Evidence map›Paper›PMID 41676371›Full record

ArticleQuantitative biology (Beijing, China)2024

Functional predictability of universal gene circuits in diverse microbial hosts.

Chenrui Qin, Tong Xu, Xuejin Zhao, Yeqing Zong, Haoqian M Zhang, Chunbo Lou, Qi Ouyang, Long Qian

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2024. 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. Toward predictable universal genetic circuit design.Quantitative biology (Beijing, China) · 2024
    Article
  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

8 authors.

Chenrui QinPeking-Tsinghua Joint Center for Life Sciences Peking University Beijing China.
Tong XuPeking-Tsinghua Joint Center for Life Sciences Peking University Beijing China.
Xuejin ZhaoCAS Key Laboratory of Microbial Physiological and Metabolic Engineering Institute of Microbiology Chinese Academy of Sciences Beijing China.
Yeqing ZongBluepha Co., Ltd Beijing China.
Haoqian M ZhangBluepha Co., Ltd Beijing China.
Chunbo LouCenter for Cell and Gene Circuit Design CAS Key Laboratory of Quantitative Engineering Biology Guangdong Provincial Key Laboratory of Synthetic Genomics Shenzhen Key Laboratory of Synthetic Genomics Shenzhen Institute of Synthetic Biology Shenzhen Institutes of Advanced Technology Chinese Academy of Sciences Shenzhen China.
Qi OuyangCenter for Quantitative Biology Academy for Advanced Interdisciplinary Studies Peking University Beijing China.
Long QianCenter for Quantitative Biology Academy for Advanced Interdisciplinary Studies Peking University Beijing China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the principles of synthetic biology were initially established in model bacteria, microbial producers, extremophiles and gut microbes have now emerged as valuable prokaryotic chassis for biological engineering. Extending the host range in which designed circuits can function reliably and predictably presents a major challenge for the concept of synthetic biology to materialize. In this work, we systematically characterized the cross-species universality of two transcriptional regulatory modules-the T7 RNA polymerase activator module and the repressors module-in three non-model microbes. We found striking linear relationships in circuit activities among different organisms for both modules. Parametrized model fitting revealed host non-specific parameters defining the universality of both modules. Lastly, a genetic NOT gate and a band-pass filter circuit were constructed from these modules and tested in non-model organisms. Combined models employing host non-specific parameters were successful in quantitatively predicting circuit behaviors, underscoring the potential of universal biological parts and predictive modeling in synthetic bioengineering.

Indexed as

circuit predictabilityhost‐independent genetic circuitshost‐nonspecific parametersparts characterizationtranscriptional regulatory modules

Identifiers

PMID41676371
PMCPMC12806508

What OpenQuestion holds

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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.