Evidence map›Paper›PMID 41652449›Full record

ArticleBMC research notes2026

SSA-like and MMEJ-like recombination events in a transgenic construct with in-cis programmed self-eliminating components in different E. coli strains.

Christian E Ogaugwu, Zach N Adelman

Abstract read
In one paragraph

Article in BMC research notes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Christian E OgaugwuDepartment of Entomology, Texas A&M University, College Station, TX, USA. christian.ogaugwu@ag.tamu.edu.
Zach N AdelmanDepartment of Entomology, Texas A&M University, College Station, TX, USA.

Funding

National Institute of Allergies and Infectious Diseases, National Institutes of Health AI148787
6 · The paper itself

Abstract

objectiveDNA repair pathways have been leveraged for genetic engineering strategies, including self-eliminating transgenes in insects. In effort towards establishing a self-eliminating transgenic system that leaves desired cargoes like antibodies or anti-viral molecules in Aedes aegypti, steps were taken to generate a plasmid with direct repeats and other necessary transgenic components. Here, we present an account of series of recombination events in E. coli that were encountered during the building of a multi-component plasmid for achieving a cargo-leaving self-eliminating transgenic system in Ae. aegypti.

resultsStep-wise construction of the multi-component plasmid in Stellar™ E. coli competent cells achieved successful modifications of a parent plasmid from a previous study by removing some DNA fragments, incorporating direct repeats and incorporating fluorescent marker gene cassettes (3xP3-DsRed and 3xP3-BFP) in desired locations. However, recombination events resulting in precise and repeatable deletions of small and large DNA fragments were obtained following incorporation of a target site for the in-cis-located I-SceI homing endonuclease into the plasmid. These events were also observed using other E. coli strains like SURE and NEB

Indexed as

Escherichia coliGenetic EngineeringPlasmidsRecombination, GeneticTransgenesAedesAnimalsAnimals, Genetically ModifiedDNA recombinationMicrohomology-mediated end joiningSingle-strand annealing

Identifiers

PMID41652449
PMCPMC12973924

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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.