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Somatic mosaicism rewires transcriptional and epigenetic states in clonal hematopoiesis

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Multi-modal single-cell sequencing enables mapping of mutant and wild-type human hematopoietic stem and progenitor cells within the same person, to define cellular phenotypic and epigenetic perturbations associated with clonal hematopoiesis.

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Fig. 1: Single-cell multi-omics analyses of CH.

References

  1. Mustjoki, S. & Young, N. S. Somatic mutations in ‘benign’ disease. N. Engl. J. Med. 384, 2039–2052 (2021). This review article presents the current understanding of somatic mosaicism and its effects on human disease.

    Article  CAS  Google Scholar 

  2. Jaiswal, S. et al. Age-related clonal hematopoiesis associated with adverse outcomes. N. Engl. J. Med. 371, 2488–2498 (2014). This paper reports the high prevalence of CH and the associated increased risk of developing hematopoietic malignancies.

    Article  Google Scholar 

  3. Nam, A. S. et al. Somatic mutations and cell identity linked by genotyping of transcriptomes. Nature 571, 355–360 (2019). This article reports the development of single-cell multi-omics that capture the mutational status and whole transcriptomes of hematopoietic stem progenitor cells.

    Article  CAS  Google Scholar 

  4. Gaiti, F. et al. Epigenetic evolution and lineage histories of chronic lymphocytic leukaemia. Nature 569, 576–580 (2019). This paper presents multi-modality single-cell sequencing that enables single-cell lineage tracing, linked with transcriptional and mutational status.

    Article  CAS  Google Scholar 

  5. Nam, A. S. et al. Integrating genetic and non-genetic determinants of cancer evolution by single-cell multi-omics. Nat. Rev. Genet. 22, 3–18 (2021). This review article presents the role of single-cell multi-omics in delineating the clonal evolution of human cancer by integrating genetic, cell state, epigenetic, and micro-environmental factors that enable fitness.

    Article  CAS  Google Scholar 

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This is a summary of: Nam, A. S. et al. Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation. Nat. Genet. https://doi.org/10.1038/s41588-022-01179-9 (2022).

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Somatic mosaicism rewires transcriptional and epigenetic states in clonal hematopoiesis. Nat Genet 54, 1453–1454 (2022). https://doi.org/10.1038/s41588-022-01181-1

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