Diverse Regulators of Human Ribosome Biogenesis Discovered by Changes in Nucleolar Number

被引:80
作者
Farley-Barnes, Katherine I. [1 ]
McCann, Kathleen L. [2 ,3 ]
Ogawa, Lisa M. [1 ]
Merkel, Janie [4 ]
Surovtseva, Yulia V. [4 ]
Baserga, Susan J. [1 ,2 ,5 ]
机构
[1] Yale Univ, Sch Med, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
[3] NIEHS, Epigenet & Stem Cell Biol Lab, NIH, POB 12233 MD F3-05, Res Triangle Pk, NC 27709 USA
[4] Yale Univ, Yale Ctr Mol Discovery, 600 West Campus Dr, West Haven, CT 06516 USA
[5] Yale Univ, Dept Therapeut Radiol, Sch Med, New Haven, CT 06520 USA
来源
CELL REPORTS | 2018年 / 22卷 / 07期
关键词
RNA-POLYMERASE-I; TRANSCRIPTION ELONGATION; RDNA TRANSCRIPTION; S6; KINASE; PROTEIN; GENE; P53; TARGET; STRESS; LIN28;
D O I
10.1016/j.celrep.2018.01.056
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ribosome biogenesis is a highly regulated, essential cellular process. Although studies in yeast have established some of the biological principles of ribosome biogenesis, many of the intricacies of its regulation in higher eukaryotes remain unknown. To understand how ribosome biogenesis is globally integrated in human cells, we conducted a genome-wide siRNA screen for regulators of nucleolar number. We found 139 proteins whose depletion changed the number of nucleoli per nucleus from 2-3 to only 1 in human MCF10A cells. Follow-up analyses on 20 hits found many (90%) to be essential for the nucleolar functions of rDNA transcription (7), pre-ribosomal RNA (pre-rRNA) processing (16), and/or global protein synthesis (14). This genome-wide analysis exploits the relationship between nucleolar number and function to discover diverse cellular pathways that regulate the making of ribosomes and paves the way for further exploration of the links between ribosome biogenesis and human disease.
引用
收藏
页码:1923 / 1934
页数:12
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