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Updated: Dec 4, 2025

Deciphering High-Resolution 3D Chromatin Organization via Capture Hi-C
Published on: October 14, 2022
High-resolution three-dimensional chromatin profiling of the Chinese hamster ovary cell genome
Stephen Bevan1,2, Stefan Schoenfelder1,2, Robert J Young3
1Nuclear Dynamics Programme, The Babraham Institute, Babraham Research Campus, Cambridge, UK.
Abstract:
Chinese hamster ovary (CHO) cell lines are the pillars of a multibillion-dollar biopharmaceutical industry producing recombinant therapeutic proteins. The effects of local chromatin organization and epigenetic repression within these cell lines result in unpredictable and unstable transgene expression following random integration. Limited knowledge of the CHO genome and its higher order chromatin organization has thus far impeded functional genomics approaches required to tackle these issues. Here, we present an integrative three-dimensional (3D) map of genome organization within the CHOK1SV® 10E9 cell line in conjunction with an improved, less fragmented CHOK1SV 10E9 genome assembly. Using our high-resolution chromatin conformation datasets, we have assigned ≈90% of sequence to a chromosome-scale genome assembly. Our genome-wide 3D map identifies higher order chromatin structures such as topologically associated domains, incorporates our chromatin accessibility data to enhance the identification of active cis-regulatory elements, and importantly links these cis-regulatory elements to target promoters in a 3D promoter interactome. We demonstrate the power of our improved functional annotation by evaluating the 3D landscape of a transgene integration site and two phenotypically different cell lines. Our work opens up further novel genome engineering targets, has the potential to inform vital improvements for industrial biotherapeutic production, and represents a significant advancement for CHO cell line development.
Insights
Researchers mapped the 3D genome organization in Chinese hamster ovary (CHO) cells, improving genome assembly and identifying regulatory elements. This advances biotherapeutic production by enabling better CHO cell line development.
Area of Science:
- Genomics
- Cell Biology
- Biotechnology
Background:
- Chinese hamster ovary (CHO) cells are crucial for biopharmaceutical production of recombinant proteins.
- Unpredictable transgene expression in CHO cells stems from poor understanding of genome organization and epigenetic repression.
- Limited knowledge of CHO genome structure hinders functional genomics and cell line improvement.
Purpose of the Study:
- To create an integrated 3D genome organization map for the CHOK1SV® 10E9 cell line.
- To improve the CHOK1SV® 10E9 genome assembly.
- To identify cis-regulatory elements and their interactions with promoters in 3D space.
Main Methods:
- High-resolution chromatin conformation capture (Hi-C) datasets were generated.
- An improved, chromosome-scale genome assembly was created for CHOK1SV® 10E9 cells.
- Chromatin accessibility data was integrated with 3D genome organization data.
Main Results:
- An integrative 3D genome map was generated, assigning ~90% of sequences to chromosome-scale assembly.
- The map identified topologically associated domains and active cis-regulatory elements.
- A 3D promoter interactome linked cis-regulatory elements to target promoters, demonstrating utility in analyzing transgene integration sites.
Conclusions:
- The improved genome assembly and 3D map provide a foundation for functional genomics in CHO cells.
- This work identifies novel targets for genome engineering to enhance biotherapeutic production.
- The findings represent a significant advancement for CHO cell line development and industrial biomanufacturing.
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