| Literature DB >> 29887381 |
Sheel Shah1, Yodai Takei2, Wen Zhou2, Eric Lubeck3, Jina Yun2, Chee-Huat Linus Eng2, Noushin Koulena2, Christopher Cronin2, Christoph Karp2, Eric J Liaw4, Mina Amin5, Long Cai6.
Abstract
Visualization of the transcriptome and the nuclear organization in situ has been challenging for single-cell analysis. Here, we demonstrate a multiplexed single-molecule in situ method, intron seqFISH, that allows imaging of 10,421 genes at their nascent transcription active sites in single cells, followed by mRNA and lncRNA seqFISH and immunofluorescence. This nascent transcriptome-profiling method can identify different cell types and states with mouse embryonic stem cells and fibroblasts. The nascent sites of RNA synthesis tend to be localized on the surfaces of chromosome territories, and their organization in individual cells is highly variable. Surprisingly, the global nascent transcription oscillated asynchronously in individual cells with a period of 2 hr in mouse embryonic stem cells, as well as in fibroblasts. Together, spatial genomics of the nascent transcriptome by intron seqFISH reveals nuclear organizational principles and fast dynamics in single cells that are otherwise obscured.Entities:
Keywords: chromosome; intron; nascent transcriptome; oscillations; seqFISH; smFISH; transcription
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Year: 2018 PMID: 29887381 PMCID: PMC6046268 DOI: 10.1016/j.cell.2018.05.035
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582