory function on DNA accessibility. One of these footprints corresponded to a putative DNA-binding site for an orphan nuclear receptor of the ROR / RZR family. The RORgammaT cDNA clone was isolated from a thymus library using a probe corresponding to the DNA-binding domain of RORgamma / TOR. RORgammaT is a thymus-specific isoform of RORgamma, expressed almost exclusively in immature double-positive thymocytes. RORgammaT binds, to the TEA promoter in vitro. Lastly, the expression of RORgammaT is stimulated in two situations that mimic activation through the pre-TCR and in which the thymocytes have their TCR-alpha locus in an "open", yet unrearranged DNA configuration. We propose that the expression of RORgammaT may be part of the pre-TCR activation cascade leading to the maturation of alpha / beta T cells and may participate in the regulation of DNA accessibility in the TCR-Jalpha locus.
TEA(T早期α)是位于TCR-Jα基因簇上游的一种遗传元件。携带TEA靶向缺失的小鼠的胸腺细胞在跨越前九个Jα片段的窗口上不会重排其TCRα基因座。这使我们提出了TEA在TCR-Jα区域5'侧具有“重排聚焦”活性的假说。我们分析了TEA启动子内的DNA酶I和“系统发育”足迹,试图鉴定可能解释其对DNA可及性调节功能的反式作用因子。其中一个足迹对应于ROR/RZR家族孤儿核受体的一个假定DNA结合位点。使用与RORγ/TOR的DNA结合域相对应的探针从胸腺文库中分离出RORγT cDNA克隆。RORγT是RORγ的胸腺特异性异构体,几乎只在未成熟的双阳性胸腺细胞中表达。RORγT在体外与TEA启动子结合。最后,在两种模拟通过前TCR激活的情况下,RORγT的表达受到刺激,此时胸腺细胞的TCR-α基因座处于“开放”但未重排的DNA构型。我们提出,RORγT的表达可能是导致α/βT细胞成熟的前TCR激活级联反应的一部分,并可能参与TCR-Jα基因座中DNA可及性的调节。