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Journal article

Nucleotide resolution 4-thiouridine sequencing by SNU-Seq and sf4sU-Seq reveals the transcriptional responsiveness of an epigenetically primed human genome

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 transcriptomes. Here, we exploit the sensitivity of 4-thiouridine (4sU) in 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 transcripts, enabling nucleotide resolution mapping of transcription start sites and promoter proximal pauses (PPPs) around +63 nucleotides on Pol II-transcribed loci. SNU-Seq maps the precise position of polymerases on transcription units, including paused Pol II at the PPP, validated using sf4sU-Seq, and enables the discovery of thousands of divergently transcribed intragenic and intergenic regions of open chromatin, many uncharacterised. Conversely and consistent with extensive epigenetic priming, hundreds of the >10,000 regions of acetylated open chromatin lacking detectable transcription using SNU-Seq, show IFNγ-dependent induction of divergent transcription, linked at selected loci to the formation of promoter-enhancer loops. At other primed regions, formation of promoter-enhancer loops is coincident with divergent transcription at the enhancer but precedes transcription of pre-mRNA from the promoter, supporting distinct priming mechanisms. Thus, 4sU-based methods, coupled to chromatin analysis, enable detailed characterisation of genome structure, transcription and responsiveness.
Publication status:
Accepted
Peer review status:
Peer reviewed

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Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
ORCID:
0000-0003-4288-6340
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
ORCID:
0000-0001-6548-3419
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author


More from this funder
Funder identifier:
https://ror.org/00k4n6c32
Grant:
860675
Programme:
Horizon 2020 Research and Innovation programme
More from this funder
Funder identifier:
https://ror.org/03wnrjx87
Grant:
UF120327
More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
WT089156MA
209897/Z/17/Z
091911
More from this funder
Funder identifier:
https://ror.org/012mzw131
Grant:
RPG-2016-405
More from this funder
Funder identifier:
https://ror.org/00cwqg982
Grant:
EP/F500394/1
BB/S009035/1
BB/N001184/1
BB/P00296X/1
BB/M011224/1
BB/Y005848/1
1757793


Publisher:
Oxford University Press
Journal:
Nucleic Acids Research More from this journal
Acceptance date:
2026-06-06
EISSN:
1362-4962
ISSN:
0305-1048


Language:
English
Pubs id:
2431061
Local pid:
pubs:2431061
Deposit date:
2026-06-08
ARK identifier:


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