Evidence map›Paper›PMID 24376833›Full record

ArticlePloS one2013

Functional characterization of the origin of replication of pRN1 from Sulfolobus islandicus REN1H1.

Chijioke J Joshua, Luis D Perez, Jay D Keasling

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
0.7field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Archaeal extrachromosomal genetic elements.Microbiology and molecular biology reviews : MMBR · 2015
    Review
  2. Review
  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

3 authors at 2 institutions in 1 country.

Chijioke J JoshuaDepartment of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, United States of America ; Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America ; Joint BioEnergy Institute, Emeryville, California, United States of America.
Luis D PerezDepartment of Molecular and Cell Biology, University of California, Berkeley, Berkeley, California, United States of America ; Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America ; Joint BioEnergy Institute, Emeryville, California, United States of America.
Jay D KeaslingDepartment of Plant and Microbial Biology, University of California, Berkeley, Berkeley, California, United States of America ; Department of Chemical & Biomolecular Engineering, University of California, Berkeley, Berkeley, California, United States of America ; Physical Biosciences Division, Lawrence Berkeley National Laboratory, Berkeley, California, United States of America ; Joint BioEnergy Institute, Emeryville, California, United States of America ; Department of Bioengineering, University of California, Berkeley, Berkeley, California, United States of America.
Joint BioEnergy Institute · USUniversity of California, Berkeley · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmid pRN1 from Sulfolobus islandicus REN1H1 is believed to replicate by a rolling circle mechanism but its origin and mechanism of replication are not well understood. We sought to create minimal expression vectors based on pRN1 that would be useful for heterologous gene expression in S. acidocaldarius, and in the process improve our understanding of the mechanism of replication. We constructed and transformed shuttle vectors that harbored different contiguous stretches of DNA from pRN1 into S. acidocaldarius E4-39, a uracil auxotroph. A 232-bp region 3' of orf904 was found to be critical for pRN1 replication and is therefore proposed to be the putative origin of replication. This 232-bp region contains a 100-bp stem-loop structure believed to be the double-strand origin of replication. The loop of the 100-bp structure contains a GTG tri-nucleotide motif, a feature that was previously reported to be important for the primase activity of Orf904. This putative origin and the associated orf56 and orf904 were identified as the minimal replicon of pRN1 because transformants of plasmids lacking any of these three features were not recovered. Plasmids lacking orf904 and orf56 but harboring the putative origin were transformable when orf904 and orf56 were provided in-trans; a 75-bp region 5' of the orf904 start codon was found to be essential for this complementation. Detailed knowledge of the pRN1 origin of replication will broaden the application of the plasmid as a genetic tool for Sulfolobus species.

Indexed as

AnimalsBase SequenceDNA ReplicationGenetic VectorsMolecular Sequence DataPlasmidsReplication OriginSulfolobus

Identifiers

PMID24376833
PMCPMC3869888
OpenAlexW2032119670

What OpenQuestion holds

Textmetadata
LicenceCC0
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.