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Deciphering integration loci of CHO manufacturing cell lines using long read nanopore sequencing.

Authors :
Clappier, Christian
Böttner, Dennis
Heinzelmann, Daniel
Stadermann, Anna
Schulz, Patrick
Schmidt, Moritz
Lindner, Benjamin
Source :
New Biotechnology. Jul2023, Vol. 75, p31-39. 9p.
Publication Year :
2023

Abstract

Despite advances in genetic characterization of Chinese hamster ovary (CHO) cell lines regarding identification of integration sites using next generation sequencing, e.g. targeted locus amplification sequencing (TLA-seq), the concatemer structure of the integrated vectors remains elusive. Here, the entire integration locus of two CHO manufacturing cell lines was reconstructed combining CRISPR/Cas9 target enrichment, nanopore sequencing and the Canu de novo assembly pipeline. An IgG producing CHO cell line integrated 3 vector copies, which were near full-length and contained all relevant vector elements such as transgenes and their promoters on each of the vector copies. In contrast, a second CHO cell line producing a bivalent bispecific antibody integrated 7 highly fragmented vector copies in different orientations leading to head-to-head and tail-to-tail fusions. The size of the vector fragments ranged from 3.0 to 11.4 kbp each carrying 1–3 transgenes. The breakpoints of the genome-vector and vector-vector junctions were validated using Sanger sequencing and Southern blotting. A comparison to TLA-seq data confirmed the genomic breakpoints, but most of the breakpoints of the vector-vector fusions were missed by TLA-seq. For the first time, the complete transgene locus of CHO manufacturing cell lines could be deciphered. Strikingly, the application of the nanopore long-read sequencing technology led to novel insights into the complexity of genomic transgene integrations of CHO manufacturing cell lines generated via random integration. • Nanopore sequencing resolves complete concatemer structure of randomly integrated vectors. • Assembly of concatemer structure reveals highly fragmented and depleted genetic architecture. • Cas9-based enrichment leads to 37-fold increase of expression vector coverage. • Complete concatemer structure allows for a thorough interpretation of complex Southern blot data. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18716784
Volume :
75
Database :
Academic Search Index
Journal :
New Biotechnology
Publication Type :
Academic Journal
Accession number :
162919340
Full Text :
https://doi.org/10.1016/j.nbt.2023.03.003