A genomic integration method to visualize localization of endogenous mRNAs in living yeast
- PMID: 17417645
- DOI: 10.1038/nmeth1040
A genomic integration method to visualize localization of endogenous mRNAs in living yeast
Abstract
mRNA localization may be an important determinant for protein localization. We describe a simple PCR-based genomic-tagging strategy (m-TAG) that uses homologous recombination to insert binding sites for the RNA-binding MS2 coat protein (MS2-CP) between the coding region and 3' untranslated region (UTR) of any yeast gene. Upon coexpression of MS2-CP fused with GFP, we demonstrate the localization of endogenous mRNAs (ASH1, SRO7, PEX3 and OXA1) in living yeast (Saccharomyces cerevisiae).
Comment in
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Splitting or stacking fluorescent proteins to visualize mRNA in living cells.Nat Methods. 2007 May;4(5):391-2. doi: 10.1038/nmeth0507-391. Nat Methods. 2007. PMID: 17464293 No abstract available.
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