Computationally defined and in vitro validated putative genomic safe harbour loci for transgene expression in human cells

Author:

Autio Matias I123ORCID,Motakis Efthymios2,Perrin Arnaud12ORCID,Bin Amin Talal3,Tiang Zenia12,Do Dang Vinh12,Wang Jiaxu4,Tan Joanna5,Ding Shirley Suet Lee6,Tan Wei Xuan67,Lee Chang Jie Mick12,Teo Adrian Kee Keong678ORCID,Foo Roger SY12

Affiliation:

1. Laboratory of Molecular Epigenomics and Chromatin Organization, Genome Institute of Singapore

2. Cardiovascular Disease Translational Research Programme, Yong Loo Lin School of Medicine

3. Laboratory of Systems Biology and Data Analytics, Genome Institute of Singapore

4. Laboratory of RNA Genomics and Structure, Genome Institute of Singapore

5. Center for Genome Diagnostics, Genome Institute of Singapore

6. Stem Cells and Diabetes Laboratory, Institute of Molecular and Cell Biology

7. Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore

8. Precision Medicine Translational Research Programme, Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore

Abstract

Selection of the target site is an inherent question for any project aiming for directed transgene integration. Genomic safe harbour (GSH) loci have been proposed as safe sites in the human genome for transgene integration. Although several sites have been characterised for transgene integration in the literature, most of these do not meet criteria set out for a GSH and the limited set that do have not been characterised extensively. Here, we conducted a computational analysis using publicly available data to identify 25 unique putative GSH loci that reside in active chromosomal compartments. We validated stable transgene expression and minimal disruption of the native transcriptome in three GSH sites in vitro using human embryonic stem cells (hESCs) and their differentiated progeny. Furthermore, for easy targeted transgene expression, we have engineered constitutive landing pad expression constructs into the three validated GSH in hESCs.

Funder

Biomedical Research Council

Agency for Science, Technology and Research

Publisher

eLife Sciences Publications, Ltd

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