Literature DB >> 27077668

Combining Double Fluorescence In Situ Hybridization with Immunolabelling for Detection of the Expression of Three Genes in Mouse Brain Sections.

Sarah Jolly1, Alexander Fudge1, Nigel Pringle1, William D Richardson2, Huiliang Li3.   

Abstract

Detection of gene expression in different types of brain cells e.g., neurons, astrocytes, oligodendrocytes, oligodendrocyte precursors and microglia, can be hampered by the lack of specific primary or secondary antibodies for immunostaining. Here we describe a protocol to detect the expression of three different genes in the same brain section using double fluorescence in situ hybridization with two gene-specific probes followed by immunostaining with an antibody of high specificity directed against the protein encoded by a third gene. The Aspartoacyclase (ASPA) gene, mutations of which can lead to a rare human white matter disease - Canavan disease - is thought to be expressed in oligodendrocytes and microglia but not in astrocytes and neurons. However, the precise expression pattern of ASPA in the brain has yet to be established. This protocol has allowed us to determine that ASPA is expressed in a subset of mature oligodendrocytes and it can be generally applied to a wide range of gene expression pattern studies.

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Year:  2016        PMID: 27077668      PMCID: PMC4841319          DOI: 10.3791/53976

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  17 in total

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Authors:  Christian S Lobsiger; Don W Cleveland
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Authors:  Batool F Kirmani; David M Jacobowitz; Abraham T Kallarakal; M A A Namboodiri
Journal:  Brain Res Mol Brain Res       Date:  2002-11-15

3.  An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex.

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4.  Developmental and regional distribution of aspartoacylase in rat brain tissue.

Authors:  K K Bhakoo; T J Craig; P Styles
Journal:  J Neurochem       Date:  2001-10       Impact factor: 5.372

Review 5.  N-acetylaspartate in the vertebrate brain: metabolism and function.

Authors:  Morris H Baslow
Journal:  Neurochem Res       Date:  2003-06       Impact factor: 3.996

6.  Biochemical diagnosis of Canavan disease.

Authors:  G Bartalini; M Margollicci; P Balestri; M A Farnetani; M Cioni; A Fois
Journal:  Childs Nerv Syst       Date:  1992-12       Impact factor: 1.475

7.  Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease.

Authors:  R Kaul; G P Gao; K Balamurugan; R Matalon
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

8.  Immunohistochemical localization of aspartoacylase in the rat central nervous system.

Authors:  Chikkathur N Madhavarao; John R Moffett; Roger A Moore; Ronald E Viola; M A Aryan Namboodiri; David M Jacobowitz
Journal:  J Comp Neurol       Date:  2004-05-03       Impact factor: 3.215

9.  Identification and distribution of aspartoacylase in the postnatal rat brain.

Authors:  Matthias Klugmann; C Wymond Symes; Bettina K Klaussner; Claudia B Leichtlein; Tadao Serikawa; Deborah Young; Matthew J During
Journal:  Neuroreport       Date:  2003-10-06       Impact factor: 1.837

Review 10.  Canavan disease: clinical features and recent advances in research.

Authors:  Hideki Hoshino; Masaya Kubota
Journal:  Pediatr Int       Date:  2014-08       Impact factor: 1.524

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5.  G protein-coupled receptor 37-like 1 modulates astrocyte glutamate transporters and neuronal NMDA receptors and is neuroprotective in ischemia.

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6.  Signalling through AMPA receptors on oligodendrocyte precursors promotes myelination by enhancing oligodendrocyte survival.

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8.  Increasing Aspartoacylase in the Central Amygdala: The Common Mechanism of Gastroprotective Effects of Monoamine-Based Antidepressants Against Stress.

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9.  Rapid production of new oligodendrocytes is required in the earliest stages of motor-skill learning.

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Journal:  Nat Neurosci       Date:  2016-07-25       Impact factor: 24.884

  9 in total

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