Literature DB >> 21264459

[Epigenetic mechanisms in major depression].

G Paslakis1, S Bleich, H Frieling, M Deuschle.   

Abstract

The term epigenetics describes mechanisms that can change the function of genes in the absence of an alteration of the actual DNA sequence. Among others, histone protein modifications (methylation, acetylation and phosphorylation) and DNA methylation constitute epigenetic mechanisms. Histone methylation and histone deacetylation in promoter regions of neurotrophic factors that have been associated with depression lead to their reduced expression. The methylation of DNA in promoter regions of genes coding for receptors and neurotrophic factors also results in their reduced expression, as was revealed for depressive disorders. Preclinical studies have shown that maternal care has a crucial influence on the reactivity of the hypothalamic-pituitary-adrenocortical axis of the offspring due to epigenetic mechanisms. These are acquired modifications that can be partially reversed by drug treatment (antidepressants).

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Year:  2011        PMID: 21264459     DOI: 10.1007/s00115-010-3200-8

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  52 in total

Review 1.  Epigenetic reprogramming in mammals.

Authors:  Hugh D Morgan; Fátima Santos; Kelly Green; Wendy Dean; Wolf Reik
Journal:  Hum Mol Genet       Date:  2005-04-15       Impact factor: 6.150

Review 2.  The mesolimbic dopamine reward circuit in depression.

Authors:  Eric J Nestler; William A Carlezon
Journal:  Biol Psychiatry       Date:  2006-03-29       Impact factor: 13.382

Review 3.  Functions of site-specific histone acetylation and deacetylation.

Authors:  Mona D Shahbazian; Michael Grunstein
Journal:  Annu Rev Biochem       Date:  2007       Impact factor: 23.643

Review 4.  Epigenetic regulation in psychiatric disorders.

Authors:  Nadia Tsankova; William Renthal; Arvind Kumar; Eric J Nestler
Journal:  Nat Rev Neurosci       Date:  2007-05       Impact factor: 34.870

5.  Why females are mosaics, X-chromosome inactivation, and sex differences in disease.

Authors:  Barbara R Migeon
Journal:  Gend Med       Date:  2007-06

Review 6.  Eukaryotic cytosine methyltransferases.

Authors:  Mary Grace Goll; Timothy H Bestor
Journal:  Annu Rev Biochem       Date:  2005       Impact factor: 23.643

7.  DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development.

Authors:  M Okano; D W Bell; D A Haber; E Li
Journal:  Cell       Date:  1999-10-29       Impact factor: 41.582

Review 8.  Neurodevelopmental sequelae of postnatal maternal care in rodents: clinical and research implications of molecular insights.

Authors:  Arie Kaffman; Michael J Meaney
Journal:  J Child Psychol Psychiatry       Date:  2007 Mar-Apr       Impact factor: 8.982

9.  GABAA receptor promoter hypermethylation in suicide brain: implications for the involvement of epigenetic processes.

Authors:  Michael O Poulter; Lisheng Du; Ian C G Weaver; Miklós Palkovits; Gábor Faludi; Zul Merali; Moshe Szyf; Hymie Anisman
Journal:  Biol Psychiatry       Date:  2008-07-18       Impact factor: 13.382

Review 10.  Strategy for investigating interactions between measured genes and measured environments.

Authors:  Terrie E Moffitt; Avshalom Caspi; Michael Rutter
Journal:  Arch Gen Psychiatry       Date:  2005-05
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