Minocherhomji Sheroy, Hansen Claus, Kim Hyung-Goo, Mang Yuan, Bak Mads, Guldberg Per, Papadopoulos Nickolas, Eiberg Hans, Doh Gerald Dayebga, Møllgård Kjeld, Hertz Jens Michael, Nielsen Jørgen E, Ropers Hans-Hilger, Tümer Zeynep, Tommerup Niels, Kalscheuer Vera M, Silahtaroglu Asli
Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, Faculty of Health Sciences, University of Copenhagen, Copenhagen N DK-2200, Denmark.
Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin 14195, Germany.
Hum Mol Genet. 2014 Dec 1;23(23):6163-76. doi: 10.1093/hmg/ddu337. Epub 2014 Jul 1.
Genome instability, epigenetic remodelling and structural chromosomal rearrangements are hallmarks of cancer. However, the coordinated epigenetic effects of constitutional chromosomal rearrangements that disrupt genes associated with congenital neurodevelopmental diseases are poorly understood. To understand the genetic-epigenetic interplay at breakpoints of chromosomal translocations disrupting CG-rich loci, we quantified epigenetic modifications at DLGAP4 (SAPAP4), a key post-synaptic density 95 (PSD95) associated gene, truncated by the chromosome translocation t(8;20)(p12;q11.23), co-segregating with cerebellar ataxia in a five-generation family. We report significant epigenetic remodelling of the DLGAP4 locus triggered by the t(8;20)(p12;q11.23) translocation and leading to dysregulation of DLGAP4 expression in affected carriers. Disruption of DLGAP4 results in monoallelic hypermethylation of the truncated DLGAP4 promoter CpG island. This induced hypermethylation is maintained in somatic cells of carriers across several generations in a t(8;20) dependent-manner however, is erased in the germ cells of the translocation carriers. Subsequently, chromatin remodelling of the locus-perturbed monoallelic expression of DLGAP4 mRNAs and non-coding RNAs in haploid cells having the translocation. Our results provide new mechanistic insight into the way a balanced chromosomal rearrangement associated with a neurodevelopmental disorder perturbs allele-specific epigenetic mechanisms at breakpoints leading to the deregulation of the truncated locus.
基因组不稳定、表观遗传重塑和染色体结构重排是癌症的标志。然而,对于破坏与先天性神经发育疾病相关基因的构成性染色体重排的协同表观遗传效应,我们了解甚少。为了理解在破坏富含CG位点的染色体易位断点处的遗传-表观遗传相互作用,我们对DLGAP4(SAPAP4)进行了表观遗传修饰定量分析,DLGAP4是一个与突触后致密物95(PSD95)相关的关键基因,在一个五代家族中因染色体易位t(8;20)(p12;q11.23)而被截断,并与小脑共济失调共分离。我们报告了由t(8;20)(p12;q11.23)易位引发的DLGAP4基因座显著表观遗传重塑,导致受影响携带者中DLGAP4表达失调。DLGAP4的破坏导致截断的DLGAP4启动子CpG岛单等位基因高甲基化。这种诱导的高甲基化以t(8;20)依赖的方式在携带者的体细胞中跨几代维持,然而,在易位携带者的生殖细胞中被消除。随后,该基因座的染色质重塑扰乱了具有易位的单倍体细胞中DLGAP4 mRNA和非编码RNA的单等位基因表达。我们的结果为与神经发育障碍相关的平衡染色体重排在断点处扰乱等位基因特异性表观遗传机制从而导致截断基因座失调的方式提供了新的机制见解。