Evidence map›Paper›PMID 24413461›Full record

ArticleNature chemical biology2014

Designable DNA-binding domains enable construction of logic circuits in mammalian cells.

Rok Gaber, Tina Lebar, Andreja Majerle, Branko Šter, Andrej Dobnikar, Mojca Benčina, Roman Jerala

Abstract read
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In one paragraph

Article in Nature chemical biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

54 citing papers in PubMed, 108 citations in OpenAlex.

  1. Review
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  8. Engineering signalling pathways in mammalian cells.Nature biomedical engineering · 2024
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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

7 authors at 2 institutions in 1 country.

Rok Gaber1] Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia. [2] EN-FIST Centre of Excellence, Ljubljana, Slovenia. [3].
Tina Lebar1] Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia. [2] EN-FIST Centre of Excellence, Ljubljana, Slovenia. [3].
Andreja Majerle1] Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia. [2] EN-FIST Centre of Excellence, Ljubljana, Slovenia.
Branko ŠterFaculty of Computer and Information Science, University of Ljubljana, Slovenia.
Andrej DobnikarFaculty of Computer and Information Science, University of Ljubljana, Slovenia.
Mojca Benčina1] Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia. [2] EN-FIST Centre of Excellence, Ljubljana, Slovenia.
Roman Jerala1] Department of Biotechnology, National Institute of Chemistry, Ljubljana, Slovenia. [2] EN-FIST Centre of Excellence, Ljubljana, Slovenia.ORCID 0000000263375251
EN-FIST Centre of Excellence (Slovenia) · SIUniversity of Ljubljana · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Electronic computer circuits consisting of a large number of connected logic gates of the same type, such as NOR, can be easily fabricated and can implement any logic function. In contrast, designed genetic circuits must employ orthogonal information mediators owing to free diffusion within the cell. Combinatorial diversity and orthogonality can be provided by designable DNA- binding domains. Here, we employed the transcription activator-like repressors to optimize the construction of orthogonal functionally complete NOR gates to construct logic circuits. We used transient transfection to implement all 16 two-input logic functions from combinations of the same type of NOR gates within mammalian cells. Additionally, we present a genetic logic circuit where one input is used to select between an AND and OR function to process the data input using the same circuit. This demonstrates the potential of designable modular transcription factors for the construction of complex biological information-processing devices.

Indexed as

Amino Acid MotifsSynthetic BiologyAnimalsBinding SitesDNAFlow CytometryHEK293 CellsHumansLogicProtein Structure, TertiaryDNA

Identifiers

PMID24413461
OpenAlexW2062573403

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.