Marecki Sylvia, McCarthy Kevin M, Nikolajczyk Barbara S
Department of Medicine, Boston University School of Medicine, 650 Albany Street X-438, Boston, MA 02118, USA.
Mol Immunol. 2004 Jan;40(10):723-31. doi: 10.1016/j.molimm.2003.08.007.
The hematopoietic-specific transcription factor PU.1 is a chromatin accessibility factor, based on analysis of the immunoglobulin heavy chain intronic (mu) enhancer. Whether PU.1 functions as an accessibility factor for additional PU.1-regulated genes is unknown. Outside the constraints of chromatin, PU.1 binds and activates transcription through both mu and kappa3' immunoglobulin enhancers, among others. The DNA-binding ETS domain of PU.1 is sufficient for activating both enhancers in an extrachromosomal context. New data show that the ETS domain of PU.1 is sufficient for increasing accessibility of a closed mu enhancer chromatin structure proximal to the PU.1-binding site. In contrast, PU.1 does not alter widespread chromatin accessibility. Furthermore, PU.1 does not induce accessibility proximal or distal to its binding site on the kappa3' enhancer. Taken together the data demonstrate that PU.1 induces chromatin accessibility proximal to its binding site at a locus activated early in development, the mu locus. PU.1 does not function as an accessibility factor for the kappa3' enhancer, which regulates a locus important for later stages of B cell development. We conclude that PU.1 is a context-dependent chromatin accessibility factor that, alone, cannot establish widespread accessibility required for critical developmental processes such as antigen receptor recombination.
基于对免疫球蛋白重链内含子(μ)增强子的分析,造血特异性转录因子PU.1是一种染色质可及性因子。PU.1是否作为其他受PU.1调控基因的可及性因子尚不清楚。在染色质的限制之外,PU.1通过μ和κ3'免疫球蛋白增强子等结合并激活转录。PU.1的DNA结合ETS结构域足以在染色体外环境中激活这两种增强子。新数据表明,PU.1的ETS结构域足以增加靠近PU.1结合位点的封闭μ增强子染色质结构的可及性。相比之下,PU.1不会改变广泛的染色质可及性。此外,PU.1不会在κ3'增强子上其结合位点的近端或远端诱导可及性。综合这些数据表明,PU.1在发育早期激活的一个位点——μ位点,诱导其结合位点近端的染色质可及性。PU.1不作为κ3'增强子的可及性因子,κ3'增强子调节对B细胞发育后期很重要的一个位点。我们得出结论,PU.1是一种依赖于上下文的染色质可及性因子,单独它不能建立关键发育过程(如抗原受体重组)所需的广泛可及性。