DNA methylation meets lineage tracing: History, recent progress, and future directions

Abstract

Lineage tracing techniques have been developed rapidly in the past decades by employing new genetic engineering tools. However, due to their invasive nature, these are difficult to apply to humans. Although endogenous DNA mutations can be used for in vivo lineage tracing in humans, their extremely low mutation rate presents substantial technical challenges. Epimutations on DNA methylation happen at a rate of about 0.001 per CpG site per division. Such rich and stable information enables high-resolution, noninvasive lineage tracing in humans, as recently achieved with both MethylTree and EPI-Clone. MethylTree is a computational innovation that accurately predicts cell lineages from single-cell DNA methylation data, be it genome-wide or targeted. EPI-Clone is a targeted approach that requires careful CpG panel selection for specific tissues, which has been validated in blood. In this review, we present an overview of related historical studies, discuss the development of both MethylTree and EPI-Clone, and compare these two approaches. Although EPI-Clone is more scalable and cheaper, MethylTree has a higher resolution and works directly across different tissues. We demonstrate here that MethylTree also works well with EPI-Clone data, thus providing a unified solution for epimutation-based lineage tracing. Finally, we highlight the advantages of epimutation-based lineage tracing, discuss future directions for tool development, and touch on considerations in biological applications. Epimutation-based lineage tracing opens up an exciting avenue for noninvasive lineage tracing in humans across many biological processes.

Keywords

DNA methylation / lineage tracing / single-cell multi-omics

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The Author(s). Quantitative Biology published by John Wiley & Sons Australia, Ltd on behalf of Higher Education Press.