Department of Biochemistry, University of Wisconsin-Madison, Madison, United States.
Biophysics Graduate Program, University of Wisconsin-Madison, Madison, United States.
Elife. 2017 Aug 22;6:e27592. doi: 10.7554/eLife.27592.
The spliceosome must identify the correct splice sites (SS) and branchsite (BS) used during splicing. E complex is the earliest spliceosome precursor in which the 5' SS and BS are defined. Definition occurs by U1 small nuclear ribonucleoprotein (snRNP) binding the 5' SS and recognition of the BS by the E complex protein (ECP) branchpoint bridging protein (BBP). We have used single molecule fluorescence to study U1 and BBP interactions with RNAs. E complex is dynamic and permits frequent redefinition of the 5' SS and BS. BBP influences U1 binding at the 5' SS by promoting long-lived complex formation. ECPs facilitate U1 association with RNAs with weak 5' SS and prevent U1 accumulation on RNAs containing hyperstabilized 5' SS. The data reveal a mechanism for how U1 binds the 5' SS and suggest that E complex harnesses this mechanism to stimulate recruitment and retention of U1 on introns.
剪接体必须识别剪接过程中使用的正确剪接位点(SS)和分支位点(BS)。E 复合物是最早的剪接体前体,其中 5' SS 和 BS 被定义。通过 U1 小核核糖核蛋白(snRNP)结合 5' SS 和 E 复合物蛋白(ECP)分支点桥接蛋白(BBP)识别 BS 来实现定义。我们已经使用单分子荧光技术研究了 U1 和 BBP 与 RNA 的相互作用。E 复合物是动态的,允许频繁重新定义 5' SS 和 BS。BBP 通过促进长寿命复合物的形成来影响 U1 在 5' SS 上的结合。ECPs 促进与 5' SS 较弱的 RNA 结合 U1,并防止 U1 在含有超稳定 5' SS 的 RNA 上积累。这些数据揭示了 U1 结合 5' SS 的机制,并表明 E 复合物利用该机制来刺激 U1 在内含子上的募集和保留。