Das R, Zhou Z, Reed R
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Mol Cell. 2000 May;5(5):779-87. doi: 10.1016/s1097-2765(00)80318-4.
In the current model for spliceosome assembly, U1 snRNP binds to the 5' splice site in the E complex followed by ATP-dependent binding of U2 snRNP to the branchpoint sequence (BPS) in the A complex. Here we report the characterization of highly purified, functional E complex. We provide evidence that this complex contains functional U2 snRNP and that this snRNP is required for E complex assembly. The BPS is not required for U2 snRNP binding in the E complex. These data suggest a model for spliceosome assembly in which U1 and U2 snRNPs first associate with the spliceosome in the E complex and then an ATP-dependent step results in highly stable U2 snRNP binding to the BPS in the A complex.
在当前的剪接体组装模型中,U1 snRNP在E复合物中与5'剪接位点结合,随后U2 snRNP通过ATP依赖的方式与A复合物中的分支点序列(BPS)结合。在此,我们报告了高度纯化的功能性E复合物的特性。我们提供的证据表明,该复合物包含功能性U2 snRNP,并且该snRNP是E复合物组装所必需的。BPS并非E复合物中U2 snRNP结合所必需的。这些数据提示了一种剪接体组装模型,其中U1和U2 snRNPs首先在E复合物中与剪接体结合,然后一个ATP依赖步骤导致U2 snRNP在A复合物中与BPS高度稳定地结合。