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Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal
In bacteria, the assembly factors tightly orchestrate the maturation of ribosomes whose competency for protein synthesis is validated by translation machinery at various stages of translation cycle. However, what transpires to the quality control measures when the ribosomes are produced with assembl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868393/ https://www.ncbi.nlm.nih.gov/pubmed/31586395 http://dx.doi.org/10.1093/nar/gkz825 |
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author | Sharma, Himanshu Anand, B |
author_facet | Sharma, Himanshu Anand, B |
author_sort | Sharma, Himanshu |
collection | PubMed |
description | In bacteria, the assembly factors tightly orchestrate the maturation of ribosomes whose competency for protein synthesis is validated by translation machinery at various stages of translation cycle. However, what transpires to the quality control measures when the ribosomes are produced with assembly defects remains enigmatic. In Escherichia coli, we show that 30S ribosomes that harbour assembly defects due to the lack of assembly factors such as RbfA and KsgA display suboptimal initiation codon recognition and bypass the critical codon–anticodon proofreading steps during translation initiation. These premature ribosomes on entering the translation cycle compromise the fidelity of decoding that gives rise to errors during initiation and elongation. We show that the assembly defects compromise the binding of initiation factor 3 (IF3), which in turn appears to license the rapid transition of 30S (pre) initiation complex to 70S initiation complex by tempering the validation of codon–anticodon interaction during translation initiation. This suggests that the premature ribosomes harbouring the assembly defects subvert the IF3 mediated proofreading of cognate initiation codon to enter the translation cycle. |
format | Online Article Text |
id | pubmed-6868393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68683932019-11-27 Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal Sharma, Himanshu Anand, B Nucleic Acids Res RNA and RNA-protein complexes In bacteria, the assembly factors tightly orchestrate the maturation of ribosomes whose competency for protein synthesis is validated by translation machinery at various stages of translation cycle. However, what transpires to the quality control measures when the ribosomes are produced with assembly defects remains enigmatic. In Escherichia coli, we show that 30S ribosomes that harbour assembly defects due to the lack of assembly factors such as RbfA and KsgA display suboptimal initiation codon recognition and bypass the critical codon–anticodon proofreading steps during translation initiation. These premature ribosomes on entering the translation cycle compromise the fidelity of decoding that gives rise to errors during initiation and elongation. We show that the assembly defects compromise the binding of initiation factor 3 (IF3), which in turn appears to license the rapid transition of 30S (pre) initiation complex to 70S initiation complex by tempering the validation of codon–anticodon interaction during translation initiation. This suggests that the premature ribosomes harbouring the assembly defects subvert the IF3 mediated proofreading of cognate initiation codon to enter the translation cycle. Oxford University Press 2019-12-02 2019-10-05 /pmc/articles/PMC6868393/ /pubmed/31586395 http://dx.doi.org/10.1093/nar/gkz825 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | RNA and RNA-protein complexes Sharma, Himanshu Anand, B Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal |
title | Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal |
title_full | Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal |
title_fullStr | Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal |
title_full_unstemmed | Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal |
title_short | Ribosome assembly defects subvert initiation Factor3 mediated scrutiny of bona fide start signal |
title_sort | ribosome assembly defects subvert initiation factor3 mediated scrutiny of bona fide start signal |
topic | RNA and RNA-protein complexes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868393/ https://www.ncbi.nlm.nih.gov/pubmed/31586395 http://dx.doi.org/10.1093/nar/gkz825 |
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