Evidence map›Paper›PMID 23560087›Full record

ArticlePloS one2013

Quantitative design of regulatory elements based on high-precision strength prediction using artificial neural network.

Hailin Meng, Jianfeng Wang, Zhiqiang Xiong, Feng Xu, Guoping Zhao, Yong Wang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Towards AI-designed genomes using a variational autoencoder.Proceedings. Biological sciences · 2024
    Article
  3. Article
  4. Review
  5. Article
  6. Synthetic Biology Meets Machine Learning.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  7. Review
  8. Article
  9. ProD: A Tool for Predictive Design of Tailored Promoters in Escherichia coli.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Synbiological systems for complex natural products biosynthesis.Synthetic and systems biotechnology · 2016
    Review
  17. Synthetic promoter design for new microbial chassis.Biochemical Society transactions · 2016
    Review
  18. Article
  19. Advances and computational tools towards predictable design in biological engineering.Computational and mathematical methods in medicine · 2014
    Review
  20. Review
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 2 institutions in 1 country.

Hailin MengKey Laboratory of Synthetic Biology, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Jianfeng Wang
Zhiqiang Xiong
Feng Xu
Guoping Zhao
Yong Wang
Center for Excellence in Molecular Plant Sciences · CNShanghai Institutes for Biological Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate and controllable regulatory elements such as promoters and ribosome binding sites (RBSs) are indispensable tools to quantitatively regulate gene expression for rational pathway engineering. Therefore, de novo designing regulatory elements is brought back to the forefront of synthetic biology research. Here we developed a quantitative design method for regulatory elements based on strength prediction using artificial neural network (ANN). One hundred mutated Trc promoter & RBS sequences, which were finely characterized with a strength distribution from 0 to 3.559 (relative to the strength of the original sequence which was defined as 1), were used for model training and test. A precise strength prediction model, NET90_19_576, was finally constructed with high regression correlation coefficients of 0.98 for both model training and test. Sixteen artificial elements were in silico designed using this model. All of them were proved to have good consistency between the measured strength and our desired strength. The functional reliability of the designed elements was validated in two different genetic contexts. The designed parts were successfully utilized to improve the expression of BmK1 peptide toxin and fine-tune deoxy-xylulose phosphate pathway in Escherichia coli. Our results demonstrate that the methodology based on ANN model can de novo and quantitatively design regulatory elements with desired strengths, which are of great importance for synthetic biology applications.

Indexed as

Gene Expression Regulation, BacterialModels, GeneticPromoter Regions, GeneticAnimalsComputer SimulationEscherichia coliGenetic EngineeringNeural Networks, ComputerRecombinant ProteinsReproducibility of ResultsScorpionsScorpion VenomsXylosedeoxyxylulose phosphateKBT toxin, Buthus martensiiRecombinant ProteinsScorpion VenomsXylose

Identifiers

PMID23560087
PMCPMC3613377
OpenAlexW1966532770

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.