bioRxivGeneticsPreprint
Cytosine base editing workflow for quality-controlled multiplex-knockout hiPSC lines
Vanessa KirschneriD, Julia Herzberg, Christin Richter, Sayari Bhunia, Rebecca Kistler, Roger OttenheijmiD, Timon SeegeriD, Marc FreicheliD, Alex CorneaniD
Abstract
Dissecting polygenic disease mechanisms requires human cell models that harbour multiple targeted genetic modifications in a defined background. However, generating and rigorously validating such models remains difficult. We developed a cytosine base editing workflow to generate multiplex-knockout (KO) human induced pluripotent stem cell (hiPSC) lines. First, we assessed six cytosine base editor (CBE) variants and selected evoBE4max. We then combined sgRNA-guided introduction of premature termination codons and splice-site mutations with fluorescence-based enrichment. This yielded a median on-target C-to-T editing efficiency of 77.5% (range, 27.0-86.5%) across six loci. We generated single-, double-, and triple-KO hiPSC lines for endolysosomal Ca{superscript 2} signalling components (OCaR2, TPC1, TPC2) and confirmed loss-of-function at transcript and protein levels. We performed extensive quality control, including pluripotency assessment, SNP-array karyotyping, and whole-genome sequencing, which indicated minimal guide-directed off-target editing. We further extended multiplex editing to ORAI Ca{superscript 2} channel paralogs. This framework supports scalable production of quality-controlled multiplex-KO hiPSC lines.
- organism: human
- assay: whole-genome sequencing
- research focus: variant calling
- approach: experimental assay
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Direct delivery of stabilized Cas-embedded base editors achieves efficient and accurate editing of clinically relevant targets
J. M. Lee, J. Zeng, … C. A. Schiffer·bioRxiv·Feb 8, 2024
- Minimal activation of the p53 DNA damage response by a modular cytosine base editor enables effective multiplexed gene knockout in induced pluripotent stem cells
Robert A. Blassberg, Olga Mielczarek, … Immacolata Porreca·bioRxiv·Jun 5, 2025
- Precision genome-editing with CRISPR/Cas9 in human induced pluripotent stem cells
John Budde, Rita J. Martinez, … Celeste M M. Karch·bioRxiv·Sep 12, 2017
- Near-perfect precise on-target editing of human hematopoietic stem and progenitor cells
F.-M. Cloarec-Ung, J. Beaulieu, … D. J. Knapp·bioRxiv·May 26, 2023
- Selection-free, high frequency genome editing by homologous recombination of human pluripotent stem cells using Cas9 RNP and AAV6
Renata M. Martin, Kazuya Ikeda, … Matthew Porteus·bioRxiv·Jan 23, 2018
- Efficient installation of heterozygous mutations in human pluripotent stem cells using prime editing
Annabelle Suter, Alison N. Graham, … Sara E. Howden·The CRISPR JournalPeer-reviewed·Sep 24, 2025