Evidence map›Paper›PMID 42420731›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Intercellular CRISPRi for Distributed Genetic Circuits.

Abhinav Pujar, Anchita Sharma, Manish Kushwaha

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Abhinav PujarUniversité Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Anchita SharmaUniversité Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France.
Manish KushwahaUniversité Paris-Saclay, INRAE, AgroParisTech, Micalis Institute, Jouy-en-Josas, France. manish.kushwaha@inrae.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbial communities and multicellular organisms employ diverse strategies for allocation of available resources, achieved through task distribution among specialized cells. Drawing inspiration from nature, several synthetic multicellular circuits have been recently constructed where a larger circuit is distributed into several cells in order to reduce the burden on individual cells. Here, we describe the implementation of multicellular logic-gate circuits in bacterial co-cultures that combine DNA messaging with CRISPRi regulation. Leveraging the easily programmable and information-dense DNA molecules, our system is composed of sender bacteria that transmit DNA messages encoding guide RNAs and receiver bacteria that receive them and express the guide RNAs to regulate transcription by CRISPR interference. We demonstrate several functional multicellular circuits representing digital logic gates that operate on timescales comparable to small molecule signaling: NOT, YES, AND, and AND-AND-NOT. The receiver cells process the inputs received to perform computations and generate a logical output.

Indexed as

Clustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsGene Regulatory NetworksBacteriaEscherichia coliRNA, Guide, CRISPR-Cas SystemsSynthetic BiologyRNA, Guide, CRISPR-Cas SystemsCombinational logicCRISPR interferenceDistributed computationM13 bacteriophageMulticellular circuits

Identifiers

PMID42420731

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.