Ausió Juan
Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC V8W 3P6 Canada.
Clin Epigenetics. 2016 May 21;8:58. doi: 10.1186/s13148-016-0214-5. eCollection 2016.
Methyl CpG binding protein 2 (MeCP2) is a highly abundant chromosomal protein within the brain. It is hence not surprising that perturbations in its genome-wide distribution, and at particular loci within this tissue, can result in widespread neurological disorders that transcend the early implications of this protein in Rett syndrome (RTT). Yet, the details of its role and involvement in chromatin organization are still poorly understood. This paper focuses on what is known to date about all of this with special emphasis on the relation to different epigenetic modifications (DNA methylation, histone acetylation/ubiquitination, MeCP2 phosphorylation and miRNA). We showcase all of the above in two particular important neurological functional alterations in the brain: depression (major depressive disorder [MDD]) and cocaine addiction, both of which affect the MeCP2 homeostasis and result in significant changes in the overall levels of these epigenetic marks.
甲基化CpG结合蛋白2(MeCP2)是大脑中一种高度丰富的染色体蛋白。因此,其全基因组分布的扰动,特别是在该组织内的特定基因座处的扰动,会导致广泛的神经系统疾病,这超越了该蛋白在雷特综合征(RTT)中的早期影响,也就不足为奇了。然而,其在染色质组织中的作用和参与的细节仍知之甚少。本文重点关注迄今为止关于所有这些方面的已知情况,特别强调与不同表观遗传修饰(DNA甲基化、组蛋白乙酰化/泛素化、MeCP2磷酸化和微小RNA)的关系。我们在大脑中两种特别重要的神经功能改变中展示了上述所有内容:抑郁症(重度抑郁症[MDD])和可卡因成瘾,这两种情况都会影响MeCP2的稳态,并导致这些表观遗传标记的总体水平发生显著变化。