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A metastable rRNA junction essential for bacterial 30S biogenesis

Tertiary sequence motifs encode interactions between RNA helices that create the three-dimensional structures of ribosomal subunits. A Right Angle motif at the junction between 16S helices 5 and 6 (J5/6) is universally conserved amongst small subunit rRNAs and forms a stable right angle in minimal R...

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Autores principales: Sharma, Indra Mani, Rappé, Mollie C, Addepalli, Balasubrahmanyam, Grabow, Wade W, Zhuang, Zhuoyun, Abeysirigunawardena, Sanjaya C, Limbach, Patrick A, Jaeger, Luc, Woodson, Sarah A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007441/
https://www.ncbi.nlm.nih.gov/pubmed/29850893
http://dx.doi.org/10.1093/nar/gky120
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author Sharma, Indra Mani
Rappé, Mollie C
Addepalli, Balasubrahmanyam
Grabow, Wade W
Zhuang, Zhuoyun
Abeysirigunawardena, Sanjaya C
Limbach, Patrick A
Jaeger, Luc
Woodson, Sarah A
author_facet Sharma, Indra Mani
Rappé, Mollie C
Addepalli, Balasubrahmanyam
Grabow, Wade W
Zhuang, Zhuoyun
Abeysirigunawardena, Sanjaya C
Limbach, Patrick A
Jaeger, Luc
Woodson, Sarah A
author_sort Sharma, Indra Mani
collection PubMed
description Tertiary sequence motifs encode interactions between RNA helices that create the three-dimensional structures of ribosomal subunits. A Right Angle motif at the junction between 16S helices 5 and 6 (J5/6) is universally conserved amongst small subunit rRNAs and forms a stable right angle in minimal RNAs. J5/6 does not form a right angle in the mature ribosome, suggesting that this motif encodes a metastable structure needed for ribosome biogenesis. In this study, J5/6 mutations block 30S ribosome assembly and 16S maturation in Escherichia coli. Folding assays and in-cell X-ray footprinting showed that J5/6 mutations favor an assembly intermediate of the 16S 5′ domain and prevent formation of the central pseudoknot. Quantitative mass spectrometry revealed that mutant pre-30S ribosomes lack protein uS12 and are depleted in proteins uS5 and uS2. Together, these results show that impaired folding of the J5/6 right angle prevents the establishment of inter-domain interactions, resulting in global collapse of the 30S structure observed in electron micrographs of mutant pre-30S ribosomes. We propose that the J5/6 motif is part of a spine of RNA helices that switch conformation at distinct stages of assembly, linking peripheral domains with the 30S active site to ensure the integrity of 30S biogenesis.
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spelling pubmed-60074412018-07-05 A metastable rRNA junction essential for bacterial 30S biogenesis Sharma, Indra Mani Rappé, Mollie C Addepalli, Balasubrahmanyam Grabow, Wade W Zhuang, Zhuoyun Abeysirigunawardena, Sanjaya C Limbach, Patrick A Jaeger, Luc Woodson, Sarah A Nucleic Acids Res RNA and RNA-protein complexes Tertiary sequence motifs encode interactions between RNA helices that create the three-dimensional structures of ribosomal subunits. A Right Angle motif at the junction between 16S helices 5 and 6 (J5/6) is universally conserved amongst small subunit rRNAs and forms a stable right angle in minimal RNAs. J5/6 does not form a right angle in the mature ribosome, suggesting that this motif encodes a metastable structure needed for ribosome biogenesis. In this study, J5/6 mutations block 30S ribosome assembly and 16S maturation in Escherichia coli. Folding assays and in-cell X-ray footprinting showed that J5/6 mutations favor an assembly intermediate of the 16S 5′ domain and prevent formation of the central pseudoknot. Quantitative mass spectrometry revealed that mutant pre-30S ribosomes lack protein uS12 and are depleted in proteins uS5 and uS2. Together, these results show that impaired folding of the J5/6 right angle prevents the establishment of inter-domain interactions, resulting in global collapse of the 30S structure observed in electron micrographs of mutant pre-30S ribosomes. We propose that the J5/6 motif is part of a spine of RNA helices that switch conformation at distinct stages of assembly, linking peripheral domains with the 30S active site to ensure the integrity of 30S biogenesis. Oxford University Press 2018-06-01 2018-02-23 /pmc/articles/PMC6007441/ /pubmed/29850893 http://dx.doi.org/10.1093/nar/gky120 Text en © The Author(s) 2018. 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, Indra Mani
Rappé, Mollie C
Addepalli, Balasubrahmanyam
Grabow, Wade W
Zhuang, Zhuoyun
Abeysirigunawardena, Sanjaya C
Limbach, Patrick A
Jaeger, Luc
Woodson, Sarah A
A metastable rRNA junction essential for bacterial 30S biogenesis
title A metastable rRNA junction essential for bacterial 30S biogenesis
title_full A metastable rRNA junction essential for bacterial 30S biogenesis
title_fullStr A metastable rRNA junction essential for bacterial 30S biogenesis
title_full_unstemmed A metastable rRNA junction essential for bacterial 30S biogenesis
title_short A metastable rRNA junction essential for bacterial 30S biogenesis
title_sort metastable rrna junction essential for bacterial 30s biogenesis
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007441/
https://www.ncbi.nlm.nih.gov/pubmed/29850893
http://dx.doi.org/10.1093/nar/gky120
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