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The MHC-Specific Enhanceosome and Its Role in MHC Class I and β2-Microglobulin Gene Transactivation

机译:MHC特异性增强体及其在MHC I类和β2-微球蛋白基因反式激活中的作用

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The promoter regions of MHC class I and β2-microglobulin (β2m) genes posses a regulatory module consisting of S, X, and Y boxes, which is shared by MHC class II and its accessory genes. In this study we show that, similar to MHC class II, the SXY module in MHC class I and β2m promoters is cooperatively bound by a multiprotein complex containing regulatory factor X, CREB/activating transcription factor, and nuclear factor Y. Together with the coactivator class II transactivator this multiprotein complex drives transactivation of these genes. In contrast to MHC class II, the multiprotein complex has an additional function in the constitutive transactivation of MHC class I and β2m genes. The requirement for all transcription factors in the complex and correct spacing of the binding sites within the SXY regulatory module for complex formation and functioning of this multiprotein complex strongly suggests that this complex can be regarded as a bona fide enhanceosome. The general coactivators CREB binding protein, p300, general control nonderepressible-5, and p300/CREB binding protein-associated factor exert an ancillary function in MHC class I and β2m transactivation, but exclusively through the class II transactivator component of this enhanceosome. Thus, the SXY module is the basis for a specific enhanceosome important for the constitutive and inducible transactivation of MHC class I and β2m genes.
机译:MHC I类和β2-微球蛋白(β2m)基因的启动子区域具有由S,X和Y框组成的调控模块,该模块由MHC II类及其辅助基因共享。在这项研究中,我们表明,类似于MHC II类,MHC I类和β2m启动子中的SXY模块被包含调节因子X,CREB ​​/活化转录因子和核因子Y的多蛋白复合物协同结合。 II类反式激活因子,这种多蛋白复合物驱动这些基因的反式激活。与II类MHC相反,多蛋白复合物在MHC I类和β2m基因的组成型反式激活中具有其他功能。 SXY调节模块内结合位点的复杂且正确间距中所有转录因子对于该多蛋白复合物的形成和功能的需求强烈表明,该复合物可被视为真正的增强体。一般的共激活因子CREB结合蛋白,p300,一般控制不可抑制5和p300 / CREB结合蛋白相关因子在MHC I类和β2m反式激活中发挥辅助功能,但仅通过该增强体的II类反式激活剂成分。因此,SXY模块是特定增强体的基础,该增强体对MHC I类和β2m基因的组成型和诱导型反式激活很重要。

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