Evidence map›Paper›PMID 12533482›Full record

ArticleJournal of bacteriology2003

Traffic at the tmRNA gene.

Kelly P Williams

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bacteriology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Comparative genomics revealsApplied and environmental microbiology · 2026
    Article
  2. Exploring Mobile Genetic Elements in Vibrio cholerae.Genome biology and evolution · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Improved Mobilome Delineation in Fragmented Genomes.Frontiers in bioinformatics · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Ecological genomics of marine picocyanobacteria.Microbiology and molecular biology reviews : MMBR · 2009
    Review
  20. Article
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

1 author at 1 institution in 1 country.

Kelly P WilliamsDepartment of Biology, Indiana University, 1001 E. Third Street, Bloomington, IN 47405, USA. kellwill@indiana.edu
Indiana University Bloomington · US

Funding

TMRNA AND TRANS TRANSLATION--MECHANISM AND BIOLOGYR01GM059881 · NIGMS · INDIANA UNIVERSITY BLOOMINGTON · PI WILLIAMS, KELLY P. · 1999 to 2003
$1.0M
NIGMS NIH HHS GM 59881NIGMS NIH HHS R01 GM059881
6 · The paper itself

Abstract

A partial screen for genetic elements integrated into completely sequenced bacterial genomes shows more significant bias in specificity for the tmRNA gene (ssrA) than for any type of tRNA gene. Horizontal gene transfer, a major avenue of bacterial evolution, was assessed by focusing on elements using this single attachment locus. Diverse elements use ssrA; among enterobacteria alone, at least four different integrase subfamilies have independently evolved specificity for ssrA, and almost every strain analyzed presents a unique set of integrated elements. Even elements using essentially the same integrase can be very diverse, as is a group with an ssrA-specific integrase of the P4 subfamily. This same integrase appears to promote damage routinely at attachment sites, which may be adaptive. Elements in arrays can recombine; one such event mediated by invertible DNA segments within neighboring elements likely explains the monophasic nature of Salmonella enterica serovar Typhi. One of a limited set of conserved sequences occurs at the attachment site of each enterobacterial element, apparently serving as a transcriptional terminator for ssrA. Elements were usually found integrated into tRNA-like sequence at the 3' end of ssrA, at subsites corresponding to those used in tRNA genes; an exception was found at the non-tRNA-like 3' end produced by ssrA gene permutation in cyanobacteria, suggesting that, during the evolution of new site specificity by integrases, tropism toward a conserved 3' end of an RNA gene may be as strong as toward a tRNA-like sequence. The proximity of ssrA and smpB, which act in concert, was also surveyed.

Indexed as

Attachment Sites, MicrobiologicalBacterial ProteinsBase SequenceConserved SequenceIntegrasesMembrane ProteinsMolecular Sequence DataPhylogenyRNA, BacterialRNA, TransferSalmonellaAttR protein, bacteriaBacterial ProteinsIntegrasesMembrane ProteinsRNA, BacterialRNA, TransfersmpB protein, Staphylococcus hoministmRNA

Identifiers

PMID12533482
PMCPMC142792
OpenAlexW2155488611

What OpenQuestion holds

Textmetadata
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.