Immobilization of Proteins in the Nucleolus by Ribosomal Intergenic Spacer Noncoding RNA

被引:207
作者
Audas, Timothy E. [1 ,2 ]
Jacob, Mathieu D. [1 ,2 ]
Lee, Stephen [1 ,2 ]
机构
[1] Univ Ottawa, Dept Cellular & Mol Med, Ottawa, ON K1H 8M5, Canada
[2] Univ Ottawa, Fac Med, Ottawa, ON K1H 8M5, Canada
关键词
NUCLEAR; LOCALIZATION; TRANSCRIPTION; MDM2; DNA; SEQUESTRATION; NUCLEOPLASM; ACTIVATION; GRANULES; DYNAMICS;
D O I
10.1016/j.molcel.2011.12.012
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
Cellular pathways are established and maintained by stochastic interactions of highly mobile molecules. The nucleolus plays a central role in the regulation of these molecular networks by capturing and immobilizing proteins. Here, we report a function for non-coding RNA (ncRNA) in the regulation of protein dynamics of key cellular factors, including VHL, Hsp70 and MDM2/PML. Stimuli-specific loci of the nucleolar intergenic spacer produce ncRNA capable of capturing and immobilizing proteins that encode a discrete peptidic code referred to as the nucleolar detention sequence (NoDS). Disruption of the NoDS/intergenic RNA interaction enables proteins to evade nucleolar sequestration and retain their dynamic profiles. Mislocalization of intergenic ncRNA triggers protein immobilization outside of the nucleolus, demonstrating that these ncRNA species can operate independently from the nucleolar architecture. We propose a model whereby protein immobilization by ncRNA is a post-translational regulatory mechanism.
引用
收藏
页码:147 / 157
页数:11
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