Evidence map›Paper›PMID 22865840›Full record

ArticleJournal of bacteriology2012

Origin and fate of the 3' ends of single-stranded DNA generated by conjugal transfer of plasmid R1162.

Eric C Becker, Richard Meyer

Abstract read
In one paragraph

Article in Journal of bacteriology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

2 authors.

Eric C BeckerSection of Molecular Genetics and Microbiology, School of Biology and Institute of Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas, USA.
Richard Meyer

Funding

CONJUGATIVE MOBILIZATION OF PLASMID R1162R01GM037462 · NIGMS · UNIVERSITY OF TEXAS AUSTIN · PI MEYER, RICHARD J · 1987 to 2003
$997k
NIGMS NIH HHS GM37462NIGMS NIH HHS R01 GM037462
6 · The paper itself

Abstract

During conjugation, a single strand of DNA is cleaved at the origin of transfer (oriT) by the plasmid-encoded relaxase. This strand is then unwound from its complement and transferred in the 5'-to-3' direction, with the 3' end likely extended by rolling-circle replication. The resulting, newly synthesized oriT must then be cleaved as well, prior to recircularization of the strand in the recipient. Evidence is presented here that the R1162 relaxase contains only a single nucleophile capable of cleaving at oriT, with another molecule therefore required to cleave at a second site. An assay functionally isolating this second cleavage shows that this reaction can take place in the donor cell. As a result, there is a flux of strands with free 3' ends into the recipient. These ends are susceptible to degradation by exonuclease I. The degree of susceptibility is affected by the presence of an uncleaved oriT within the strand. A model is presented where these internal oriTs bind and trap the relaxase molecule covalently bound to the 5' end of the incoming strand. Such a mechanism would result in the preferential degradation of transferred DNA that had not been properly cleaved in the donor.

Indexed as

Base SequenceCatalytic DomainConjugation, GeneticDNA, BacterialElectrophoresis, Gel, Two-DimensionalEscherichia coli K12Escherichia coli ProteinsExodeoxyribonucleasesGene Expression Regulation, BacterialPlasmidsProtein BindingDNA, BacterialEscherichia coli Proteinsexodeoxyribonuclease IExodeoxyribonucleasesmobA protein, E coli

Identifiers

PMID22865840
PMCPMC3457208

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.