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Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation
In eukaryotes, the 40 S ribosomal subunit serves as the platform of initiation factor assembly, to place itself precisely on the AUG start codon. Structural arrangement of the 18 S rRNA determines the overall shape of the 40 S subunit. Here, we present genetic evaluation of yeast 18 S rRNA function...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Society for Biochemistry and Molecular Biology
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952221/ https://www.ncbi.nlm.nih.gov/pubmed/20699223 http://dx.doi.org/10.1074/jbc.M110.146662 |
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author | Nemoto, Naoki Singh, Chingakham Ranjit Udagawa, Tsuyoshi Wang, Suzhi Thorson, Elizabeth Winter, Zachery Ohira, Takahiro Ii, Miki Valášek, Leoš Brown, Susan J. Asano, Katsura |
author_facet | Nemoto, Naoki Singh, Chingakham Ranjit Udagawa, Tsuyoshi Wang, Suzhi Thorson, Elizabeth Winter, Zachery Ohira, Takahiro Ii, Miki Valášek, Leoš Brown, Susan J. Asano, Katsura |
author_sort | Nemoto, Naoki |
collection | PubMed |
description | In eukaryotes, the 40 S ribosomal subunit serves as the platform of initiation factor assembly, to place itself precisely on the AUG start codon. Structural arrangement of the 18 S rRNA determines the overall shape of the 40 S subunit. Here, we present genetic evaluation of yeast 18 S rRNA function using 10 point mutations altering the polysome profile. All the mutants reduce the abundance of the mutant 40 S, making it limiting for translation initiation. Two of the isolated mutations, G875A, altering the core of the platform domain that binds eIF1 and eIF2, and A1193U, changing the h31 loop located below the P-site tRNA(i)(Met), show phenotypes indicating defective regulation of AUG selection. Evidence is provided that these mutations reduce the interaction with the components of the preinitiation complex, thereby inhibiting its function at different steps. These results indicate that the 18 S rRNA mutations impair the integrity of scanning-competent preinitiation complex, thereby altering the 40 S subunit response to stringent AUG selection. Interestingly, nine of the mutations alter the body/platform domains of 18 S rRNA, potentially affecting the bridges to the 60 S subunit, but they do not change the level of 18 S rRNA intermediates. Based on these results, we also discuss the mechanism of the selective degradation of the mutant 40 S subunits. |
format | Text |
id | pubmed-2952221 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-29522212010-10-18 Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation Nemoto, Naoki Singh, Chingakham Ranjit Udagawa, Tsuyoshi Wang, Suzhi Thorson, Elizabeth Winter, Zachery Ohira, Takahiro Ii, Miki Valášek, Leoš Brown, Susan J. Asano, Katsura J Biol Chem Protein Synthesis and Degradation In eukaryotes, the 40 S ribosomal subunit serves as the platform of initiation factor assembly, to place itself precisely on the AUG start codon. Structural arrangement of the 18 S rRNA determines the overall shape of the 40 S subunit. Here, we present genetic evaluation of yeast 18 S rRNA function using 10 point mutations altering the polysome profile. All the mutants reduce the abundance of the mutant 40 S, making it limiting for translation initiation. Two of the isolated mutations, G875A, altering the core of the platform domain that binds eIF1 and eIF2, and A1193U, changing the h31 loop located below the P-site tRNA(i)(Met), show phenotypes indicating defective regulation of AUG selection. Evidence is provided that these mutations reduce the interaction with the components of the preinitiation complex, thereby inhibiting its function at different steps. These results indicate that the 18 S rRNA mutations impair the integrity of scanning-competent preinitiation complex, thereby altering the 40 S subunit response to stringent AUG selection. Interestingly, nine of the mutations alter the body/platform domains of 18 S rRNA, potentially affecting the bridges to the 60 S subunit, but they do not change the level of 18 S rRNA intermediates. Based on these results, we also discuss the mechanism of the selective degradation of the mutant 40 S subunits. American Society for Biochemistry and Molecular Biology 2010-10-15 2010-08-10 /pmc/articles/PMC2952221/ /pubmed/20699223 http://dx.doi.org/10.1074/jbc.M110.146662 Text en © 2010 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) applies to Author Choice Articles |
spellingShingle | Protein Synthesis and Degradation Nemoto, Naoki Singh, Chingakham Ranjit Udagawa, Tsuyoshi Wang, Suzhi Thorson, Elizabeth Winter, Zachery Ohira, Takahiro Ii, Miki Valášek, Leoš Brown, Susan J. Asano, Katsura Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation |
title | Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation |
title_full | Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation |
title_fullStr | Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation |
title_full_unstemmed | Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation |
title_short | Yeast 18 S rRNA Is Directly Involved in the Ribosomal Response to Stringent AUG Selection during Translation Initiation |
title_sort | yeast 18 s rrna is directly involved in the ribosomal response to stringent aug selection during translation initiation |
topic | Protein Synthesis and Degradation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952221/ https://www.ncbi.nlm.nih.gov/pubmed/20699223 http://dx.doi.org/10.1074/jbc.M110.146662 |
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