Evidence map›Paper›PMID 16086852›Full record

ArticleGenome biology2005

Evidence for a second class of S-adenosylmethionine riboswitches and other regulatory RNA motifs in alpha-proteobacteria.

Keith A Corbino, Jeffrey E Barrick, Jinsoo Lim, Rüdiger Welz, Brian J Tucker, Izabela Puskarz, Maumita Mandal, Noam D Rudnick, Ronald R Breaker

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
7.4field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

127 citing papers in PubMed, 236 citations in OpenAlex.

  1. A cooperative effect of ligands, MgThe Journal of biological chemistry · 2026
    Article
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  5. Review
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  9. The current riboswitch landscape inMicrobiology (Reading, England) · 2024
    Review
  10. Biomolecules · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Discovering riboswitches: the past and the future.Trends in biochemical sciences · 2023
    Review
  16. Variants of the guanine riboswitch class exhibit altered ligand specificities for xanthine, guanine, or 2'-deoxyguanosine.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Review

67 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Keith A CorbinoDepartment of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520-8103, USA. keith.corbino@yale.edu
Jeffrey E Barrick
Jinsoo Lim
Rüdiger Welz
Brian J Tucker
Izabela Puskarz
Maumita Mandal
Noam D Rudnick
Ronald R Breaker
Yale University · USUniversity of California, Berkeley · US

Funding

Natural mRNA Genetic Switches that Bind MetabolitesR01GM068819 · NIGMS · YALE UNIVERSITY · PI BREAKER, RONALD R · 2003 to 2006
$1.3M
NIGMS NIH HHS GM 068819NIGMS NIH HHS R01 GM068819
6 · The paper itself

Abstract

backgroundRiboswitches are RNA elements in the 5' untranslated leaders of bacterial mRNAs that directly sense the levels of specific metabolites with a structurally conserved aptamer domain to regulate expression of downstream genes. Riboswitches are most common in the genomes of low GC Gram-positive bacteria (for example, Bacillus subtilis contains examples of all known riboswitches), and some riboswitch classes seem to be restricted to this group.

resultsWe used comparative sequence analysis and structural probing to identify five RNA elements (serC, speF, suhB, ybhL, and metA) that reside in the intergenic regions of Agrobacterium tumefaciens and many other alpha-proteobacteria. One of these, the metA motif, is found upstream of methionine biosynthesis genes and binds S-adenosylmethionine (SAM). This natural aptamer most likely functions as a SAM riboswitch (SAM-II) with a consensus sequence and structure that is distinct from the class of SAM riboswitches (SAM-I) predominantly found in Gram-positive bacteria. The minimal functional SAM-II aptamer consists of fewer than 70 nucleotides, which form a single stem and a pseudoknot. Despite its simple architecture and lower affinity for SAM, the SAM-II aptamer strongly discriminates against related compounds.

conclusionSAM-II is the only metabolite-binding riboswitch class identified so far that is not found in Gram-positive bacteria, and its existence demonstrates that biological systems can use multiple RNA structures to sense a single chemical compound. The two SAM riboswitches might be 'RNA World' relics that were selectively retained in certain bacterial lineages or new motifs that have emerged since the divergence of the major bacterial groups.

Indexed as

AlphaproteobacteriaAptamers, NucleotideBase SequenceGenes, SwitchMolecular Sequence DataNucleic Acid ConformationProtein BindingRegulatory Sequences, Ribonucleic AcidRNA, BacterialS-AdenosylmethionineAptamers, NucleotideRegulatory Sequences, Ribonucleic AcidRNA, BacterialS-Adenosylmethionine

Identifiers

PMID16086852
PMCPMC1273637
OpenAlexW2120200447

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.