2014The FASEB JournalRequires access

Identifying transcriptional changes in an oligodendrocyte‐specific conditional knockout mouse (934.6)

Taylor Stefanik, Gang Yu, Daniel R. Dries

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Abstract

gamma‐secretase is a proteolytic complex involved in development and implicated in the etiology of Alzheimer’s disease. We recently developed a conditional knockout mouse in which gamma‐secretase was specifically deleted from oligodendrocytes, the myelinating cells of the brain. The conditional knockout mouse had a profound neurological phenotype, including hyperactivity and decreased prepulse inhibition. Here, we use RNA‐seq to compare the transcriptional profiles of conditional knockout and control mice in an effort to identify a set of candidate genes that may explain the complex neurological phenotype of our conditional knockout mouse. Grant Funding Source : Supported by National Institute of Neurological Disorders and Stroke grant 1R01NS079796

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What this paper is about

gamma‐secretase is a proteolytic complex involved in development and implicated in the etiology of Alzheimer’s disease. We recently developed a conditional knockout mouse in which gamma‐secretase was specifically deleted from oligodendrocytes, the myelinating cells of the brain. The conditional knockout mouse had a profound neurological phenotype, including hyperactivity and decreased prepulse inhibition. Here, we use RNA‐seq to compare the transcriptional profiles of conditional knockout and control mice in an effort to identify a set of candidate genes that may explain the complex neurological phenotype of our conditional knockout mouse. Grant Funding Source : Supported by National Institute of Neurological Disorders and Stroke grant 1R01NS079796

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Available abstract

gamma‐secretase is a proteolytic complex involved in development and implicated in the etiology of Alzheimer’s disease. We recently developed a conditional knockout mouse in which gamma‐secretase was specifically deleted from oligodendrocytes, the myelinating cells of the brain. The conditional knockout mouse had a profound neurological phenotype, including hyperactivity and decreased prepulse inhibition. Here, we use RNA‐seq to compare the transcriptional profiles of conditional knockout and control mice in an effort to identify a set of candidate genes that may explain the complex neurological phenotype of our conditional knockout mouse. Grant Funding Source : Supported by National Institute of Neurological Disorders and Stroke grant 1R01NS079796

Key concepts: Conditional gene knockout, Knockout mouse, Phenotype, Prepulse inhibition, Neuroscience, Gene knockout, Biology, Gene

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