Rosado Iván V, Dez Christophe, Lebaron Simon, Caizergues-Ferrer Michèle, Henry Yves, de la Cruz Jesús
Departamento de Genética, Facultad de Biología, Universidad de Sevilla, Avenida Reina Mercedes 6, E-41012 Seville, Spain.
Mol Cell Biol. 2007 Feb;27(4):1207-21. doi: 10.1128/MCB.01523-06. Epub 2006 Dec 4.
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 27SA(2) 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.
我们报道了酵母Npa2p(Urb2p)蛋白的特性,该蛋白对60S核糖体亚基的生物合成至关重要。我们在与rsa3无效等位基因的合成致死筛选中鉴定出了这种蛋白。Rsa3p是推定的RNA解旋酶Dbp6p的遗传伙伴。Npa2p的突变或缺失会导致60S亚基净减少,以及所有27S前体rRNA和成熟25S及5.8S rRNA水平下降。这可能是由于早期60S前体颗粒的不稳定性所致。与Npa2p在60S亚基生物合成中的作用一致,绿色荧光蛋白标记的Npa2p主要定位于核仁,TAP标记的Npa2p在蔗糖梯度中与大复合物一起沉降,并且主要与含有27SA(2)前体rRNA的前核糖体颗粒相关。此外,我们揭示了Npa2p、60S亚基生物合成早期步骤所需的几个因子(Dbp6p、Dbp7p、Dbp9p、Npa1p、Nop8p和Rsa3p)以及60S蛋白Rpl3p之间的遗传合成相互作用。此外,免疫共沉淀和凝胶过滤分析表明,至少Npa2p、Dbp6p、Npa1p、Nop8p和Rsa3p共同存在于一个低分子量的亚复合物中,其完整性与RNA无关。我们的结果支持了这五个因子在60S亚基生物合成早期步骤中协同工作的观点。