共 226 条
Powering through ribosome assembly
被引:157
作者:
Strunk, Bethany S.
[2
]
Karbstein, Katrin
[1
,2
,3
]
机构:
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Chem Biol Doctoral Program, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
来源:
关键词:
ATPase;
GTPase;
quality control;
rRNA processing;
ribosome assembly;
PUTATIVE RNA HELICASE;
YEAST SACCHAROMYCES-CEREVISIAE;
SMALL NUCLEOLAR RNA;
DEAD-BOX PROTEINS;
SMALL NUCLEAR-RNA;
COMPREHENSIVE MUTATIONAL ANALYSIS;
ESCHERICHIA-COLI RIBOSOMES;
POLYMERASE-I TRANSCRIPTION;
EXPANSION SEGMENTS ES3;
GTP-BINDING PROTEIN;
D O I:
10.1261/rna.1792109
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:
Ribosome assembly is required for cell growth in all organisms. Classic in vitro work in bacteria has led to a detailed understanding of the biophysical, thermodynamic, and structural basis for the ordered and correct assembly of ribosomal proteins on ribosomal RNA. Furthermore, it has enabled reconstitution of active subunits from ribosomal RNA and proteins in vitro. Nevertheless, recent work has shown that eukaryotic ribosome assembly requires a large macromolecular machinery in vivo. Many of these assembly factors such as ATPases, GTPases, and kinases hydrolyze nucleotide triphosphates. Because these enzymes are likely regulatory proteins, much work to date has focused on understanding their role in the assembly process. Here, we review these factors, as well as other sources of energy, and their roles in the ribosome assembly process. In addition, we propose roles of energy-releasing enzymes in the assembly process, to explain why energy is used for a process that occurs largely spontaneously in bacteria. Finally, we use literature data to suggest testable models for how these enzymes could be used as targets for regulation of ribosome assembly.
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页码:2083 / 2104
页数:22
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