Figure 4.
Roles of other RNA modifications in normal and malignant hematopoiesis. In addition to m6A, other RNA modifications, such as A-to-I editing, m5C, and pseudouridine (ψ), are implicated in normal and malignant hematopoiesis. Specifically, ψ synthase is essential for efficient HSC differentiation, and ψ is highly excreted in urine in AML and chronic myeloid leukemia (CML). Increased levels of m5C and its writers confer chemoresistance to MDS/AML cells, m5C writers are positively associated with MDS/AML progression, and m5C eraser TET2 promotes infection-induced myelopoiesis. The writer for A-to-I editing is required for maintenance of HSCs and survival of hematopoietic progenitor cell (HPCs), whereas the same writer promotes transformation of myeloid progenitors into LSCs/LICs and enhances LSC/LIC self-renewal activity. The level of A-to-I editing is positively correlated with CML progression.

Roles of other RNA modifications in normal and malignant hematopoiesis. In addition to m6A, other RNA modifications, such as A-to-I editing, m5C, and pseudouridine (ψ), are implicated in normal and malignant hematopoiesis. Specifically, ψ synthase is essential for efficient HSC differentiation, and ψ is highly excreted in urine in AML and chronic myeloid leukemia (CML). Increased levels of m5C and its writers confer chemoresistance to MDS/AML cells, m5C writers are positively associated with MDS/AML progression, and m5C eraser TET2 promotes infection-induced myelopoiesis. The writer for A-to-I editing is required for maintenance of HSCs and survival of hematopoietic progenitor cell (HPCs), whereas the same writer promotes transformation of myeloid progenitors into LSCs/LICs and enhances LSC/LIC self-renewal activity. The level of A-to-I editing is positively correlated with CML progression.

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