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肾上腺脑白质营养不良的表观基因组特征预示着少突胶质细胞分化受损。

Epigenomic signature of adrenoleukodystrophy predicts compromised oligodendrocyte differentiation.

机构信息

Neurometabolic Diseases Laboratory, Bellvitge Biomedical Research Institute (IDIBELL), 08908 L'Hospitalet de Llobregat, Barcelona, Spain.

Center for Biomedical Research on Rare Diseases (CIBERER), ISCIII, Spain.

出版信息

Brain Pathol. 2018 Nov;28(6):902-919. doi: 10.1111/bpa.12595. Epub 2018 Apr 10.

Abstract

Epigenomic changes may either cause disease or modulate its expressivity, adding a layer of complexity to mendelian diseases. X-linked adrenoleukodystrophy (X-ALD) is a rare neurometabolic condition exhibiting discordant phenotypes, ranging from a childhood cerebral inflammatory demyelination (cALD) to an adult-onset mild axonopathy in spinal cords (AMN). The AMN form may occur with superimposed inflammatory brain demyelination (cAMN). All patients harbor loss of function mutations in the ABCD1 peroxisomal transporter of very-long chain fatty acids. The factors that account for the lack of genotype-phenotype correlation, even within the same family, remain largely unknown. To gain insight into this matter, here we compared the genome-wide DNA methylation profiles of morphologically intact frontal white matter areas of children affected by cALD with adult cAMN patients, including male controls in the same age group. We identified a common methylomic signature between the two phenotypes, comprising (i) hypermethylation of genes harboring the H3K27me3 mark at promoter regions, (ii) hypermethylation of genes with major roles in oligodendrocyte differentiation such as MBP, CNP, MOG and PLP1 and (iii) hypomethylation of immune-associated genes such as IFITM1 and CD59. Moreover, we found increased hypermethylation in CpGs of genes involved in oligodendrocyte differentiation, and also in genes with H3K27me3 marks in their promoter regions in cALD compared with cAMN, correlating with transcriptional and translational changes. Further, using a penalized logistic regression model, we identified the combined methylation levels of SPG20, UNC45A and COL9A3 and also, the combined expression levels of ID4 and MYRF to be good markers capable of discriminating childhood from adult inflammatory phenotypes. We thus propose the hypothesis that an epigenetically controlled, altered transcriptional program may drive an impaired oligodendrocyte differentiation and aberrant immune activation in X-ALD patients. These results shed light into disease pathomechanisms and uncover putative biomarkers of interest for prognosis and phenotypic stratification.

摘要

表观遗传变化既可以导致疾病,也可以调节其表现度,为孟德尔疾病增加了一层复杂性。X 连锁肾上腺脑白质营养不良(X-ALD)是一种罕见的神经代谢疾病,表现出不同的表型,从儿童脑炎性脱髓鞘(cALD)到成人发病的脊髓轴索病(AMN)。AMN 形式可能伴有叠加的脑炎性脱髓鞘(cAMN)。所有患者均携带 ABCD1 过氧化物酶体长链脂肪酸转运蛋白的功能丧失突变。即使在同一家庭中,导致基因型-表型相关性缺乏的因素在很大程度上仍不清楚。为了深入了解这一问题,我们比较了患有 cALD 的儿童和患有成人 cAMN 的患者形态完整的额白质区域的全基因组 DNA 甲基化谱,包括同年龄组的男性对照。我们在两种表型之间发现了一个共同的甲基化特征,包括:(i)在启动子区域具有 H3K27me3 标记的基因的 hypermethylation;(ii)在少突胶质细胞分化中起主要作用的基因的 hypermethylation,如 MBP、CNP、MOG 和 PLP1;(iii)免疫相关基因的 hypomethylation,如 IFITM1 和 CD59。此外,我们发现与 cAMN 相比,cALD 中与少突胶质细胞分化相关的基因的 CpG 中存在更多的 hypermethylation,并且在其启动子区域具有 H3K27me3 标记的基因也存在更多的 hypermethylation,这与转录和翻译变化有关。此外,使用惩罚逻辑回归模型,我们确定了 SPG20、UNC45A 和 COL9A3 的组合甲基化水平以及 ID4 和 MYRF 的组合表达水平是能够区分儿童和成人炎症表型的良好标志物。因此,我们提出假设,即表观遗传控制的改变转录程序可能导致 X-ALD 患者的少突胶质细胞分化受损和异常免疫激活。这些结果为疾病发病机制提供了启示,并揭示了有希望用于预后和表型分层的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4dfe/8028569/3b77510b159c/BPA-28-902-g008.jpg

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