Whole-genome sequences reveal zygotic composition in chimeric twins

Yoon, C. J.; Nam, C. H.; Kim, T.; Lee, J. S.; Yi, K.; Kim, R.; Koh, J.-Y.; Kim, J.; Won, H.; Oh, J.; Griffith, O. L.; Griffith, M.; Sung, J.; Kim, T. Y.; Choi, J. S.; Cho, D.; Ju, Y. S.

doi:10.1101/2023.12.03.568663

bioRxiv · 10.1101/2023.12.03.568663

Whole-genome sequences reveal zygotic composition in chimeric twins

Yoon, C. J.·Nam, C. H.·Kim, T.·Lee, J. S.·Yi, K.·Kim, R.·Koh, J.-Y.·Kim, J.·Won, H.·Oh, J.·Griffith, O. L.·Griffith, M.·Sung, J.·Kim, T. Y.·Choi, J. S.·Cho, D.·Ju, Y. S.

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Abstract

The monochorionic placenta in dizygotic twins allows in utero exchange of embryonic cells, resulting in chimerism in the twins. In practice, this chimerism is incidentally identified on mixed ABO blood types or in the presence of cells with a discordant sex chromosome. Here, we applied whole-genome sequencing to one triplet and one twin families to precisely understand their zygotic compositions, using millions of genomic variants as barcodes of zygotic origins. Peripheral blood showed asymmetrical contributions from two sister zygotes, where one of the zygotes was the major clone in both twins. Single-cell RNA sequencing of peripheral blood tissues further showed differential contributions from the two sister zygotes across blood cell types. In contrast, buccal tissues were pure in genetic composition, suggesting that in utero cellular exchanges were confined to the blood tissues. Our study illustrates the cellular history of twinning during human development, which is critical for managing the health of chimeric individuals in the era of genomic medicine.

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Yoon, C. J., Nam, C. H., Kim, T., Lee, J. S., Yi, K., Kim, R., Koh, J.-Y., Kim, J., Won, H., Oh, J., Griffith, O. L., Griffith, M., Sung, J., Kim, T. Y., Choi, J. S., Cho, D., Ju, Y. S.. 2023-12-05. Whole-genome sequences reveal zygotic composition in chimeric twins. https://doi.org/10.1101/2023.12.03.568663

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