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Rapid Molecular Profiling of Defined Cell Types Using Viral TRAP
Author(s) -
Alexander R. Nectow,
Maria V. Moya,
Mats I. Ekstrand,
Awni Mousa,
Kelly L. McGuire,
Caroline E. Sferrazza,
Bianca C. Field,
Gabrielle S. Rabinowitz,
Kirsty Sawicka,
Yupu Liang,
Jeffrey M. Friedman,
Nathaniel Heintz,
Eric F. Schmidt
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.03.048
Subject(s) - biology , cell type , cre recombinase , ribosome profiling , computational biology , gene expression profiling , adeno associated virus , cell , virus , gene , microbiology and biotechnology , gene expression , translation (biology) , transgene , virology , messenger rna , genetics , genetically modified mouse , recombinant dna , vector (molecular biology)
Translational profiling methodologies enable the systematic characterization of cell types in complex tissues, such as the mammalian brain, where neuronal isolation is exceptionally difficult. Here, we report a versatile strategy for profiling CNS cell types in a spatiotemporally restricted fashion by engineering a Cre-dependent adeno-associated virus expressing an EGFP-tagged ribosomal protein (AAV-FLEX-EGFPL10a) to access translating mRNAs by translating ribosome affinity purification (TRAP). We demonstrate the utility of this AAV to target a variety of genetically and anatomically defined neural populations expressing Cre recombinase and illustrate the ability of this viral TRAP (vTRAP) approach to recapitulate the molecular profiles obtained by bacTRAP in corticothalamic neurons across multiple serotypes. Furthermore, spatially restricting adeno-associated virus (AAV) injections enabled the elucidation of regional differences in gene expression within this cell type. Altogether, these results establish the broad applicability of the vTRAP strategy for the molecular dissection of any CNS or peripheral cell type that can be engineered to express Cre.

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