Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012 Aug;4(4):445-57.
doi: 10.2217/epi.12.37.

Sensitive periods in epigenetics: bringing us closer to complex behavioral phenotypes

Affiliations
Review

Sensitive periods in epigenetics: bringing us closer to complex behavioral phenotypes

Corina Nagy et al. Epigenomics. 2012 Aug.

Abstract

Genetic studies have attempted to elucidate causal mechanisms for the development of complex disease, but genome-wide associations have been largely unsuccessful in establishing these links. As an alternative link between genes and disease, recent efforts have focused on mechanisms that alter the function of genes without altering the underlying DNA sequence. Known as epigenetic mechanisms, these include DNA methylation, chromatin conformational changes through histone modifications, ncRNAs and, most recently, 5-hydroxymethylcytosine. Although DNA methylation is involved in normal development, aging and gene regulation, altered methylation patterns have been associated with disease. It is generally believed that early life constitutes a period during which there is increased sensitivity to the regulatory effects of epigenetic mechanisms. The purpose of this review is to outline the contribution of epigenetic mechanisms to genomic function, particularly in the development of complex behavioral phenotypes, focusing on the sensitive periods.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Klein Rj, Zeiss C, Chew Ey, et al. Complement factor H polymorphism in age-related macular degeneration. Science. 2005;308(5720):385–389. - PMC - PubMed
    1. Craddock N, O’donovan M, Owen M. The genetics of schizophrenia and bipolar disorder: dissecting psychosis. Journal of medical genetics. 2005;42:193–397. 7f574d8c-e56e-2298-a727-61a20bc912a4. - PMC - PubMed
    1. Harrison P, Weinberger D. Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence. Molecular psychiatry. 2005;10:40. be238ca9-b847-311a-634c-9a356152c8c4. - PubMed
    1. Li Y, Ding G, Booth, et al. Sensitive period for white-matter connectivity of superior temporal cortex in deaf people. Human Brain Mapping. 2012;33(2):349–359. - PMC - PubMed
    1. Pimperton H, Kennedy Cr. The impact of early identification of permanent childhood hearing impairment on speech and language outcomes. Archives of Disease in Childhood. 2012 - PubMed

Publication types