학술논문

DNA methylation study of Huntington's disease and motor progression in patients and in animal models.
Document Type
article
Source
Nature communications. 11(1)
Subject
Animals
Animals
Genetically Modified
Sheep
Humans
Mice
Huntington Disease
Disease Models
Animal
Disease Progression
Recombinant Proteins
Severity of Illness Index
Registries
Longitudinal Studies
Follow-Up Studies
Prospective Studies
Cross-Sectional Studies
Behavior
Animal
DNA Methylation
Epigenesis
Genetic
CpG Islands
Mutation
Adolescent
Adult
Aged
Aged
80 and over
Middle Aged
Female
Male
Genome-Wide Association Study
Young Adult
Gene Knock-In Techniques
Genetic Loci
Huntingtin Protein
Global Burden of Disease
Genetically Modified
Disease Models
Animal
Behavior
Epigenesis
Genetic
and over
Language
Abstract
Although Huntington's disease (HD) is a well studied Mendelian genetic disorder, less is known about its associated epigenetic changes. Here, we characterize DNA methylation levels in six different tissues from 3 species: a mouse huntingtin (Htt) gene knock-in model, a transgenic HTT sheep model, and humans. Our epigenome-wide association study (EWAS) of human blood reveals that HD mutation status is significantly (p