Cic1p/Nsa3p is required for synthesis and nuclear export of 60S ribosomal subunits

被引:35
作者
Fatica, A [1 ]
Oeffinger, M
Tollervey, D
Bozzoni, I
机构
[1] Univ Roma La Sapienza, Dept Genet & Mol Biol, Rome, Italy
[2] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh, Midlothian, Scotland
关键词
pre-rRNA; ribosome synthesis;
D O I
10.1261/rna.5130503
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cic1p/Nsa3p was previously reported to be associated with the 26S proteasome and required for the degradation of specific substrates, but was also shown to be associated with early pre-60S particles and to be localized to the nucleolus. Here we report that Cic1p/Nsa3p is required for the synthesis of 60S ribosome subunits. A temperature-sensitive lethal cic1-2 point mutation inhibits synthesis of the mature 5.8S and 25S rRNAs. Release of the pre-60S particles from the nucleolus to the nucleoplasm was also inhibited as judged by the nuclear accumulation of an Rpl11b-GFP reporter construct. We suggest that Cic1p/Nsa3p associates early with nascent preribosomal particles and is required for correct processing and nuclear release of large ribosomal subunit precursors.
引用
收藏
页码:1431 / 1436
页数:6
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