Gambogi Craig W, Mer Elie, Brown David M, Yankson George, Gavade Janardan N, Logsdon Glennis A, Heun Patrick, Glass John I, Black Ben E
Department of Biochemistry and Biophysics.
Graduate Program in Biochemistry and Molecular Biophysics.
bioRxiv. 2023 Jun 30:2023.06.30.547284. doi: 10.1101/2023.06.30.547284.
Large DNA assembly methodologies underlie milestone achievements in synthetic prokaryotic and budding yeast chromosomes. While budding yeast control chromosome inheritance through ~125 bp DNA sequence-defined centromeres, mammals and many other eukaryotes use large, epigenetic centromeres. Harnessing centromere epigenetics permits human artificial chromosome (HAC) formation but is not sufficient to avoid rampant multimerization of the initial DNA molecule upon introduction to cells. Here, we describe an approach that efficiently forms single-copy HACs. It employs a ~750 kb construct that is sufficiently large to house the distinct chromatin types present at the inner and outer centromere, obviating the need to multimerize. Delivery to mammalian cells is streamlined by employing yeast spheroplast fusion. These developments permit faithful chromosome engineering in the context of metazoan cells.
