» Articles » PMID: 38412562

Epigenetic Control and Manipulation of Neuronal Maturation Timing

Overview
Publisher Elsevier
Specialties Biology
Genetics
Date 2024 Feb 27
PMID 38412562
Authors
Affiliations
Soon will be listed here.
Abstract

During brain development, the sequence of developmental steps and the underlying transcriptional regulatory logic are largely conserved across species. However, the temporal unfolding of developmental programs varies dramatically across species and within a given species varies across brain regions and cell identities. The maturation of neurons in the human cerebral cortex is particularly slow and lasts for many years compared with only a few weeks for the corresponding mouse neurons. The mechanisms setting the 'schedule' of neuronal maturation remain unclear but appear to be linked to a cell-intrinsic 'clock'. Here, we discuss recent findings that highlight a role for epigenetic factors in the timing of neuronal maturation. Manipulations of those factors in stem cell-based models can override the intrinsic pace of neuronal maturation, including its protracted nature in human cortical neurons. We then contextualize the epigenetic regulation of maturation programs with findings from other model systems and propose potential interactions between epigenetic pathways and other drivers of developmental rates.

Citing Articles

Reflections on the Role of Differentiation Processes in Forming Behavioral Phenotypes: Can These Processes Replace the Concepts of Plastic Phenotype and Reversible Plastic Phenotype?.

Chiappa P Biology (Basel). 2025; 14(2).

PMID: 40001955 PMC: 11852096. DOI: 10.3390/biology14020187.


Multiplexed CRISPRi Reveals a Transcriptional Switch Between KLF Activators and Repressors in the Maturing Neocortex.

Kirk R, Sun L, Xiao R, Clark E, Nelson S bioRxiv. 2025; .

PMID: 39975013 PMC: 11839100. DOI: 10.1101/2025.02.07.636951.


Consequences of trisomy 21 for brain development in Down syndrome.

Russo M, Sousa A, Bhattacharyya A Nat Rev Neurosci. 2024; 25(11):740-755.

PMID: 39379691 PMC: 11834940. DOI: 10.1038/s41583-024-00866-2.

References
1.
Rhee H, Closser M, Guo Y, Bashkirova E, Tan G, Gifford D . Expression of Terminal Effector Genes in Mammalian Neurons Is Maintained by a Dynamic Relay of Transient Enhancers. Neuron. 2016; 92(6):1252-1265. PMC: 5193225. DOI: 10.1016/j.neuron.2016.11.037. View

2.
Appiah B, Fullio C, Ossola C, Bertani I, Restelli E, Cheffer A . DOT1L activity affects neural stem cell division mode and reduces differentiation and ASNS expression. EMBO Rep. 2023; 24(8):e56233. PMC: 10398646. DOI: 10.15252/embr.202256233. View

3.
Hickey S, Berto S, Konopka G . Chromatin Decondensation by FOXP2 Promotes Human Neuron Maturation and Expression of Neurodevelopmental Disease Genes. Cell Rep. 2019; 27(6):1699-1711.e9. PMC: 6794152. DOI: 10.1016/j.celrep.2019.04.044. View

4.
Matlik K, Govek E, Paul M, Allis C, Hatten M . Histone bivalency regulates the timing of cerebellar granule cell development. Genes Dev. 2023; 37(13-14):570-589. PMC: 10499015. DOI: 10.1101/gad.350594.123. View

5.
Agarwal S, Bonefas K, Garay P, Brookes E, Murata-Nakamura Y, Porter R . KDM1A maintains genome-wide homeostasis of transcriptional enhancers. Genome Res. 2021; 31(2):186-197. PMC: 7849409. DOI: 10.1101/gr.234559.118. View