Schebesta Alexandra, McManus Shane, Salvagiotto Giorgia, Delogu Alessio, Busslinger Georg A, Busslinger Meinrad
Research Institute of Molecular Pathology, Vienna Biocenter, Dr. Bohr-Gasse 7, A-1030 Vienna, Austria.
Immunity. 2007 Jul;27(1):49-63. doi: 10.1016/j.immuni.2007.05.019. Epub 2007 Jul 19.
The transcription factor Pax5 represses B lineage-inappropriate genes and activates B cell-specific genes in B lymphocytes. Here we have identified 170 Pax5-activated genes. Conditional mutagenesis demonstrated that the Pax5-regulated genes require continuous Pax5 activity for normal expression in pro-B and mature B cells. Expression of half of the Pax5-activated genes is either absent or substantially reduced upon Pax5 loss in plasma cells. Direct Pax5 target genes were identified based on their protein synthesis-independent activation by a Pax5-estrogen receptor fusion protein. Chromatin immunoprecipitation (ChIP) of Pax5 together with chromatin profiling by ChIP-on-chip analysis demonstrated that Pax5 directly activates the chromatin at promoters or putative enhancers of Pax5 target genes. The Pax5-activated genes code for key regulatory and structural proteins involved in B cell signaling, adhesion, migration, antigen presentation, and germinal-center B cell formation, thus revealing a complex regulatory network that is activated by Pax5 to control B cell development and function.
转录因子Pax5可抑制B淋巴细胞中不适合B细胞系的基因,并激活B细胞特异性基因。在此,我们鉴定出了170个由Pax5激活的基因。条件性诱变表明,Pax5调控的基因在原B细胞和成熟B细胞中正常表达需要持续的Pax5活性。在浆细胞中,当Pax5缺失时,一半由Pax5激活的基因的表达缺失或显著降低。基于Pax5-雌激素受体融合蛋白对其不依赖蛋白质合成的激活作用,鉴定出了直接的Pax5靶基因。Pax5的染色质免疫沉淀(ChIP)以及芯片上的ChIP分析进行的染色质分析表明,Pax5直接激活Pax5靶基因启动子或假定增强子处的染色质。Pax5激活的基因编码参与B细胞信号传导、黏附、迁移、抗原呈递和生发中心B细胞形成的关键调节蛋白和结构蛋白,从而揭示了一个由Pax5激活以控制B细胞发育和功能的复杂调控网络。