NONO promotes MYB expression and splicing by interacting with enhancer lncRNA MY34UE ‐ AS in human leukemia cells
Abstract
Dysregulation of the transcription factor MYB plays a critical role in leukemia pathogenesis, progression, and prognosis; however, the detailed regulatory mechanisms of MYB remain unclear. Recently, we identified an enhancer long noncoding RNA (lncRNA) MY34UE-AS, which upregulates MYB expression. Here, we demonstrate that non-POU-domain-containing octamer binding protein (NONO) binds to MY34UE-AS through its RNA recognition motif 2 (RRM2) domain, thereby upregulating MYB expression and splicing. This interaction drives leukemia cell proliferation and migration. Our findings unveil a novel regulatory mechanism of MYB and propose the NONO-MY34UE-AS axis as a potential therapeutic target for leukemia. Impact statement Our study uncovers the NONO-MY34UE-AS-MYB regulatory axis in leukemia, revealing a new layer of MYB control. This mechanistic insight advances understanding of oncogenic transcription factor dysregulation and highlights potential therapeutic targets, offering new directions for leukemia research.
Fields of Study & Subjects
Cancer-related molecular mechanisms research
RNA Research and Splicing
Genomics and Chromatin Dynamics
Publication details
- Journal / source
- FEBS Letters
- Volume
- 600
- Issue
- 7
- Pages
- 1062–1072
- Publication date
- 10 March 2026
- Language
- EN