Evidence map›Paper›PMID 16757798›Full record

ArticleMolecular biotechnology2006

Reporter system for the detection of in vivo gene conversion: changing colors from blue to green using GFP variants.

Jeffrey R Sommer, Jon Alderson, Goetz Laible, Robert M Petters

Abstract read
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In one paragraph

Article in Molecular biotechnology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Reporter genes and transgenicFrontiers in medicine · 2025
    Review
  2. 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

4 authors.

Jeffrey R SommerDepartment of Animal Science, North Carolina State University, Raleigh, NC 27695, USA.
Jon Alderson
Goetz Laible
Robert M Petters

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have devised a system for the study of in vivo gene correction based on the detection of color variants of the green fluorescent protein (GFP) from the jellyfish Aequorea victoria. The intensity and spectra of the fluorescence emitted by the blue (BFP) and red-shifted (EGFP) variants of GFP differ from each other. We modified one nucleotide from an EGFP expression vector that we predicted would yield a blue variant (TAC-CAC, Tyr(66)-His(66)). Cells that were either transiently or stably transfected with the reporter system were used to test the functionality and feasibility of the detection of in vivo gene correction. A thio-protected single-stranded oligonucleotide designed to convert the genotype of the blue variant to that of the EGFP variant by the correction of a single base pair was delivered to the reporter cells using a variety of methodologies and strategies.Conversion events were easily observed using fluorescent microscopy because of the enhanced emission intensity and different spectra of the EGFP variant.

Indexed as

Genes, ReporterGenetic TechniquesAmino Acid SequenceAnimalsBase SequenceCHO CellsClone CellsColorCricetinaeCricetulusGene ConversionGreen Fluorescent ProteinsLuminescent ProteinsMolecular Sequence DataMutationOligonucleotidesblue fluorescent protein, Aequorea victoriaGreen Fluorescent ProteinsLuminescent ProteinsOligonucleotides

Identifiers

PMID16757798

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.