Wallin J J, Gackstetter E R, Koshland M E
Immunology Division, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, CA 94720, USA.
Science. 1998 Mar 20;279(5358):1961-4. doi: 10.1126/science.279.5358.1961.
During a B cell immune response, the transcription factor BSAP maintains its activator functions but is relieved of its repressor functions. This selective targeting of BSAP activities was shown to be regulated by a concentration-dependent mechanism whereby activator motifs for BSAP had a 20-fold higher binding affinity than repressor motifs. An exchange of activator and repressor motifs, however, showed that the context of the motif, rather than the affinity, determined whether BSAP operated as an activator or repressor.
在B细胞免疫反应过程中,转录因子BSAP维持其激活功能,但解除了其抑制功能。已证明BSAP活性的这种选择性靶向是由浓度依赖性机制调节的,据此BSAP的激活基序比抑制基序具有高20倍的结合亲和力。然而,激活基序与抑制基序的交换表明,基序的背景而非亲和力决定了BSAP是作为激活剂还是抑制剂发挥作用。