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Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes

BACKGROUND: Structured noncoding RNAs perform many functions that are essential for protein synthesis, RNA processing, and gene regulation. Structured RNAs can be detected by comparative genomics, in which homologous sequences are identified and inspected for mutations that conserve RNA secondary st...

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Autores principales: Weinberg, Zasha, Wang, Joy X, Bogue, Jarrod, Yang, Jingying, Corbino, Keith, Moy, Ryan H, Breaker, Ronald R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864571/
https://www.ncbi.nlm.nih.gov/pubmed/20230605
http://dx.doi.org/10.1186/gb-2010-11-3-r31
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author Weinberg, Zasha
Wang, Joy X
Bogue, Jarrod
Yang, Jingying
Corbino, Keith
Moy, Ryan H
Breaker, Ronald R
author_facet Weinberg, Zasha
Wang, Joy X
Bogue, Jarrod
Yang, Jingying
Corbino, Keith
Moy, Ryan H
Breaker, Ronald R
author_sort Weinberg, Zasha
collection PubMed
description BACKGROUND: Structured noncoding RNAs perform many functions that are essential for protein synthesis, RNA processing, and gene regulation. Structured RNAs can be detected by comparative genomics, in which homologous sequences are identified and inspected for mutations that conserve RNA secondary structure. RESULTS: By applying a comparative genomics-based approach to genome and metagenome sequences from bacteria and archaea, we identified 104 candidate structured RNAs and inferred putative functions for many of these. Twelve candidate metabolite-binding RNAs were identified, three of which were validated, including one reported herein that binds the coenzyme S-adenosylmethionine. Newly identified cis-regulatory RNAs are implicated in photosynthesis or nitrogen regulation in cyanobacteria, purine and one-carbon metabolism, stomach infection by Helicobacter, and many other physiological processes. A candidate riboswitch termed crcB is represented in both bacteria and archaea. Another RNA motif may control gene expression from 3'-untranslated regions of mRNAs, which is unusual for bacteria. Many noncoding RNAs that likely act in trans are also revealed, and several of the noncoding RNA candidates are found mostly or exclusively in metagenome DNA sequences. CONCLUSIONS: This work greatly expands the variety of highly structured noncoding RNAs known to exist in bacteria and archaea and provides a starting point for biochemical and genetic studies needed to validate their biologic functions. Given the sustained rate of RNA discovery over several similar projects, we expect that far more structured RNAs remain to be discovered from bacterial and archaeal organisms.
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spelling pubmed-28645712010-05-05 Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes Weinberg, Zasha Wang, Joy X Bogue, Jarrod Yang, Jingying Corbino, Keith Moy, Ryan H Breaker, Ronald R Genome Biol Research BACKGROUND: Structured noncoding RNAs perform many functions that are essential for protein synthesis, RNA processing, and gene regulation. Structured RNAs can be detected by comparative genomics, in which homologous sequences are identified and inspected for mutations that conserve RNA secondary structure. RESULTS: By applying a comparative genomics-based approach to genome and metagenome sequences from bacteria and archaea, we identified 104 candidate structured RNAs and inferred putative functions for many of these. Twelve candidate metabolite-binding RNAs were identified, three of which were validated, including one reported herein that binds the coenzyme S-adenosylmethionine. Newly identified cis-regulatory RNAs are implicated in photosynthesis or nitrogen regulation in cyanobacteria, purine and one-carbon metabolism, stomach infection by Helicobacter, and many other physiological processes. A candidate riboswitch termed crcB is represented in both bacteria and archaea. Another RNA motif may control gene expression from 3'-untranslated regions of mRNAs, which is unusual for bacteria. Many noncoding RNAs that likely act in trans are also revealed, and several of the noncoding RNA candidates are found mostly or exclusively in metagenome DNA sequences. CONCLUSIONS: This work greatly expands the variety of highly structured noncoding RNAs known to exist in bacteria and archaea and provides a starting point for biochemical and genetic studies needed to validate their biologic functions. Given the sustained rate of RNA discovery over several similar projects, we expect that far more structured RNAs remain to be discovered from bacterial and archaeal organisms. BioMed Central 2010 2010-03-15 /pmc/articles/PMC2864571/ /pubmed/20230605 http://dx.doi.org/10.1186/gb-2010-11-3-r31 Text en Copyright ©2010 Weinberg et al.; licensee BioMed Central, Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Weinberg, Zasha
Wang, Joy X
Bogue, Jarrod
Yang, Jingying
Corbino, Keith
Moy, Ryan H
Breaker, Ronald R
Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
title Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
title_full Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
title_fullStr Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
title_full_unstemmed Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
title_short Comparative genomics reveals 104 candidate structured RNAs from bacteria, archaea, and their metagenomes
title_sort comparative genomics reveals 104 candidate structured rnas from bacteria, archaea, and their metagenomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864571/
https://www.ncbi.nlm.nih.gov/pubmed/20230605
http://dx.doi.org/10.1186/gb-2010-11-3-r31
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