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酿酒酵母Cgr1p在rRNA前体加工和60S核糖体亚基合成中的作用鉴定。

Identification of a role for Saccharomyces cerevisiae Cgr1p in pre-rRNA processing and 60S ribosome subunit synthesis.

作者信息

Moy Terence I, Boettner Douglas, Rhodes Judith C, Silver Pamela A, Askew David S

机构信息

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA2.

University of Cincinnati College of Medicine, Department of Pathology & Laboratory Medicine, Cincinnati, OH 45267-0529, USA1.

出版信息

Microbiology (Reading). 2002 Apr;148(Pt 4):1081-1090. doi: 10.1099/00221287-148-4-1081.

Abstract

Saccharomyces cerevisiae CGR1 encodes a conserved fungal protein that localizes to the nucleolus. To determine if this localization reflects a role for Cgr1p in ribosome biogenesis two yeast cgr1 mutants were examined for defects in ribosome synthesis: a conditional depletion strain in which CGR1 is under the control of a tetracycline-repressible promoter and a mutant strain in which a C-terminal truncated Cgr1p is expressed. Both strains had impaired growth rates and were hypersensitive to the aminoglycosides paromomycin and hygromycin. Polysome analyses of the mutants revealed increased levels of free 40S subunits relative to 60S subunits, a decrease in 80S monosomes and accumulation of half-mer polysomes. Pulse-chase labelling demonstrated that pre-rRNA processing was defective in the mutants, resulting in accumulation of the 35S, 27S and 7S pre-rRNAs and delayed production of the mature 25S and 5 small middle dot8S rRNAs. The synthesis of the 18S and 5S rRNAs was unaffected. Loss of Cgr1 function also caused a partial delocalization of the 5'-ITS1 RNA and the nucleolar protein Nop1p into the nucleoplasm, suggesting that Cgr1p contributes to compartmentalization of nucleolar constituents. Together these findings establish a role for Cgr1p in ribosome biogenesis.

摘要

酿酒酵母CGR1编码一种定位于核仁的保守真菌蛋白。为了确定这种定位是否反映了Cgr1p在核糖体生物合成中的作用,研究人员检测了两个酵母cgr1突变体在核糖体合成方面的缺陷:一个是条件性缺失菌株,其中CGR1受四环素可抑制启动子的控制;另一个是突变菌株,其中表达的是C端截短的Cgr1p。这两种菌株的生长速率均受损,并且对氨基糖苷类药物巴龙霉素和潮霉素高度敏感。对突变体的多核糖体分析显示,相对于60S亚基,游离40S亚基的水平增加,80S单体减少,半聚核糖体积累。脉冲追踪标记表明,突变体中的前体rRNA加工存在缺陷,导致35S、27S和7S前体rRNA积累,成熟的25S和5.8S rRNA产生延迟。18S和5S rRNA的合成未受影响。Cgr1功能的丧失还导致5'-ITS1 RNA和核仁蛋白Nop1p部分定位于核质中,这表明Cgr1p有助于核仁成分的区室化。这些发现共同确立了Cgr1p在核糖体生物合成中的作用。

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