<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE124726" accession="SRP176459">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP176459</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA513334</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE124726</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>ASO-mediated RNA Suppression through Targeted Epigenetic Reprogramming of the Hdac2 Gene</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>We elicited ASO-mediated knockdown of mRNAs in the nervous system by targeting the memory-repressor gene Histone deacetylase 2 (Hdac2) in vitro and in vivo. We observed that an Hdac2-targeted ASO not only triggered a reduction in mRNA levels, but also a direct transcriptional suppression of the Hdac2 gene in neurons in vitro. In further in vivo studies, we observed that a single dose of the Hdac2-targeted ASO delivered by intracerebroventricular injection into the central nervous system (CNS) achieved steady-state diminution of Hdac2 mRNA levels that lasted more than 6 months in vivo. Knockdown of this factor resulted in memory enhancement. ASO administration also caused a prolonged alteration of steady-state levels of a set of known memory-associated mRNAs and triggered secondary changes in the epigenome at sites outside of the primary target gene. Overall design: 3 scrambled ASO and 3 HDAC2 ASO mice were sacrificed and at 9 timepoints (3d, 2w, 4w, 8w, 16w, 32w, 40w, 48w, 52w) after ASO injection. Cortex, hippocampus and cerebellum were analyzed for total RNA expression. expression.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE124726</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>32160709</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
