High-fidelity human chromosome transfer and elimination

The synthesis of human genomes and other gigabase-scale genomes will require new strategies. Here, we realized key steps in our pipeline for building synthetic human chromosomes. We established: (i) the facile transfer of human chromosomes from human cells to mouse embryonic stem cells (assembly cells), where they are haploid, are nonessential, and may be operated on; (ii) the transfer of these human chromosomes from monochromosomal hybrids back into human cells to generate defined, synthetic aneuploidies; and (iii) the elimination of the corresponding endogenous human chromosomes to regenerate diploid cells containing a transferred chromosome. All steps were performed in nontransformed cells without chromothripsis and generated minimal structural variants, insertions, deletions, or single-nucleotide variants.

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Publication Details

Journal
Science
Published
2025-12-04
DOI
https://doi.org/10.1126/science.adv9797
Citations
1
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
0.81
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High-fidelity human chromosome transfer and elimination

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1 citations
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High-fidelity human chromosome transfer and elimination

Julian E. Sale, Jakob Birnbaum, Pierre Murat, Kim C. Liu, Gianluca Petris, Linda van Bijsterveldt, Jason W. Chin, Simona Grazioli
article en
1 citations

Abstract

The synthesis of human genomes and other gigabase-scale genomes will require new strategies. Here, we realized key steps in our pipeline for building synthetic human chromosomes. We established: (i) the facile transfer of human chromosomes from human cells to mouse embryonic stem cells (assembly cells), where they are haploid, are nonessential, and may be operated on; (ii) the transfer of these human chromosomes from monochromosomal hybrids back into human cells to generate defined, synthetic aneuploidies; and (iii) the elimination of the corresponding endogenous human chromosomes to regenerate diploid cells containing a transferred chromosome. All steps were performed in nontransformed cells without chromothripsis and generated minimal structural variants, insertions, deletions, or single-nucleotide variants.

ScienceVol. 390(6777)
MRC Laboratory of Molecular Biology (GB), Wellcome Sanger Institute (GB), Medical Research Council (GB)
Openalex Percentile: Top 21%
Pluripotent Stem Cells Research
0.81
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