Abstract 2283 Modulation of Super-Enhancer Activity in T-ALL JURKAT Cells Utilizing Synthetic Zinc Finger Proteins

Tight regulation of gene expression is mandatory for efficient cellular differentiation and the prevention of oncogenesis. When genes become dysregulated it can lead to differentiation blockades and abnormal cellular proliferation. A common avenue of gene dysregulation is the modulation of enhancer activity that leads to high-level, aberrant expression of oncogenes. A subset of T-cell Acute Lymphoblastic Leukemia (T-ALL) is characterized by an insertional mutation upstream of the T-cell Acute Lymphocytic Leukemia Protein 1 (TAL1) gene locus that creates a de novo binding site for c-MYB, a transcription factor, that in-turn recruits a multitude of other transcription factors to form a super-enhancer complex.

Authors

Institutions

Publication Details

Journal
Journal of Biological Chemistry
Published
2025-05-01
DOI
https://doi.org/10.1016/j.jbc.2025.109285
Primary Topic
RNA Interference and Gene Delivery
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 2283 Modulation of Super-Enhancer Activity in T-ALL JURKAT Cells Utilizing Synthetic Zinc Finger Proteins

Eliot M. Gunn, Gregory A. Hudalla, Leonardo Martín Pérez, Vincent Nganga et al.
Journal of Biological Chemistry
RNA Interference and Gene Delivery
article

Abstract 2283 Modulation of Super-Enhancer Activity in T-ALL JURKAT Cells Utilizing Synthetic Zinc Finger Proteins

Eliot M. Gunn, Gregory A. Hudalla, Leonardo Martín Pérez, Vincent Nganga, Jörg Bungert, M. Gibbons, Niko Linzer, Eugene M. Oltz, Mir Ahamed Hossain
article en

Abstract

Tight regulation of gene expression is mandatory for efficient cellular differentiation and the prevention of oncogenesis. When genes become dysregulated it can lead to differentiation blockades and abnormal cellular proliferation. A common avenue of gene dysregulation is the modulation of enhancer activity that leads to high-level, aberrant expression of oncogenes. A subset of T-cell Acute Lymphoblastic Leukemia (T-ALL) is characterized by an insertional mutation upstream of the T-cell Acute Lymphocytic Leukemia Protein 1 (TAL1) gene locus that creates a de novo binding site for c-MYB, a transcription factor, that in-turn recruits a multitude of other transcription factors to form a super-enhancer complex.

Journal of Biological ChemistryVol. 301(5)
University of Florida Health (US), University of Florida (US)
Zero hunger
Openalex Percentile: Top 88%
RNA Interference and Gene Delivery
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Abstract 2283 Modulation of Super-Enhancer Activity in T-ALL JURKAT Cells Utilizing Synthetic Zinc Finger Proteins — Eliot M. Gunn, Gregory A. Hudalla, et al. · Journal of Biological Chemistry (2025) | TGRS Research Map | TGRS