Back to Search
Start Over
Targeted Enhancer Activation by a Subunit of the Integrator Complex.
- Source :
-
Molecular cell [Mol Cell] 2018 Jul 05; Vol. 71 (1), pp. 103-116.e7. Date of Electronic Publication: 2018 Jun 28. - Publication Year :
- 2018
-
Abstract
- The control of cell fate is an epigenetic process initiated by transcription factors (TFs) that recognize DNA motifs and recruit activator complexes and transcriptional machineries to chromatin. Lineage specificity is thought to be provided solely by TF-motif pairing, while the recruited activators are passive. Here, we show that INTS13, a subunit of the Integrator complex, operates as monocytic/macrophagic differentiation factor. Integrator is a general activator of transcription at coding genes and is required for eRNA maturation. Here, we show that INTS13 functions as an independent sub-module and targets enhancers through Early Growth Response (EGR1/2) TFs and their co-factor NAB2. INTS13 binds poised monocytic enhancers eliciting chromatin looping and activation. Independent depletion of INTS13, EGR1, or NAB2 impairs monocytic differentiation of cell lines and primary human progenitors. Our data demonstrate that Integrator is not functionally homogeneous and has TF-specific regulatory potential, revealing a new enhancer regulatory axis that controls myeloid differentiation.<br /> (Copyright © 2018 Elsevier Inc. All rights reserved.)
- Subjects :
- Cell Line
Early Growth Response Protein 1 genetics
Early Growth Response Protein 2 genetics
Humans
Myeloid Progenitor Cells cytology
Repressor Proteins genetics
Cell Differentiation
Early Growth Response Protein 1 metabolism
Early Growth Response Protein 2 metabolism
Enhancer Elements, Genetic
Monocytes metabolism
Myeloid Progenitor Cells metabolism
Repressor Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 71
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 30008316
- Full Text :
- https://doi.org/10.1016/j.molcel.2018.05.031