Evidence map›Paper›PMID 24215641›Full record

ArticleBioTechniques2013

New vectors for epitope tagging and gene disruption in Schizosaccharomyces pombe.

Mariana C Gadaleta, Osamu Iwasaki, Chiaki Noguchi, Ken-ichi Noma, Eishi Noguchi

Abstract read
In one paragraph

Article in BioTechniques, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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  15. Chromatin immunoprecipitation to detect DNA replication and repair factors.Methods in molecular biology (Clifton, N.J.) · 2015
    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

5 authors.

Mariana C GadaletaDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA.
Osamu Iwasaki
Chiaki Noguchi
Ken-ichi Noma
Eishi Noguchi

Funding

A New Methodology to Decipher Three-Dimensional Genome StructureDP2OD004348 · OD · WISTAR INSTITUTE · PI NOMA, KENICHI · 2008 to 2008
$3.1M
Studies of the Swi1-Swi3 Replication Fork Protection ComplexR01GM077604 · NIGMS · DREXEL UNIVERSITY · PI NOGUCHI, EISHI · 2008 to 2012
$1.6M
NIGMS NIH HHS R01 GM077604NIGMS NIH HHS R01GM077604NIH HHS DP2 OD004348NIH HHS DP2-OD004348
6 · The paper itself

Abstract

We describe a series of new vectors for PCR-based epitope tagging and gene disruption in the fission yeast Schizosaccharomyces pombe, an exceptional model organism for the study of cellular processes. The vectors are designed for amplification of gene-targeting DNA cassettes and integration into specific genetic loci, allowing expression of proteins fused to 12 tandem copies of the Pk (V5) epitope or 5 tandem copies of the FLAG epitope with a glycine linker. These vectors are available with various antibiotic or nutritional markers and are useful for protein studies using biochemical and cell biological methods. We also describe new vectors for fluorescent protein-tagging and gene disruption using ura4MX6, LEU2MX6, and his3MX6 selection markers, allowing researchers in the S. pombe community to disrupt genes and manipulate genomic loci using primer sets already available for the widely used pFA6a-MX6 system. Our new vectors may also be useful for gene manipulation in Saccharomyces cerevisiae.

Indexed as

DNA, FungalEpitopesGene DeletionGene TargetingGenetic VectorsPolymerase Chain ReactionSchizosaccharomycesDNA, FungalEpitopes

Identifiers

PMID24215641
PMCPMC3880554

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Registered trials

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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.