The enhancer RNA ARIEL activates the oncogenic transcriptional program in T-cell acute lymphoblastic leukemia.
Shi Hao TanWei Zhong LeongPhuong Cao Thi NgocTze King TanFatima Carla BertulfoMei Chee LimOmer AnZhenhua LiAllen Eng-Juh YeohMelissa J FullwoodDaniel G TenenTakaomi SandaPublished in: Blood (2019)
The oncogenic transcription factor TAL1 regulates the transcriptional program in T-ALL. ARID5B is one of the critical downstream targets of TAL1, which further activates the oncogenic regulatory circuit in T-ALL cells. Here, we elucidated the molecular functions of the noncoding RNA, ARID5B-inducing enhancer associated long noncoding RNA (ARIEL), in T-ALL pathogenesis. We demonstrated that ARIEL is specifically activated in TAL1 + T-ALL cases, and its expression is associated with ARID5B enhancer activity. ARIEL recruits mediator proteins to the ARID5B enhancer, promotes enhancer-promoter interactions, and activates the expression of ARID5B, thereby positively regulating the TAL1-induced transcriptional program and the MYC oncogene. The TAL1 complex coordinately regulates the expression of ARIEL Knockdown of ARIEL inhibits cell growth and survival of T-ALL cells in culture and blocks disease progression in a murine xenograft model. Our results indicate that ARIEL plays an oncogenic role as an enhancer RNA in T-ALL.
Keyphrases
- transcription factor
- poor prognosis
- dna binding
- long noncoding rna
- acute lymphoblastic leukemia
- binding protein
- induced apoptosis
- quality improvement
- cell cycle arrest
- genome wide identification
- oxidative stress
- cell death
- dna methylation
- cell proliferation
- allogeneic hematopoietic stem cell transplantation
- endothelial cells
- heat stress
- pi k akt