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Nat Cell Biol. 2006 Jul;8(7):668-76. doi: 10.1038/ncb1424. Epub 2006 Jun 18.
2
Inositol hexakisphosphate and Gle1 activate the DEAD-box protein Dbp5 for nuclear mRNA export.肌醇六磷酸和Gle1激活DEAD盒蛋白Dbp5以促进核mRNA输出。
Nat Cell Biol. 2006 Jul;8(7):711-6. doi: 10.1038/ncb1427. Epub 2006 Jun 18.
3
The nucleolar protein Esf2 interacts directly with the DExD/H box RNA helicase, Dbp8, to stimulate ATP hydrolysis.核仁蛋白Esf2与DExD/H盒RNA解旋酶Dbp8直接相互作用,以刺激ATP水解。
Nucleic Acids Res. 2006 Jun 13;34(10):3189-99. doi: 10.1093/nar/gkl419. Print 2006.
4
A functional network involved in the recycling of nucleocytoplasmic pre-60S factors.一个参与核质前60S因子循环利用的功能网络。
J Cell Biol. 2006 May 8;173(3):349-60. doi: 10.1083/jcb.200510080. Epub 2006 May 1.
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Proteome survey reveals modularity of the yeast cell machinery.蛋白质组研究揭示酵母细胞机制的模块化特性。
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Ytm1, Nop7, and Erb1 form a complex necessary for maturation of yeast 66S preribosomes.Ytm1、Nop7和Erb1形成了酵母66S前核糖体成熟所必需的复合物。
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The putative NTPase Fap7 mediates cytoplasmic 20S pre-rRNA processing through a direct interaction with Rps14.假定的NTP酶Fap7通过与Rps14直接相互作用介导细胞质20S前体rRNA加工。
Mol Cell Biol. 2005 Dec;25(23):10352-64. doi: 10.1128/MCB.25.23.10352-10364.2005.
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The novel ATP-binding cassette protein ARB1 is a shuttling factor that stimulates 40S and 60S ribosome biogenesis.新型ATP结合盒蛋白ARB1是一种穿梭因子,可刺激40S和60S核糖体的生物合成。
Mol Cell Biol. 2005 Nov;25(22):9859-73. doi: 10.1128/MCB.25.22.9859-9873.2005.
9
Roles of eukaryotic ribosomal proteins in maturation and transport of pre-18S rRNA and ribosome function.真核生物核糖体蛋白在18S前体rRNA成熟与转运及核糖体功能中的作用。
Mol Cell. 2005 Oct 28;20(2):263-75. doi: 10.1016/j.molcel.2005.09.005.
10
The splicing ATPase prp43p is a component of multiple preribosomal particles.剪接ATP酶prp43p是多个前核糖体颗粒的一个组成部分。
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酿酒酵母Npa2p(Urb2p)的特性揭示了一种低分子量复合物,其包含参与60S核糖体亚基生物合成早期步骤的Dbp6p、Npa1p(Urb1p)、Nop8p和Rsa3p。

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.

作者信息

Rosado Iván V, Dez Christophe, Lebaron Simon, Caizergues-Ferrer Michèle, Henry Yves, de la Cruz Jesús

机构信息

Departamento de Genética, Facultad de Biología, Universidad de Sevilla, Avenida Reina Mercedes 6, E-41012 Seville, Spain.

出版信息

Mol Cell Biol. 2007 Feb;27(4):1207-21. doi: 10.1128/MCB.01523-06. Epub 2006 Dec 4.

DOI:10.1128/MCB.01523-06
PMID:17145778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1800719/
Abstract

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.

摘要

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。