Brosi R, Gröning K, Behrens S E, Lührmann R, Krämer A
Département de Biologie Cellulaire, Sciences III, Université de Genève, Switzerland.
Science. 1993 Oct 1;262(5130):102-5. doi: 10.1126/science.8211112.
In the assembly of a prespliceosome, U2 small nuclear ribonucleoprotein (snRNP) functions in pre-messenger RNA (mRNA) splicing together with splicing factors (SFs) 3a, SF3b, and several other proteins. The 17S but not the 12S form of U2 snRNP is active in splicing-complex formation. Here it is shown that the SF3a subunits correspond to three of the 17S U2 snRNP-specific polypeptides. SF3a interacts with U2 snRNP in the presence of SF3b to generate a structure similar to 17S U2 snRNP, which suggests a function for SF3a and SF3b in the incorporation of U2 snRNP into the spliceosome. Furthermore, the 60-kilodalton subunit of SF3a is related to the yeast splicing protein PRP9.
在剪接体前体的组装过程中,U2小核核糖核蛋白(snRNP)与剪接因子(SFs)3a、SF3b以及其他几种蛋白质一起参与前体信使RNA(mRNA)的剪接。U2 snRNP的17S形式而非12S形式在剪接复合体形成中具有活性。本文表明,SF3a亚基对应于17S U2 snRNP特异性多肽中的三种。在SF3b存在的情况下,SF3a与U2 snRNP相互作用,生成类似于17S U2 snRNP的结构,这表明SF3a和SF3b在将U2 snRNP整合到剪接体中具有作用。此外,SF3a的60千道尔顿亚基与酵母剪接蛋白PRP9相关。