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首页> 外文期刊>Molecular and Cellular Biology >Characterization of Saccharomyces cerevisiae Npa2p (Urb2p) Reveals a Low-Molecular-Mass Complex Containing Dbp6p, Npa1p (Urb1p), Nop8p, and Rsa3p Involved in Early Steps of 60S Ribosomal Subunit Biogenesis
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Characterization of Saccharomyces cerevisiae Npa2p (Urb2p) Reveals a Low-Molecular-Mass Complex Containing Dbp6p, Npa1p (Urb1p), Nop8p, and Rsa3p Involved in Early Steps of 60S Ribosomal Subunit Biogenesis

机译:酿酒酵母Npa2p(Urb2p)的表征揭示了涉及Dbp6p,Npa1p(Urb1p),Nop8p和Rsa3p的低分子质量复合物,参与了60S核糖体亚基生物发生的早期步骤。

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摘要

We report the characterization of the yeast Npa2p (Urb2p) protein, which is essential for 60S ribosomal subunit biogenesis. We identified this protein in a synthetic lethal screening with the rsa3 null allele. Rsa3p is a genetic partner of the putative RNA helicase Dbp6p. Mutation or depletion of Npa2p leads to a net deficit in 60S subunits and a decrease in the levels all 27S pre-rRNAs and mature 25S and 5.8S rRNAs. This is likely due to instability of early pre-60S particles. Consistent with a role of Npa2p in 60S subunit biogenesis, green fluorescent protein-tagged Npa2p localizes predominantly to the nucleolus and TAP-tagged Npa2p sediments with large complexes in sucrose gradients and is associated mainly with 27SA2 pre-rRNA-containing preribosomal particles. In addition, we reveal a genetic synthetic interaction between Npa2p, several factors required for early steps of 60S subunit biogenesis (Dbp6p, Dbp7p, Dbp9p, Npa1p, Nop8p, and Rsa3p), and the 60S protein Rpl3p. Furthermore, coimmunoprecipitation and gel filtration analyses demonstrated that at least Npa2p, Dbp6p, Npa1p, Nop8p, and Rsa3p are present together in a subcomplex of low molecular mass whose integrity is independent of RNA. Our results support the idea that these five factors work in concert during the early steps of 60S subunit biogenesis.
机译:我们报告了酵母Npa2p(Urb2p)蛋白的特征,这对于60S核糖体亚基生物发生至关重要。我们在合成致死性筛选中与 rsa3 空等位基因鉴定了这种蛋白质。 Rsa3p是推定的RNA解旋酶Dbp6p的遗传伴侣。 Npa2p的突变或耗竭会导致60S亚基的净缺失,并降低所有27S pre-rRNA和成熟的25S和5.8S rRNA的水平。这可能是由于60S之前的早期颗粒不稳定。与Npa2p在60S亚基生物发生中的作用一致,绿色荧光蛋白标记的Npa2p主要定位于核糖和TAP标签的Npa2p沉积物,蔗糖梯度中具有大的复合物,并且主要与27SA 2 前-含rRNA的核糖体前颗粒。此外,我们揭示了Npa2p,60S亚基生物发生的早期步骤所需的几个因素(Dbp6p,Dbp7p,Dbp9p,Npa1p,Nop8p和Rsa3p)与60S蛋白Rpl3p之间的遗传合成相互作用。此外,共免疫沉淀和凝胶过滤分析表明,至少Npa2p,Dbp6p,Npa1p,Nop8p和Rsa3p共同存在于低分子量亚复合物中,其完整性独立于RNA。我们的结果支持以下观点:这五个因素在60S亚基生物发生的早期阶段协同作用。

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