Evidence map›Paper›PMID 35864445›Full record

ArticleBMC plant biology2022

Development of dual reporter vector system for estimating translational activity of regulatory elements.

Aleksandra V Suhorukova, Alexander A Tyurin, Olga S Pavlenko, Orkhan N Mustafayev, Igor G Sinelnikov, Irina V Goldenkova-Pavlova

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

6 authors at 3 institutions in 2 countries.

Aleksandra V SuhorukovaLaboratory of functional genomics, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Moscow, Russia.
Alexander A TyurinLaboratory of functional genomics, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Moscow, Russia. alexjofar@gmail.com.
Olga S PavlenkoLaboratory of functional genomics, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Moscow, Russia.
Orkhan N MustafayevGenetic resources institute, Azerbaijan National Academy of Sciences, Baku, Azerbaijan.
Igor G SinelnikovLaboratory of enzyme biotechnology, Federal Research Centre "Fundamentals of Biotechnology", Russian Academy of Sciences, Moscow, Russia.
Irina V Goldenkova-PavlovaLaboratory of functional genomics, Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, Moscow, Russia.
Timiryazev Institute of Plant Physiology · RUAzerbaijan National Academy of Sciences · AZFederal Center Research Fundamentals of Biotechnology · RU

Funding

Ministry of Science and Higher Education of the Russian Federation 121033000137-1Russian Science Foundation RSF 22-14-00057
6 · The paper itself

Abstract

backgroundFor the needs of modern biotechnology, a quantitative approach to the control of regulatory elements at all stages of gene expression has long become indispensable. Such a control regime is impossible without a quantitative analysis of the role of each regulatory element or pattern used. Therefore, it seems important to modify and develop the accuracy, reproducibility, and availability of methods for quantifying the contribution of each regulatory code to the implementation of genetic information.

resultsA new vector system for transient expression in plants is described; this system is intended for quantitative analysis of the contribution of regulatory elements to transcription and translation efficiencies. The proposed vector comprises two expression cassettes carrying reporter genes (of the Clostridium thermocellum thermostable lichenase and E. coli β-glucuronidase) under the control of different promoters. Herewith we also propose a new method for quantification of the effect of tested regulatory elements on expression, which relies on assessment of the enzyme activities of reporter proteins taking into account the transcription of their genes.

conclusionsIn our view, this approach makes it possible to precisely determine the amounts of reporter proteins and their transcripts at all stages of expression. The efficiency of the proposed system has been validated by the analysis of the roles of known translation enhancers at the stages of transcription and translation.

Indexed as

Escherichia coliRegulatory Sequences, Nucleic AcidGenes, ReporterPromoter Regions, GeneticReproducibility of ResultsHigh throughput screeningLichenaseRegulatory elementsTransient expressionVectorβ-glucuronidase

Identifiers

PMID35864445
PMCPMC9306140
OpenAlexW4286493972

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.