Nature communications · 2026
Single cell transcriptional evolution of myeloid leukemia of Down syndrome.
СтатьяНазвание и аннотация: Перевод в очереди
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Trinh Mi K, Schuschel Konstantin, Issa Hasan, Thomas Rebecca, Parks Conor, Oszlanczi Agnes, Ogbonnah Toochi, Zhou Di, Mamanova Lira, Prigmore Elena, Robertson Emilia R, Hodder Angus, Wenger Anna, Anderson Nathaniel D, Whitfield Holly J, Treger Taryn D, Gonçalves-Dias José, Straathof Karin, O'Connor David, Young Matthew D, Jardine Laura, Adams Stuart, Klusmann Jan-Henning, Bartram Jack, Behjati Sam
Аннотация
Children with Down syndrome have a 150-fold increased risk of developing myeloid leukaemia (ML-DS). Unusually for a childhood leukaemia, ML-DS arises from a preleukaemic state, termed transient abnormal myelopoiesis (TAM), via a conserved sequence of mutations. Here, we examine the relationship between the genetic and transcriptional evolution of ML-DS from natural variation; a rich collection of primary patient samples and foetal tissues with a range of constitutional karyotypes. We distil transcriptional consequences of each genetic step in ML-DS evolution, utilising single-cell mRNA sequencing, complemented by phylogenetic analyses in progressive disease. We find that transcriptional changes induced by the TAM-defining GATA1 mutations are retained in, and account for most of the ML-DS transcriptome. The GATA1 transcriptome pervades all stages of ML-DS, including progressive disease that had undergone genetic evolution. Our approach delineates the transcriptional evolution of ML-DS and provides an analytical blueprint for distiling consequences of mutations within their pathophysiological context.