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Series GSE64810 Query DataSets for GSE64810
Status Public on Dec 08, 2015
Title mRNA-Seq Expression profiling of human post-mortem BA9 brain tissue for Huntington's Disease and neurologically normal individuals
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Huntington’s Disease (HD) is a devastating neurodegenerative disorder that is caused by an expanded CAG trinucleotide repeat in the Huntingtin (HTT) gene. Transcriptional dysregulation in the human HD brain has been documented but is incompletely understood. Here we present a genome-wide analysis of mRNA expression in human prefrontal cortex from 20 HD and 49 neuropathologically normal controls using next generation high-throughput sequencing. Surprisingly, 19% (5,480) of the 28,087 confidently detected genes are differentially expressed (FDR<0.05) and are predominantly up-regulated. A novel hypothesis-free geneset enrichment method that dissects large gene lists into functionally and transcriptionally related groups discovers that the differentially expressed genes are enriched for immune response, neuroinflammation, and developmental genes. Markers for all major brain cell types are observed, suggesting that HD invokes a systemic response in the brain area studied. Unexpectedly, the most strongly differentially expressed genes are a homeotic gene set (represented by Hox and other homeobox genes), that are almost exclusively expressed in HD, a profile not widely implicated in HD pathogenesis. The significance of transcriptional changes of developmental processes in the HD brain is poorly understood and warrants further investigation. The role of inflammation and the significance of non-neuronal involvement in HD pathogenesis suggest anti-inflammatory therapeutics may offer important opportunities in treating HD.
 
Overall design 20 Huntington's Disease and 49 neurologically normal control samples from post-mortem human subjects
 
Contributor(s) Labadorf A, Myers R, Hoss A
Citation(s) 26636579, 29375298, 31619230
Submission date Jan 09, 2015
Last update date Oct 29, 2019
Contact name Adam Labadorf
E-mail(s) labadorf@bu.edu
Organization name Boston University Medical School
Department Neurology
Street address 72 East Concord Street E301
City Boston
State/province MA
ZIP/Postal code 02118
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (69)
GSM1580869 C_0002
GSM1580870 C_0003
GSM1580871 C_0004
Relations
BioProject PRJNA271929
SRA SRP051844

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE64810_mlhd_DESeq2_diffexp_DESeq2_outlier_trimmed_adjust.txt.gz 2.1 Mb (ftp)(http) TXT
GSE64810_mlhd_DESeq2_norm_counts_adjust.txt.gz 12.1 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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