NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE255987 Query DataSets for GSE255987
Status Public on May 03, 2024
Title Brain-wide AAV-mediated silencing of prion protein by a compact epigenetic editor
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Prion disease is caused by misfolding of the prion protein (PrP) into pathogenic self-propagating conformations, leading to rapid onset dementia and death. However, elimination of endogenous PrP can halt prion disease progression. Here, we describe CHARM, a compact, enzyme-free epigenetic editor capable of silencing transcription through programmable targeted DNA methylation. Using a histone H3 tail-Dnmt3l fusion, CHARM recruits and activates the endogenous DNA methyltransferases, thereby reducing transgene size and bystander effects. When delivered to the mouse brain by an adeno-associated viral (AAV) vector, PRNP-targeted CHARM ablates PrP expression across the brain. We temporally limit editor expression by implementing a kinetically-tuned self-silencing approach. CHARM represents a broadly applicable strategy to programmably prevent expression of pathogenic proteins, including those implicated in other neurodegenerative diseases.
 
Overall design Neuro-2a cells were transduced with ZFcharm Kv1 and CRISPRcharm Kv1 lentiviral constructs. CISPRcharm Kv1 was introduced into cells already expressing either a non-targeting sgRNA or a sgRNA targeting Prnp. An empty lentiviral vector was used as a no-editor control. Each transduction was done in triplicate. Cells were dislodged from 6-well plates using Trizol and total RNA was extracted using the Direct-zol RNA Miniprep Kit (Zymo, R2051). Libraries were prepared using the KAPA RNA HyperPrep Kit with RiboErase (HMR) (Roche, KK8560) and sequenced as 50 bp single-end reads on a NovaSeq 6000 (Illumina). Raw sequencing reads were aligned to the mouse genome (mm39) using STAR 2.7.1a and quantified using featureCounts. Differential expression analysis was carried out using DESeq2.
 
Contributor(s) Bertozzi T, Neumann E, Weissman J
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Feb 16, 2024
Last update date May 03, 2024
Contact name Tessa Bertozzi
Organization name Whitehead Institute
Lab Weissman Lab
Street address 455 Main St
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platforms (1)
GPL24247 Illumina NovaSeq 6000 (Mus musculus)
Samples (15)
GSM8083828 Empty_vector_rep1
GSM8083829 Empty_vector_rep2
GSM8083830 Empty_vector_rep3
Relations
BioProject PRJNA1077350

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
GSE255987_raw_counts.txt.gz 4.4 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap