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PMID: 17245450 Published · epublish English Journal Article Research Support, N.I.H., Extramural

Optimization of ribosome structure and function by rRNA base modification.

PloS one ·Vol. 2 ·No. 1 ·2007-01-24 ·Pages e174

Baxter-Roshek JL, Petrov AN, Dinman JD

Abstract

Translating mRNA sequences into functional proteins is a fundamental process necessary for the viability of organisms throughout all kingdoms of life. The ribosome carries out this process with a delicate balance between speed and accuracy. This work investigates how ribosome structure and function are affected by rRNA base modification. The prevailing view is that rRNA base modifications serve to fine tune ribosome structure and function. To test this hypothesis, yeast strains deficient in rRNA modifications in the ribosomal peptidyltransferase center were monitored for changes in and translational fidelity. These studies revealed allele-specific sensitivity to translational inhibitors, changes in reading frame maintenance, nonsense suppression and aa-tRNA selection. Ribosomes isolated from two mutants with the most pronounced phenotypic changes had increased affinities for aa-tRNA, and surprisingly, increased rates of peptidyltransfer as monitored by the puromycin assay. rRNA chemical analyses of one of these mutants identified structural changes in five specific bases associated with the ribosomal A-site. Together, the data suggest that modification of these bases fine tune the structure of the A-site region of the large subunit so as to assure correct positioning of critical rRNA bases involved in aa-tRNA accommodation into the PTC, of the eEF-1A.aa-tRNA.GTP ternary complex with the GTPase associated center, and of the aa-tRNA in the A-site. These findings represent a direct demonstration in support of the prevailing hypothesis that rRNA modifications serve to optimize rRNA structure for production of accurate and efficient ribosomes.

MeSH Terms
Alleles Base Sequence Humans Models, Molecular Molecular Sequence Data Mutation Nucleic Acid Conformation Peptidyl Transferases/chemistry,genetics Protein Biosynthesis Protein Conformation RNA, Ribosomal/chemistry,genetics RNA, Transfer, Amino Acid-Specific/chemistry,genetics Ribosome Subunits, Large, Eukaryotic/chemistry,genetics Ribosomes/chemistry,genetics
Chemicals
RNA, Ribosomal RNA, Transfer, Amino Acid-Specific Peptidyl Transferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Baxter-Roshek Jennifer L
Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland, United States of America.
Petrov Alexey N
Dinman Jonathan D
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2007-01-24
Epub
2007-00-24
Pages
e174
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC1766470
Subset
IM
Grants
NIGMS NIH HHS · R01 GM058859 · United States
NIAID NIH HHS · T32 AI051967 · United States
NIGMS NIH HHS · R01 GM58859 · United States
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