Transposable Elements Shape Stemness in Normal and Leukemic Hematopoiesis

Abstract

Despite most acute myeloid leukemia (AML) patients achieving complete remission after induction chemotherapy, two thirds of patients will relapse with fatal disease within 5 years. AML is organized as a cellular hierarchy sustained by leukemia stem cells (LSC) at the apex, with LSC properties directly linked to tumor progression, therapy failure and disease relapse 1-5. Despite the central role of LSC in poor patient outcomes, little is known of the genetic determinants of their stemness properties 6-8. Although much AML research focuses on mutational processes and their impact on gene expression programs, the genetic determinants of cell state properties including stemness expand beyond mutations, relying on the genetic architecture captured in the chromatin of each cell 9-11. As LSCs share many functional and molecular properties with normal hematopoietic stem cells (HSC), we identified genetic determinants of primitive populations enriched for LSCs and HSCs in comparison with their downstream mature progeny by investigating their chromatin accessibility. Our work reveals how distinct transposable element (TE) subfamilies are used in primitive versus mature populations, functioning as docking sites for stem cell-associated regulators of genome topology, including CTCF, or lineage-specific transcription regulators in primitive and mature populations, respectively. We further show how TE subfamilies accessible in LSCs define docking sites for several oncogenic drivers in AML, namely FLI1, LYL1 and MEIS1. Using chromatin accessibility profiles from a cohort of AML patients, we further show the clinical utility of our TE accessibility-based LSCTE121 scoring scheme to identify patients with high rates of relapse. Collectively, our work reveals how different accessible TE subfamilies serve as genetic determinants of stemness properties in normal and leukemic hematopoietic stem cells.

Transposable elements in normal and malignant hematopoiesis

“…AML is often associated with epigenetic alterations in DNA methylation and modification of histones. In a 2021 preprint, Nadorp et al revealed that LSCs and mature leukemic cells display different chromatin accessibility profiles for diverse TE subfamilies ( Nadorp et al, 2021 preprint). Interestingly, TEs located in the accessible chromatin of LSCs act as docking sites for several oncogenic drivers of AML, including LYL1, a proto-oncogene of the TAL family ( Nadorp et al, 2021 ).…”

“…In a 2021 preprint, Nadorp et al revealed that LSCs and mature leukemic cells display different chromatin accessibility profiles for diverse TE subfamilies ( Nadorp et al, 2021 preprint). Interestingly, TEs located in the accessible chromatin of LSCs act as docking sites for several oncogenic drivers of AML, including LYL1, a proto-oncogene of the TAL family ( Nadorp et al, 2021 ). By contrast, a large proportion of the TE pool is repressed by methylation in AML ( Capone et al, 2018 ).…”