Evidence map›Paper›PMID 23681549›Full record

ArticleMolecular biology reports2013

p∆TubHA4C, a new versatile vector for constitutive expression in Drosophila.

Yan Zhang, Stephanie Arcia, Barbara Perez, Pedro Fernandez-Funez, Diego E Rincon-Limas

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Article in Molecular biology reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

5 citing papers in PubMed.

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4 · The record

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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.

Yan ZhangDepartment of Neurology, McKnight Brain Institute, University of Florida, Gainesville, FL 32611, USA.
Stephanie Arcia
Barbara Perez
Pedro Fernandez-Funez
Diego E Rincon-Limas

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several vectors for gene expression are available in Drosophila, a hub for genetics and genomics innovation. However, the vectors for ubiquitous expression have a complex structure, including coding exons, that makes in-frame cloning of cDNAs very complicated. In this report we describe a new Drosophila expression vector (p∆TubHA4C) for ubiquitous expression of coding sequences under the control of a minimal 0.9 kb promoter of α1 tubulin (α1t). This plasmid was designed to include optimized multiple cloning sites (polylinker) to provide flexibility in cloning strategies. We also added the option of double labeling the expressed proteins with two C-terminal tags, the viral epitope hemagglutinin and a synthetic tetracysteine (4C) tag that binds small fluorescent compounds. This dual tag allows both in situ and biochemical detection of the desired protein. In particular, the new 4C tag technology combines easy fluorescent labeling with small arsenical compounds in live or fixed cells and tissues, while producing minimal alterations to the tagged protein due to its small size. To demonstrate the potent and ubiquitous expression under the control of the ∆Tub promoter, bacterial lacZ was expressed and monitored in cell culture and transgenic flies. We found that the modified 0.9 kb ΔTub promoter induced similar expression levels to the intact 2.6 kb α1t promoter, supporting the inclusion of all critical regulatory elements in the new and flexible ∆TubHA4C vector.

Indexed as

AnimalsAnimals, Genetically ModifiedBase SequenceDNA PrimersDrosophilaFluorescenceFluorescent Antibody TechniqueGalactosidesGene ExpressionGenetic VectorsHemagglutininsIndolesMolecular Sequence DataPlasmidsPromoter Regions, GeneticReal-Time Polymerase Chain Reaction5-bromo-4-chloro-3-indolyl beta-galactosideDNA PrimersGalactosidesHemagglutininsIndolesTubulin

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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.