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A second riboswitch class for the enzyme cofactor NAD(+)

A bacterial noncoding RNA motif almost exclusively associated with pnuC genes was uncovered using comparative sequence analysis. Some PnuC proteins are known to transport nicotinamide riboside (NR), which is a component of the ubiquitous and abundant enzyme cofactor nicotinamide adenine dinucleotide...

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Detalles Bibliográficos
Autores principales: Panchapakesan, Shanker S.S., Corey, Lukas, Malkowski, Sarah N., Higgs, Gadareth, Breaker, Ronald R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749635/
https://www.ncbi.nlm.nih.gov/pubmed/33087526
http://dx.doi.org/10.1261/rna.077891.120
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author Panchapakesan, Shanker S.S.
Corey, Lukas
Malkowski, Sarah N.
Higgs, Gadareth
Breaker, Ronald R.
author_facet Panchapakesan, Shanker S.S.
Corey, Lukas
Malkowski, Sarah N.
Higgs, Gadareth
Breaker, Ronald R.
author_sort Panchapakesan, Shanker S.S.
collection PubMed
description A bacterial noncoding RNA motif almost exclusively associated with pnuC genes was uncovered using comparative sequence analysis. Some PnuC proteins are known to transport nicotinamide riboside (NR), which is a component of the ubiquitous and abundant enzyme cofactor nicotinamide adenine dinucleotide (NAD(+)). Thus, we speculated that the newly found “pnuC motif” RNAs might function as aptamers for a novel class of NAD(+)-sensing riboswitches. RNA constructs that encompass the conserved nucleotides and secondary structure features that define the motif indeed selectively bind NAD(+), nicotinamide mononucleotide (NMN), and NR. Mutations that disrupt strictly conserved nucleotides of the aptamer also disrupt ligand binding. These bioinformatic and biochemical findings indicate that pnuC motif RNAs are likely members of a second riboswitch class that regulates gene expression in response to NAD(+) binding.
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spelling pubmed-77496352021-01-01 A second riboswitch class for the enzyme cofactor NAD(+) Panchapakesan, Shanker S.S. Corey, Lukas Malkowski, Sarah N. Higgs, Gadareth Breaker, Ronald R. RNA Article A bacterial noncoding RNA motif almost exclusively associated with pnuC genes was uncovered using comparative sequence analysis. Some PnuC proteins are known to transport nicotinamide riboside (NR), which is a component of the ubiquitous and abundant enzyme cofactor nicotinamide adenine dinucleotide (NAD(+)). Thus, we speculated that the newly found “pnuC motif” RNAs might function as aptamers for a novel class of NAD(+)-sensing riboswitches. RNA constructs that encompass the conserved nucleotides and secondary structure features that define the motif indeed selectively bind NAD(+), nicotinamide mononucleotide (NMN), and NR. Mutations that disrupt strictly conserved nucleotides of the aptamer also disrupt ligand binding. These bioinformatic and biochemical findings indicate that pnuC motif RNAs are likely members of a second riboswitch class that regulates gene expression in response to NAD(+) binding. Cold Spring Harbor Laboratory Press 2021-01 /pmc/articles/PMC7749635/ /pubmed/33087526 http://dx.doi.org/10.1261/rna.077891.120 Text en © 2021 Panchapakesan et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society http://creativecommons.org/licenses/by/4.0/ This article, published in RNA, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Panchapakesan, Shanker S.S.
Corey, Lukas
Malkowski, Sarah N.
Higgs, Gadareth
Breaker, Ronald R.
A second riboswitch class for the enzyme cofactor NAD(+)
title A second riboswitch class for the enzyme cofactor NAD(+)
title_full A second riboswitch class for the enzyme cofactor NAD(+)
title_fullStr A second riboswitch class for the enzyme cofactor NAD(+)
title_full_unstemmed A second riboswitch class for the enzyme cofactor NAD(+)
title_short A second riboswitch class for the enzyme cofactor NAD(+)
title_sort second riboswitch class for the enzyme cofactor nad(+)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749635/
https://www.ncbi.nlm.nih.gov/pubmed/33087526
http://dx.doi.org/10.1261/rna.077891.120
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