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Mus musculus Transcriptome or Gene expression

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NIAID Data Ecosystem2026-05-17 收录
下载链接:
https://www.ncbi.nlm.nih.gov/sra/SRP097635
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TU-tagging is an intersectional method for covalently labeling newly transcribed RNAs within specific cell types. Cell type specificity is generated through targeted transgenic expression of the enzyme uracil phosphoribosyl transferase (UPRT); temporal specificity is generated through a pulse of the modified uracil analog 4-thiouracil (4TU). This technique has been applied in mouse using a Cre-dependent UPRT transgene, CA>GFPstop>HA-UPRT, to profile RNAs in endothelial cells, but it remained untested whether 4TU can cross the blood brain barrier (BBB) or whether this transgene can be used to purify neuronal RNAs. Here we crossed the CA>GFPstop>HA-UPRT transgenic mouse to a Sepw1-cre line to express UPRT in layer 2/3 of visual cortex or to an Nr5a1-cre line to express UPRT in layer 4 of visual cortex. We purified thiol-tagged mRNA from both genotypes at postnatal day 12, as well as from WT mice not expressing UPRT (background control). We found that a comparison of Sepw1-purified RNA to WT or Nr5a1-purified RNA allowed us to identify genes enriched in layer 2/3 of visual cortex. Here we show that Cre-dependent UPRT expression can be used to purify cell type specific mRNA from the intact mouse brain and provide the first evidence that 4TU can cross the blood brain barrier to label RNA in vivo.
创建时间:
2017-11-21
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