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A Dynamic Scaffold of Pre-snoRNP Factors Facilitates Human Box C/D snoRNP Assembly

机译:pre-snoRNP因子的动态支架有助于人框C / D snoRNP组装。

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摘要

The box C/D small nucleolar RNPs (snoRNPs) are essential for the processing and modification of rRNA. The core box C/D proteins are restructured during human U3 box C/D snoRNP biogenesis; however, the molecular basis of this is unclear. Here we show that the U8 snoRNP is also restructured, suggesting that this may occur with all box C/D snoRNPs. We have characterized four novel human biogenesis factors (BCD1, NOP17, NUFIP, and TAF9) which, along with the ATPases TIP48 and TIP49, are likely to be involved in the formation of the pre-snoRNP. We have analyzed the in vitro protein-protein interactions between the assembly factors and core box C/D proteins. Surprisingly, this revealed few interactions between the individual core box C/D proteins. However, the novel biogenesis factors and TIP48 and TIP49 interacted with one or more of the core box C/D proteins, implying that they mediate the assembly of the pre-snoRNP. Consistent with this, we show that NUFIP bridges interactions between the core box C/D proteins in a partially reconstituted pre-snoRNP. Restructuring of the core complex probably reflects the conversion of the pre-snoRNP, where core protein-protein interactions are maintained by the bridging biogenesis factors, to the mature snoRNP.
机译:盒式C / D小核仁RNP(snoRNP)对于rRNA的加工和修饰至关重要。核心框C / D蛋白在人类U3框C / D snoRNP生物发生过程中重组。但是,其分子基础尚不清楚。在这里,我们显示U8 snoRNP也已重组,这表明所有盒式C / D snoRNP都可能发生这种情况。我们已经表征了四个新的人类生物发生因子(BCD1,NOP17,NUFIP和TAF9),它们与ATPases TIP48和TIP49一起可能参与了pre-snoRNP的形成。我们已经分析了组装因子和核心框C / D蛋白质之间的体外蛋白质-蛋白质相互作用。出人意料的是,这揭示了单个核心盒C / D蛋白之间几乎没有相互作用。但是,新的生物发生因子以及TIP48和TIP49与一个或多个核心框C / D蛋白相互作用,这意味着它们介导了pre-snoRNP的装配。与此相一致,我们表明NUFIP桥接了部分重组的pre-snoRNP核心盒C / D蛋白之间的相互作用。核心复合物的重组可能反映了pre-snoRNP的转化,在成熟的snoRNP中,核心蛋白之间的相互作用通过桥接生物发生因子得以维持,而snoRNP则在其中。

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