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RNA-Seq Mouse Brain Regions Expression Data Analysis: Focus on ApoE Functional Network

Vladimir N Babenko1, Dmitry A Smagin1, Natalia N Kudryavtseva1

  • 1Modeling Neuropathology Laboratory, Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences, Novosibirsk, Russia.

Journal of Integrative Bioinformatics
|September 14, 2017
PubMed
Summary
This summary is machine-generated.

Apolipoprotein E (ApoE) gene expression in the brain is linked to energy metabolism. Chronic stress significantly increases ApoE levels in the hypothalamus, suggesting a neuroendocrine stress response.

Keywords:
ApoEAppPomcRNA-Seq dataTomm40brain lipid metabolismbrain regionsdifferentially expressed genesgene expression profilehypothalamussocial stress mouse model

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Area of Science:

  • Neuroscience
  • Molecular Biology
  • Genetics

Background:

  • Apolipoprotein E (ApoE) expression is a specific marker for brain energy metabolism.
  • The ApoE genomic region, including Translocase of Outer Mitochondrial Membrane 40 kDa (TOMM40), is a neuroenergetic hotspot involved in mitochondrial metabolism.

Purpose of the Study:

  • To investigate the role of ApoE expression in the brain's response to chronic stress.
  • To identify alterations in gene expression within the ApoE locus under stressful conditions.

Main Methods:

  • Utilized RNA-Sequencing (RNA-Seq) data from a murine model of chronic stress.
  • Analyzed gene expression patterns in five distinct brain regions.
  • Performed correlation analysis between ApoE and proopiomelanocortin (Pomc) gene expression.

Main Results:

  • Observed significant positive expression coordination of seven neighboring genes in the ApoE locus across five brain regions under chronic stress.
  • Demonstrated a statistically significant increase in ApoE expression in the hypothalamus of chronically aggressive and defeated mice compared to controls.
  • Revealed a close association between ApoE and Pomc gene expression profiles in the hypothalamus.

Conclusions:

  • ApoE expression can drive alterations in neighboring gene expression under stressful loads.
  • Elevated ApoE expression in the hypothalamus under chronic stress conditions suggests a role in the neuroendocrine stress response.
  • The findings highlight the neuroenergetic significance of the ApoE locus in brain responses to stress.