Krawczyk Michal, Peyraud Nicolas, Rybtsova Natalia, Masternak Krzysztof, Bucher Philipp, Barras Emmanuèle, Reith Walter
University of Geneva Medical School, Centre Médical Universitaire, 1 rue Michel-Servet, CH-1211 Geneva, Switzerland.
J Immunol. 2004 Nov 15;173(10):6200-10. doi: 10.4049/jimmunol.173.10.6200.
MHC class II (MHC-II) genes are regulated by an enhanceosome complex containing two gene-specific transcription factors, regulatory factor X complex (RFX) and CIITA. These factors assemble on a strictly conserved regulatory module (S-X-X2-Y) found immediately upstream of the promoters of all classical and nonclassical MHC-II genes as well as the invariant chain (Ii) gene. To identify new targets of RFX and CIITA, we developed a computational approach based on the unique and highly constrained architecture of the composite S-Y motif. We identified six novel S'-Y' modules situated far away from the promoters of known human RFX- and CIITA-controlled genes. Four are situated at strategic positions within the MHC-II locus, and two are found within the Ii gene. These S'-Y' modules function as transcriptional enhancers, are bona fide targets of RFX and CIITA in B cells and IFN-gamma-induced cells, and induce broad domains of histone hyperacetylation. These results reveal a hitherto unexpected level of complexity involving long distance control of MHC-II expression by multiple distal regulatory elements.
主要组织相容性复合体II类(MHC-II)基因由一个增强体复合物调控,该复合物包含两个基因特异性转录因子,即调控因子X复合物(RFX)和II类反式激活因子(CIITA)。这些因子聚集在一个严格保守的调控模块(S-X-X2-Y)上,该模块位于所有经典和非经典MHC-II基因以及恒定链(Ii)基因启动子的紧邻上游。为了鉴定RFX和CIITA的新靶点,我们基于复合S-Y基序独特且高度受限的结构开发了一种计算方法。我们鉴定出六个新的S'-Y'模块,它们位于远离已知人类RFX和CIITA调控基因启动子的位置。其中四个位于MHC-II基因座内的关键位置,两个位于Ii基因内。这些S'-Y'模块作为转录增强子发挥作用,是B细胞和干扰素-γ诱导细胞中RFX和CIITA的真正靶点,并诱导广泛的组蛋白高度乙酰化区域。这些结果揭示了一个迄今未被预料到的复杂程度,即多个远端调控元件对MHC-II表达进行长距离控制。