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BMAL1 Associates with NOP58 in the Nucleolus and Contributes to Pre-rRNA Processing
被引:18
|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
来源:
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.
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页数:39
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