Whole genome methylation sequencing in blood identifies extensive differential DNA methylation in late-onset dementia due to Alzheimer's disease

血液全基因组甲基化测序鉴定出阿尔茨海默病引起的晚发性痴呆中广泛的差异 DNA 甲基化

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作者:Coleman Breen, Ligia A Papale, Lindsay R Clark, Phillip E Bergmann, Andy Madrid, Sanjay Asthana, Sterling C Johnson, Sündüz Keleş, Reid S Alisch, Kirk J Hogan

Discussion

WGMS identifies differentially methylated CpGs in known and newly detected genes and enhancers in blood from persons with and without AD. Highlights: Whole genome DNA methylation levels were quantified in blood from persons with and without Alzheimer's disease (AD). Twenty-eight thousand thirty-eight differentially methylated positions (DMPs) were identified. Two thousand seven hundred seven genes comprise DMPs. Forty-eight of 75 independent genetic risk loci for AD have DMPs. One thousand five hundred sixty-eight blood-specific enhancers comprise DMPs, 173 of which interact with the promoters of 95 genes that are differentially expressed in blood from persons with and without AD.

Methods

We used whole genome methylation sequencing (WGMS) to quantify DNA methylation levels at 25,409,826 CpG loci in 281 blood samples from 108 AD and 173 cognitively unimpaired individuals.

Results

WGMS identified 28,038 DMPs throughout the human methylome, including 2707 differentially methylated genes (e.g., SORCS3, GABA, and PICALM) encoding proteins in biological pathways relevant to AD such as synaptic membrane, cation channel complex, and glutamatergic synapse. One hundred seventy-three differentially methylated blood-specific enhancers interact with the promoters of 95 genes that are differentially expressed in blood from persons with and without AD.

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