Evidence map›Paper›PMID 33293335›Full record

ArticleLife science alliance2021

ESI mutagenesis: a one-step method for introducing mutations into bacterial artificial chromosomes.

Arnaud Rondelet, Andrei Pozniakovsky, Devika Namboodiri, Richard Cardoso da Silva, Divya Singh, Marit Leuschner, Ina Poser, Andrea Ssykor, Julian Berlitz, Nadine Schmidt and 4 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

14 authors at 2 institutions in 1 country.

Arnaud RondeletMax Planck Institute of Molecular Physiology, Dortmund, Germany.
Andrei PozniakovskyMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Devika NamboodiriMax Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0001-9490-0525
Richard Cardoso da SilvaMax Planck Institute of Molecular Physiology, Dortmund, Germany.
Divya SinghMax Planck Institute of Molecular Physiology, Dortmund, Germany.
Marit LeuschnerMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Ina PoserMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Andrea SsykorMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Julian BerlitzMax Planck Institute of Molecular Physiology, Dortmund, Germany.
Nadine SchmidtMax Planck Institute of Molecular Physiology, Dortmund, Germany.
Lea RöhderMax Planck Institute of Molecular Physiology, Dortmund, Germany.
Gerben VaderMax Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0001-5729-0991
Anthony A HymanMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Alexander W BirdMax Planck Institute of Molecular Physiology, Dortmund, Germany alex.bird@mpi-dortmund.mpg.de.ORCID 0000-0002-1061-0799
Max Planck Institute of Molecular Physiology · DEMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

European Research Council 638197
6 · The paper itself

Abstract

Bacterial artificial chromosome (BAC)-based transgenes have emerged as a powerful tool for controlled and conditional interrogation of protein function in higher eukaryotes. Although homologous recombination-based recombineering methods have streamlined the efficient integration of protein tags onto BAC transgenes, generating precise point mutations has remained less efficient and time-consuming. Here, we present a simplified method for inserting point mutations into BAC transgenes requiring a single recombineering step followed by antibiotic selection. This technique, which we call exogenous/synthetic intronization (ESI) mutagenesis, relies on co-integration of a mutation of interest along with a selectable marker gene, the latter of which is harboured in an artificial intron adjacent to the mutation site. Cell lines generated from ESI-mutated BACs express the transgenes equivalently to the endogenous gene, and all cells efficiently splice out the synthetic intron. Thus, ESI mutagenesis provides a robust and effective single-step method with high precision and high efficiency for mutating BAC transgenes.

Indexed as

Chromosomes, Artificial, BacterialTransgenesCell LineExonsGenetic EngineeringHomologous RecombinationHumansIntronsMutagenesis, InsertionalPhenotypePoint Mutation

Identifiers

PMID33293335
PMCPMC7756954
OpenAlexW3113201870

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.