Evidence map›Paper›PMID 41890105›Full record

ArticlebioRxiv : the preprint server for biology2026

Improved vector toolkit for genome writing in mammalian cells.

Kelly Barriball, Brianna Berrios, Camilla Coelho, Sudarshan Pinglay, Yu Zhao, Noor Chalhoub, Tiffany Tsou, John T Atwater, Jef D Boeke, Weimin Zhang and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

11 authors.

Kelly BarriballInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.
Brianna BerriosInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.
Camilla CoelhoInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.
Sudarshan PinglayInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.ORCID 0000-0002-8781-1476
Yu ZhaoInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.
Noor ChalhoubInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.ORCID 0000-0001-6545-4618
Tiffany TsouInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.
John T AtwaterInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.
Jef D BoekeInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.ORCID 0000-0001-5322-4946
Weimin ZhangInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.ORCID 0000-0002-8836-1438
Ran BroshInstitute for Systems Genetics, NYU Langone Health, New York, NY, USA.ORCID 0000-0001-9714-8623

Funding

Supplement for Center for Synthetic Regulatory Genomics: Building CACNA1C alleles associated with Neuropsychiatric DisordersRM1HG009491 · NHGRI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jef D BOEKE · 2018 to 2026
$20.9M
Genomically rewritten and tailored humanized mouse models for various organ disordersR24OD037800 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Jef D BOEKE, Shane Liddelow · 2025 to 2026
$1.7M
NHGRI NIH HHS RM1 HG009491NIH HHS R24 OD037800
6 · The paper itself

Abstract

Efficient genome writing in mammalian cells requires robust methods for integrating large DNA payloads. The previously described method mammalian Switching Antibiotic resistance markers Progressively for Integration (mSwAP-In) enables iterative, biallelic genome rewriting in mammalian stem cells with DNA payloads exceeding 100 kb. However, the lack of standardized vectors and certain technical constraints have limited its broader adoption. Here we present an improved plasmid toolkit designed to streamline the implementation of mSwAP-In. The toolkit includes two core vectors. pLP-TK (pCTC174) is a landing-pad plasmid compatible with Golden Gate assembly of genomic homology arms and supports both mSwAP-In and the recombinase-mediated cassette exchange method Big-IN. mSwAP-In MC2v2 (pKBA135) is a versatile Big DNA assembly and delivery vector that supports Gibson-based assembly and incorporates positive, negative, and fluorescent selection markers, as well as a backbone counterselection cassette to minimize unwanted plasmid integration. The vector architecture also enables propagation in yeast and bacterial hosts, inducible plasmid copy-number amplification in standard E. coli strains, and CRISPR/Cas9-mediated payload release through preinstalled guide RNA target sites. We further characterize the FCU1/5-FC counterselection system in mouse embryonic stem cells and define conditions that minimize its bystander toxicity. Finally, we provide a set of Cas9-gRNA expression plasmids optimized for common mSwAP-In applications. Together, these reagents constitute a standardized and experimentally validated toolkit that simplifies large-scale genome writing using mSwAP-In.

Identifiers

PMID41890105
PMCPMC13015416

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.