Hernández-Munain Cristina, Krangel Michael S
Basel Institute for Immunology, Basel, Switzerland.
J Immunol. 2002 Oct 15;169(8):4362-9. doi: 10.4049/jimmunol.169.8.4362.
Enhancers and promoters within TCR loci functionally collaborate to modify chromatin structure and to confer accessibility to the transcription and V(D)J recombination machineries during T cell development in the thymus. Two enhancers at the TCRalphadelta locus, the TCR alpha enhancer and the TCR delta enhancer (Edelta), are responsible for orchestrating the distinct developmental programs for V(D)J recombination and transcription of the TCR alpha and delta genes, respectively. Edelta function depends critically on transcription factors core binding factor (CBF)/polyoma enhancer-binding protein 2 (PEBP2) and c-Myb as measured by transcriptional activation of transiently transfected substrates in Jurkat cells, and by activation of V(D)J recombination within chromatin-integrated substrates in transgenic mice. To understand the molecular mechanisms for synergy between these transcription factors in the context of chromatin, we used in vivo footprinting to study the requirements for protein binding to Edelta within wild-type and mutant versions of a human TCR delta minilocus in stably transfected Jurkat cells. Our data indicate that CBF/PEBP2 plays primarily a structural role as it induces a conformational change in the enhanceosome that is associated with augmented binding of c-Myb. In contrast, c-Myb has no apparent affect on CBF/PEBP2 binding, but is critical for transcriptional activation. Thus, our data reveal distinct functions for c-Myb and CBF/PEBP2 in the assembly and function of an Edelta enhanceosome in the context of chromatin in vivo.
在胸腺中T细胞发育过程中,TCR基因座内的增强子和启动子在功能上相互协作,以改变染色质结构,并使转录和V(D)J重组机制能够接近。TCRαδ基因座上的两个增强子,即TCRα增强子和TCRδ增强子(Edelta),分别负责协调TCRα和δ基因V(D)J重组和转录的不同发育程序。通过Jurkat细胞中瞬时转染底物的转录激活以及转基因小鼠中染色质整合底物内V(D)J重组的激活来衡量,Edelta功能关键依赖于转录因子核心结合因子(CBF)/多瘤病毒增强子结合蛋白2(PEBP2)和c-Myb。为了在染色质背景下理解这些转录因子之间协同作用的分子机制,我们使用体内足迹法研究了稳定转染的Jurkat细胞中野生型和突变型人TCRδ微基因座内蛋白质与Edelta结合的要求。我们的数据表明,CBF/PEBP2主要起结构作用,因为它诱导增强体发生构象变化,这与c-Myb结合增加有关。相比之下,c-Myb对CBF/PEBP2结合没有明显影响,但对转录激活至关重要。因此,我们的数据揭示了在体内染色质背景下,c-Myb和CBF/PEBP2在Edelta增强体的组装和功能中具有不同的功能。