BMAL1 Associates with NOP58 in the Nucleolus and Contributes to Pre-rRNA Processing

被引:19
作者
Cervantes, Marlene [1 ]
Forne, Ignasi [2 ]
Ranjit, Suman [3 ,4 ]
Gratton, Enrico [3 ]
Imhof, Axel [2 ]
Sassone-Corsi, Paolo [1 ]
机构
[1] Univ Calif Irvine, Dept Biol Chem, Ctr Epigenet & Metab, U1233 INSERM, Irvine, CA 92697 USA
[2] Ludwig Maximilian Univ Munich, Biomed Ctr, Prot Anal Unit, D-80539 Munich, Germany
[3] Univ Calif Irvine, Dept Biomed Engn, Lab Fluorescence Dynam, Irvine, CA 92697 USA
[4] Georgetown Univ, Dept Biochem & Mol & Cellular Biol, Washington, DC 20057 USA
基金
美国国家卫生研究院;
关键词
CIRCADIAN CLOCK; BOX C/D; BIOGENESIS; TRANSCRIPTION; LOCALIZATION; GENES; U3; PHOSPHORYLATION; DEACETYLATION; METABOLISM;
D O I
10.1016/j.isci.2020.101151
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The transcription factor BMAL1 is a core element of the circadian clock that contributes to cyclic control of genes transcribed by RNA polymerase II. By using biochemical cellular fractionation and immunofluorescence analyses we reveal a previously uncharacterized nucleolar localization for BMAL1. We used an unbiased approach to determine the BMAL1 interactome by mass spectrometry and identified NOP58 as a prominent nucleolar interactor. NOP58, a core component of the box C/D small nucleolar ribonucleoprotein complex, associates with Snord118 to control specific pre-ribosomal RNA (pre-rRNA) processing steps. These results suggest a non- canonical role of BMAL1 in ribosomal RNA regulation. Indeed, we show that BMAL1 controls NOP58-associated Snord118 nucleolar levels and cleavage of unique pre-rRNA intermediates. Our findings identify an unsuspected function of BMAL1 in the nucleolus that appears distinct from its canonical role in the circadian clock system.
引用
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页数:39
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