HyperTRIBE uncovers increased MUSASHI-2 RNA binding activity and differential regulation in leukemic stem cells.

Publication Type Academic Article
Authors Nguyen D, Lu Y, Chu E, Yang X, Park S, Choo Z, Chin C, Prieto C, Schurer A, Barin E, Savino A, Gourkanti S, Patel P, Vu L, Leslie C, Kharas M
Journal Nat Commun
Volume 11
Issue 1
Pagination 2026
Date Published 04/24/2020
ISSN 2041-1723
Keywords Cell Differentiation, Hematopoietic Stem Cells, Leukemia, Neoplastic Stem Cells, RNA-Binding Proteins
Abstract The cell-context dependency for RNA binding proteins (RBPs) mediated control of stem cell fate remains to be defined. Here we adapt the HyperTRIBE method using an RBP fused to a Drosophila RNA editing enzyme (ADAR) to globally map the mRNA targets of the RBP MSI2 in mammalian adult normal and malignant stem cells. We reveal a unique MUSASHI-2 (MSI2) mRNA binding network in hematopoietic stem cells that changes during transition to multipotent progenitors. Additionally, we discover a significant increase in RNA binding activity of MSI2 in leukemic stem cells compared with normal hematopoietic stem and progenitor cells, resulting in selective regulation of MSI2's oncogenic targets. This provides a basis for MSI2 increased dependency in leukemia cells compared to normal cells. Moreover, our study provides a way to measure RBP function in rare cells and suggests that RBPs can achieve differential binding activity during cell state transition independent of gene expression.
DOI 10.1038/s41467-020-15814-8
PubMed ID 32332729
PubMed Central ID PMC7181745
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