Please use this identifier to cite or link to this item: https://doi.org/10.15252/msb.20177754
Title: RNA polymerase II primes Polycomb-repressed developmental genes throughout terminal neuronal differentiation
Authors: Ferrai, C
Torlai Triglia, E
Risner-Janiczek, J.R
Rito, T
Rackham, O.J.L 
de Santiago, I
Kukalev, A
Nicodemi, M
Akalin, A
Li, M
Ungless, M.A
Pombo, A
Keywords: DNA
hepatocyte nuclear factor 3beta
neurogenin 2
octamer transcription factor 4
polycomb repressive complex 2
RNA polymerase II
semaphorin 3F
transcription factor Mash1
polycomb group protein
RNA polymerase II
transcription factor
Article
cell maturation
chromatin
developmental gene
DNA methylation
DNA replication
dopaminergic nerve cell
electrophysiology
frontal cortex
human
inhibition kinetics
mesencephalon
molecular dynamics
nerve cell culture
nerve cell differentiation
nerve cell plasticity
nonhuman
phenotype
pluripotent stem cell
priority journal
promoter region
protein expression
animal
cell differentiation
cytology
genetics
metabolism
mouse
mouse embryonic stem cell
sequence analysis
Animals
Cell Differentiation
Dopaminergic Neurons
Genes, Developmental
Mice
Mouse Embryonic Stem Cells
Polycomb-Group Proteins
Promoter Regions, Genetic
RNA Polymerase II
Sequence Analysis, RNA
Transcription Factors
Issue Date: 2017
Citation: Ferrai, C, Torlai Triglia, E, Risner-Janiczek, J.R, Rito, T, Rackham, O.J.L, de Santiago, I, Kukalev, A, Nicodemi, M, Akalin, A, Li, M, Ungless, M.A, Pombo, A (2017). RNA polymerase II primes Polycomb-repressed developmental genes throughout terminal neuronal differentiation. Molecular Systems Biology 13 (10) : 946. ScholarBank@NUS Repository. https://doi.org/10.15252/msb.20177754
Rights: Attribution 4.0 International
Abstract: Polycomb repression in mouse embryonic stem cells (ESCs) is tightly associated with promoter co-occupancy of RNA polymerase II (RNAPII) which is thought to prime genes for activation during early development. However, it is unknown whether RNAPII poising is a general feature of Polycomb repression, or is lost during differentiation. Here, we map the genome-wide occupancy of RNAPII and Polycomb from pluripotent ESCs to non-dividing functional dopaminergic neurons. We find that poised RNAPII complexes are ubiquitously present at Polycomb-repressed genes at all stages of neuronal differentiation. We observe both loss and acquisition of RNAPII and Polycomb at specific groups of genes reflecting their silencing or activation. Strikingly, RNAPII remains poised at transcription factor genes which are silenced in neurons through Polycomb repression, and have major roles in specifying other, non-neuronal lineages. We conclude that RNAPII poising is intrinsically associated with Polycomb repression throughout differentiation. Our work suggests that the tight interplay between RNAPII poising and Polycomb repression not only instructs promoter state transitions, but also may enable promoter plasticity in differentiated cells. @ 2017 The Authors. Published under the terms of the CC BY 4.0 license
Source Title: Molecular Systems Biology
URI: https://scholarbank.nus.edu.sg/handle/10635/179455
ISSN: 17444292
DOI: 10.15252/msb.20177754
Rights: Attribution 4.0 International
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