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HT Experiment :

Experiment Id  GSE226191 Name  Mbnl2 loss alters novel context processing and impairs object recognition memory
Experiment Type  RNA-Seq Study Type  WT vs. Mutant
Source  GEO Curation Date  2023-10-10
description  Myotonic dystrophy type I (DM1) patients demonstrate visuospatial dysfunction and impaired performance in tasks requiring recognition or memory of figures and objects. In DM1, CUG expansion RNAs inactivate the Muscleblind-like (MBNL) proteins. We show that constitutive Mbnl2 inactivation in DeltaE2/DeltaE2 mice, selectively impairs object recognition memory in the novel object recognition test. When exploring the context of a novel arena in which the objects are later encountered, the DeltaE2/DeltaE2 dorsal hippocampus responds with a lack of enrichment for learning and memory related pathways, mounting instead transcriptome alterations predicted to impair growth and neuron viability. In DeltaE2/DeltaE2 mice, saturation effects may prevent deployment of a functionally relevant transcriptome response during novel context exploration. Post-novel context exploration alterations in genes implicated in tauopathy and dementia are observed in the DeltaE2/DeltaE2 dorsal hippocampus. Thus MBNL2 inactivation in DM1 patients may alter novel context processing in the dorsal hippocampus and impair object recognition memory. Comparative gene expression profiling analysis of RNA-seq data for the dorsal hippocampus in 129sv/C57BL/6j Mbnl2 WT and KO mice
  • variables:
  • genotype,
  • bulk RNA-seq

1 Publications

Trail: HTExperiment

12 Samples

Trail: HTExperiment