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Box C/D small nucleolar RNA trafficking involves small nucleolar RNP proteins nucleolar factors and a novel nuclear domain

机译:Box C / D小核仁RNA贩运涉及小核仁RNP蛋白核仁因子和新型核域

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摘要

Nucleolar localization of box C/D small nucleolar (sno) RNAs requires the box C/D motif and, in vertebrates, involves transit through Cajal bodies (CB). We report that in yeast, overexpression of a box C/D reporter leads to a block in the localization pathway with snoRNA accumulation in a specific sub-nucleolar structure, the nucleolar body (NB). The human survival of motor neuron protein (SMN), a marker of gems/CB, specifically localizes to the NB when expressed in yeast, supporting similarities between these structures. Box C/D snoRNA accumulation in the NB was decreased by mutation of Srp40 and increased by mutation of Nsr1p, two related nucleolar proteins that are homologous to human Nopp140 and nucleolin, respectively. Box C/D snoRNAs also failed to accumulate in the NB, and became delocalized to the nucleoplasm, upon depletion of any of the core snoRNP proteins, Nop1p/fibrillarin, Snu13p, Nop56p and Nop5p/Nop58p. We conclude that snoRNP assembly occurs either in the nucleoplasm, or during transit of snoRNAs through the NB, followed by routing of the complete snoRNP to functional sites of ribosome synthesis.
机译:盒C / D小核仁(sno)RNA的核仁定位需要盒C / D基序,并且在脊椎动物中涉及通过Cajal体(CBal)的转运。我们报道在酵母中,框C / D报告基因的过度表达导致snoRNA积累在特定亚核仁结构(核仁体(NB))中的定位途径受阻。运动神经元蛋白(SMN)(gems / CB的标记物)的人类存活在酵母中表达时特异性地定位于NB,从而支持了这些结构之间的相似性。 Box的C / D snoRNA在NB中的积累因Srp40的突变而减少,而因Nsr1p的突变而增加,Nsr1p是分别与人Nopp140和nucleolin同源的两个相关核仁蛋白。 Box C / D snoRNAs也未能在NB中积累,并在耗尽任何核心snoRNP蛋白,Nop1p /原纤维蛋白,Snu13p,Nop56p和Nop5p / Nop58p时脱离到核质中。我们得出的结论是,snoRNP组装发生在核质中,或在snoRNAs通过NB转运的过程中,随后将完整的snoRNP路由至核糖体合成的功能位点。

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