Single Nucleotide Resolution 4sU Sequencing (SNU-Seq) reveals the transcriptional responsiveness of an epigenetically primed human genome
Umut Gerlevik, Philipp LorenziD, Anna R LamstaesiD, Harry FischliD, Shidong Xi, Aksel J. Saukko‐PaavolaiD, Struan C. Murray, Tom BrowniD, Alexander Welch, Charlotte L. GeorgeiD, Andrew AngeliD, André FurgeriD, Jane MelloriD
Abstract
Genomes are pervasively transcribed, leading to stable and unstable transcripts that influence 3-dimensional genome organisation and gene regulation. High sensitivity and nucleotide resolution are required to resolve mammalian nascent transcriptomes. Here, we exploit the sensitivity of 4-thio-uridine (4sU) metabolic pulse-labelling to develop two nucleotide-resolution methods: Single-Nucleotide resolution 4sU sequencing (SNU-Seq) and size-fractionated 4sU-Seq (sf4sU-Seq). sf4sU-Seq involves gel isolation of abundant 4sU-labelled promoter proximal nascent transcripts, enabling nucleotide resolution mapping of transcription start sites and promoter proximal pauses (PPPs) on the same transcript. SNU-Seq exploits 3 end RNA-Seq, using bacterial poly(A) polymerase (bPAP) to polyadenylate the 3 ends of nascent transcripts and create oligo(dT)-primed libraries. The artificial poly(A) tail marks the precise position of polymerase on a transcription unit. SNU-Seq read levels are similar at pre-mRNAs and enhancers genome-wide and read spikes in pre-mRNA outputs map pauses, PPPs and polyadenylation sites. SNU-Seq enables discovery of thousands of unannotated regions of divergent transcription and helps define hundreds of the more than 10,000 regions of primed non-transcribed acetylated open chromatin that induce divergent nascent transcripts within 0.5h of IFN-{gamma} treatment in Hep3B cells. Thus, combining chromatin analysis with SNU-Seq reveals the transcriptional responsiveness of an epigenetically primed human genome. HIGHLIGHTSO_LISNU-Seq maps nascent transcripts with bp resolution, high sensitivity and low cost C_LIO_LIsf4sU-Seq resolves TSS and PPP at the same gene, complementing SNU-Seq C_LIO_LI1000s of divergently transcribed enhancers resolved by SNU-Seq C_LIO_LIRapid IFN{gamma} dependent transcriptional induction from primed Hep3B epigenome C_LI GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=165 SRC="FIGDIR/small/452379v2_ufig1.gif" ALT="Figure 1"> View larger version (47K): org.highwire.dtl.DTLVardef@da6239org.highwire.dtl.DTLVardef@16692c6org.highwire.dtl.DTLVardef@12e30f7org.highwire.dtl.DTLVardef@190c98f_HPS_FORMAT_FIGEXP M_FIG C_FIG
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 2
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Synergising single-cell resolution and 4sU labelling boosts inference of transcriptional bursting
David M. Edwards, Philip Davies, Daniel Hebenstreit·Genome biologyPeer-reviewed·Jun 16, 2023
- Mapping and quantifying nascent transcript start sites using TT-TSS-seq
Eleanor Elgood Hunt, Claudia Vivori, … Folkert Jacobus van Werven·Genome ResearchPeer-reviewed·Mar 1, 2026
- Mapping the Location of Nucleosomes in Simian Virus 40 chromatin Using the New England Biolabs FS Library Prep Kit.
Barry I. Milavetz, Jacob Haugen, Kincaid Rowbotham·bioRxiv·Mar 27, 2020
- Single-cell nascent RNA sequencing using click-chemistry unveils coordinated transcription
Dig Bijay Mahat, Nathaniel D. Tippens, … Phillip A. Sharp·bioRxiv·Sep 15, 2023
- BuTT-Seq: a new method for facile profiling of transcription
Albert D. Yu, Michael Rosbash·bioRxiv·Mar 4, 2023
- Sequencing uracil in DNA at single-nucleotide resolution
L. Jiang, J. Yin, … Y.-H. Chen·bioRxiv·Jun 14, 2021