Kerwitz Yvonne, Kühn Uwe, Lilie Hauke, Knoth Anne, Scheuermann Till, Friedrich Henning, Schwarz Elisabeth, Wahle Elmar
Institut für Biochemie and Institut für Biotechnologie, Martin-Luther-Universität Halle, Kurt-Mothes-Strasse 3, D-06120 Halle, Germany.
EMBO J. 2003 Jul 15;22(14):3705-14. doi: 10.1093/emboj/cdg347.
During polyadenylation of mRNA precursors in metazoan cells, poly(A) polymerase is stimulated by the nuclear poly(A) binding protein PABPN1. We report that stimulation depends on binding of PABPN1 to the substrate RNA directly adjacent to poly(A) polymerase and results in an approximately 80-fold increase in the apparent affinity of poly(A) polymerase for RNA without significant effect on catalytic efficiency. PABPN1 associates directly with poly(A) polymerase either upon allosteric activation by oligo(A) or, in the absence of RNA, upon deletion of its N-terminal domain. The N-terminal domain of PABPN1 may function to inhibit undesirable interactions of the protein; the inhibition is relieved upon RNA binding. Tethering of poly(A) polymerase is mediated largely by the C-terminal domain of PABPN1 and is necessary but not sufficient for stimulation of the enzyme; an additional interaction dependent on a coiled-coil structure located within the N-terminal domain of PABPN1 is required for a productive interaction.
在后生动物细胞中,mRNA前体的聚腺苷酸化过程中,聚(A)聚合酶受到核聚(A)结合蛋白PABPN1的刺激。我们报告称,这种刺激取决于PABPN1与紧邻聚(A)聚合酶的底物RNA的结合,并且导致聚(A)聚合酶对RNA的表观亲和力增加约80倍,而对催化效率没有显著影响。PABPN1在被寡聚(A)变构激活后,或者在没有RNA的情况下,通过缺失其N端结构域,直接与聚(A)聚合酶结合。PABPN1的N端结构域可能起到抑制该蛋白不良相互作用的作用;RNA结合后这种抑制作用会解除。聚(A)聚合酶的拴系主要由PABPN1的C端结构域介导,这对酶的刺激是必要的,但并不充分;PABPN1的N端结构域内的一个依赖于卷曲螺旋结构的额外相互作用对于有效的相互作用是必需的。