» Articles » PMID: 29723958

The Vast Complexity of the Epigenetic Landscape During Neurodevelopment: An Open Frame to Understanding Brain Function

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2018 May 5
PMID 29723958
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Development is a well-defined stage-to-stage process that allows the coordination and maintenance of the structure and function of cells and their progenitors, in a complete organism embedded in an environment that, in turn, will shape cellular responses to external stimuli. Epigenetic mechanisms comprise a group of process that regulate genetic expression without changing the DNA sequence, and they contribute to the necessary plasticity of individuals to face a constantly changing medium. These mechanisms act in conjunction with genetic pools and their correct interactions will be crucial to zygote formation, embryo development, and brain tissue organization. In this work, we will summarize the main findings related to DNA methylation and histone modifications in embryonic stem cells and throughout early development phases. Furthermore, we will critically outline some key observations on how epigenetic mechanisms influence the rest of the developmental process and how long its footprint is extended from fecundation to adulthood.

Citing Articles

Mitochondrial supplementation of Sus scrofa metaphase II oocytes alters DNA methylation and gene expression profiles of blastocysts.

Okada T, McIlfatrick S, Hin N, Aryamanesh N, Breen J, St John J Epigenetics Chromatin. 2022; 15(1):12.

PMID: 35428319 PMC: 9013150. DOI: 10.1186/s13072-022-00442-x.


Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders.

Velasco G, Ulveling D, Rondeau S, Marzin P, Unoki M, Cormier-Daire V Int J Mol Sci. 2021; 22(7).

PMID: 33916664 PMC: 8038329. DOI: 10.3390/ijms22073735.


Maternal Protein Restriction in Rats Alters the Expression of Genes Involved in Mitochondrial Metabolism and Epitranscriptomics in Fetal Hypothalamus.

Frapin M, Guignard S, Meistermann D, Grit I, Moulle V, Paille V Nutrients. 2020; 12(5).

PMID: 32438566 PMC: 7284977. DOI: 10.3390/nu12051464.


Differential Methylation of H3K79 Reveals DOT1L Target Genes and Function in the Cerebellum In Vivo.

Bovio P, Franz H, Heidrich S, Rauleac T, Kilpert F, Manke T Mol Neurobiol. 2018; 56(6):4273-4287.

PMID: 30302725 PMC: 6505521. DOI: 10.1007/s12035-018-1377-1.


Epigenetics of Neurodevelopmental Disorders Comes of Age with Roles in Clinical and Educational Applications.

Kubota T Int J Mol Sci. 2018; 19(9).

PMID: 30213026 PMC: 6163238. DOI: 10.3390/ijms19092720.

References
1.
Han J, Kim H, Schafer S, Paquola A, Clemenson G, Toda T . Functional Implications of miR-19 in the Migration of Newborn Neurons in the Adult Brain. Neuron. 2016; 91(1):79-89. DOI: 10.1016/j.neuron.2016.05.034. View

2.
Adlakha Y, Saini N . Brain microRNAs and insights into biological functions and therapeutic potential of brain enriched miRNA-128. Mol Cancer. 2014; 13:33. PMC: 3936914. DOI: 10.1186/1476-4598-13-33. View

3.
Ramsahoye B, Biniszkiewicz D, Lyko F, Clark V, Bird A, Jaenisch R . Non-CpG methylation is prevalent in embryonic stem cells and may be mediated by DNA methyltransferase 3a. Proc Natl Acad Sci U S A. 2000; 97(10):5237-42. PMC: 25812. DOI: 10.1073/pnas.97.10.5237. View

4.
Bell J, Tsai P, Yang T, Pidsley R, Nisbet J, Glass D . Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population. PLoS Genet. 2012; 8(4):e1002629. PMC: 3330116. DOI: 10.1371/journal.pgen.1002629. View

5.
Kundaje A, Meuleman W, Ernst J, Bilenky M, Yen A, Heravi-Moussavi A . Integrative analysis of 111 reference human epigenomes. Nature. 2015; 518(7539):317-30. PMC: 4530010. DOI: 10.1038/nature14248. View