Woo Caroline J, Martin Alberto, Scharff Matthew D
Department of Cell Biology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Chanin 403, Bronx, NY 10461, USA.
Immunity. 2003 Oct;19(4):479-89. doi: 10.1016/s1074-7613(03)00261-9.
Somatic hypermutation (SHM) requires selective targeting of the mutational machinery to the variable region of the immunoglobulin heavy chain gene. The induction of SHM in the BL2 cell line upon costimulation is associated with hyperacetylation of the chromatin at the variable region but not at the constant region. The V region-restricted histone hyperacetylation resulting from costimulation occurs independent of AID expression and mutation. Interestingly, costimulation in the presence of Trichostatin A causes hyperacetylation of histones associated with the constant region and extends mutations to the constant region. Under this condition, promoter proximal mutations are observed in the variable region as well. The overexpression of AID results in a similar deregulation of mutational targeting. Our results indicate that the stimulation of SHM in BL2 cells activates two independent pathways resulting in histone modifications that permit induced levels of AID to selectively target the variable region for mutation.
体细胞高频突变(SHM)需要将突变机制选择性地靶向免疫球蛋白重链基因的可变区。共刺激时BL2细胞系中SHM的诱导与可变区而非恒定区染色质的高乙酰化相关。共刺激导致的V区限制性组蛋白高乙酰化独立于AID表达和突变而发生。有趣的是,在曲古抑菌素A存在下的共刺激会导致与恒定区相关的组蛋白高乙酰化,并使突变延伸至恒定区。在这种情况下,可变区也会观察到启动子近端突变。AID的过表达导致类似的突变靶向失调。我们的结果表明,BL2细胞中SHM的刺激激活了两条独立的途径,导致组蛋白修饰,使诱导水平的AID能够选择性地靶向可变区进行突变。