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Role of Pre-rRNA Base Pairing and 80S Complex Formation in Subnucleolar Localization of the U3 snoRNP

机译:前rRNA碱基配对和80S复杂形成在U3 snoRNP的亚核定位中的作用。

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摘要

In the nucleolus the U3 snoRNA is recruited to the 80S pre-rRNA processing complex in the dense fibrillar component (DFC). The U3 snoRNA is found throughout the nucleolus and has been proposed to move with the preribosomes to the granular component (GC). In contrast, the localization of other RNAs, such as the U8 snoRNA, is restricted to the DFC. Here we show that the incorporation of the U3 snoRNA into the 80S processing complex is not dependent on pre-rRNA base pairing sequences but requires the B/C motif, a U3-specific protein-binding element. We also show that the binding of Mpp10 to the 80S U3 complex is dependent on sequences within the U3 snoRNA that base pair with the pre-rRNA adjacent to the initial cleavage site. Furthermore, mutations that inhibit 80S complex formation and/or the association of Mpp10 result in retention of the U3 snoRNA in the DFC. From this we propose that the GC localization of the U3 snoRNA is a direct result of its active involvement in the initial steps of ribosome biogenesis.
机译:在核仁中,U3 snoRNA被募集到致密纤维状成分(DFC)中的80S pre-rRNA加工复合体中。 U3 snoRNA被发现存在于整个核仁中,并被提议与核糖体一起移至颗粒成分(GC)。相反,其他RNA(例如U8 snoRNA)的定位仅限于DFC。在这里,我们显示将U3 snoRNA掺入80S加工复合物中并不依赖于rRNA之前的碱基配对序列,而是需要B / C基序,即U3特异性蛋白结合元件。我们还表明,Mpp10与80S U3复合物的结合取决于U3 snoRNA中与邻近初始切割位点的pre-rRNA碱基配对的序列。此外,抑制80S复合物形成和/或Mpp10缔合的突变导致U3 snoRNA保留在DFC中。因此,我们认为U3 snoRNA的GC定位是其积极参与核糖体生物发生的初始步骤的直接结果。

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