Authors
Luquette, L. J., Coorens, T. H. H., Natu, A., Suvakov, M., Caplin, A., Jun, M. S., Mo, A., Pelt, J., Anderson, L., Berselli, M., Bhamidipati, S., Blanchard, T., Brew, J., Chun, H.-J. E., Chun, H., Dehankar, M. K., Feng, W. C., Furatero, R., Grochowski, C. M., Ho, E., Jang, Y., Kottapalli, K., Leonard, M. K., Lim, N. S., Lindsay, T., Nicholson, S., Raimondi, I., Runnels, A., Scharlee, C., Shin, J., Veit, A. D., VonDran, M., Wang, Y., Yuan, D. J., Zhao, Y., Bell, T. J., Ardlie, K., Doddapaneni, H., Fulton, R., Germer, S., Landau, D., Oh, J. W., Park, P. J., Vaccarino, F. M., Walsh, C. A., Abyzov
Abstract
Single-cell DNA sequencing offers a powerful means of studying somatic mosaicism but requires careful analysis to mitigate DNA amplification-related artifacts. We performed primary template-directed amplification (PTA) and sequencing of 102 nuclei from postmortem lung and colon tissues of a 74-year-old male. Single-cell mutation burdens and spectra were validated by duplex sequencing and revealed heterogeneity across organs and cells, including signatures of APOBEC activity and tobacco exposure. Cells from both tissues exhibited chromosomal aneuploidies, loss of chromosome Y, and chromosomal rearrangements including rearrangements of the T-cell receptor loci indicative of T-cells. Shared embryonic mutations between cells enabled reconstruction of cellular ancestries from the zygote, which were validated by bulk sequencing. Collectively, we demonstrate a comprehensive approach for single-cell genomics that yields an expansive view of diverse somatic mutation types from development through aging across diverse tissues--insights that are obscured in bulk sequencing and only partially captured by other single-cell methods.
Preprint server:
bioRxiv
The authors list and abstract were imported from bioRxiv on 04 Nov 2025.
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