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裂殖酵母 Cdc5 N 端结构与功能的研究进展

Structural and functional insights into the N-terminus of Schizosaccharomyces pombe Cdc5.

机构信息

Department of Cell and Developmental Biology, Vanderbilt University Medical Center , Nashville, Tennessee 37232, United States.

出版信息

Biochemistry. 2014 Oct 21;53(41):6439-51. doi: 10.1021/bi5008639. Epub 2014 Oct 8.

Abstract

The spliceosome is a dynamic macromolecular machine composed of five small nuclear ribonucleoparticles (snRNPs), the NineTeen Complex (NTC), and other proteins that catalyze the removal of introns mature to form the mature message. The NTC, named after its founding member Saccharomyces cerevisiae Prp19, is a conserved spliceosome subcomplex composed of at least nine proteins. During spliceosome assembly, the transition to an active spliceosome correlates with stable binding of the NTC, although the mechanism of NTC function is not understood. Schizosaccharomyces pombe Cdc5, a core subunit of the NTC, is an essential protein required for pre-mRNA splicing. The highly conserved Cdc5 N-terminus contains two canonical Myb (myeloblastosis) repeats (R1 and R2) and a third domain (D3) that was previously classified as a Myb-like repeat. Although the N-terminus of Cdc5 is required for its function, how R1, R2, and D3 each contribute to functionality is unclear. Using a combination of yeast genetics, structural approaches, and RNA binding assays, we show that R1, R2, and D3 are all required for the function of Cdc5 in cells. We also show that the N-terminus of Cdc5 binds RNA in vitro. Structural and functional analyses of Cdc5-D3 show that, while this domain does not adopt a Myb fold, Cdc5-D3 preferentially binds double-stranded RNA. Our data suggest that the Cdc5 N-terminus interacts with RNA structures proposed to be near the catalytic core of the spliceosome.

摘要

剪接体是一种由五个小核核糖核蛋白(snRNP)、十九复合物(NTC)和其他蛋白质组成的动态大分子机器,它催化内含子的切除,成熟为成熟的信使。NTC 以其创始成员酿酒酵母 Prp19 命名,是一种保守的剪接体亚复合物,由至少九个蛋白质组成。在剪接体组装过程中,与 NTC 的稳定结合与活性剪接体的转变相关,尽管 NTC 功能的机制尚不清楚。裂殖酵母 Cdc5 是 NTC 的核心亚基,是剪接前 mRNA 所必需的必需蛋白。高度保守的 Cdc5 N 端含有两个典型的 Myb(髓样白血病)重复序列(R1 和 R2)和第三个结构域(D3),该结构域以前被归类为 Myb 样重复序列。虽然 Cdc5 的 N 端对于其功能是必需的,但 R1、R2 和 D3 如何各自有助于功能尚不清楚。我们使用酵母遗传学、结构方法和 RNA 结合测定的组合,表明 R1、R2 和 D3 对于 Cdc5 在细胞中的功能都是必需的。我们还表明,Cdc5 的 N 端在体外与 RNA 结合。对 Cdc5-D3 的结构和功能分析表明,虽然该结构域不采用 Myb 折叠,但 Cdc5-D3 优先结合双链 RNA。我们的数据表明,Cdc5 的 N 端与拟议位于剪接体催化核心附近的 RNA 结构相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1cb/4204884/79a588e13525/bi-2014-008639_0002.jpg

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