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Main Authors: Sun, Ke, Shen, Luemou, Wang, Junli, Zheng, Jiahao, Zhang, Xu, Luo, Fucheng, Chen, Kai, Song, Ning
Format: Artículo científico
Language:en
Published: Journal of genetics and genomics = Yi chuan xue bao 2026
Online Access:https://pubmed.ncbi.nlm.nih.gov/41866111/
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author Sun, Ke
Shen, Luemou
Wang, Junli
Zheng, Jiahao
Zhang, Xu
Luo, Fucheng
Chen, Kai
Song, Ning
author_facet Sun, Ke
Shen, Luemou
Wang, Junli
Zheng, Jiahao
Zhang, Xu
Luo, Fucheng
Chen, Kai
Song, Ning
Sun, Ke
Shen, Luemou
Wang, Junli
Zheng, Jiahao
Zhang, Xu
Luo, Fucheng
Chen, Kai
Song, Ning
collection PubMed - marine biology
contents Single-nucleotide transcription start sites profiling via Nascent Strand-Specific RNA sequencing uncovers IFN-γ-induced promoter dynamics. Sun, Ke Shen, Luemou Wang, Junli Zheng, Jiahao Zhang, Xu Luo, Fucheng Chen, Kai Song, Ning Transcriptional regulation is a highly dynamic process in which nascent RNAs provide the most immediate readout of transcriptional activity. Precise mapping of transcription start sites (TSSs) is therefore critical for understanding promoter architecture and gene regulation, yet remains technically challenging. Here, we introduce Nascent Strand-Specific RNA sequencing (NSS-seq), a robust and streamlined method for genome-wide profiling of the capped 5' ends of nascent RNAs. By directly capturing transcription initiation events, NSS-seq overcomes the temporal delay inherent to conventional RNA-seq and enables time-resolved interrogation of transcriptional dynamics. Applied to interferon-gamma (IFN-γ)-stimulation, NSS-seq uncovered previously unrecognized IFN-γ-responsive genes and transient transcription factor activation patterns underlying interferon-mediated tumor-suppressive functions. Together, NSS-seq provides a cost-effective and technically accessible platform for dissecting promoter-level regulatory dynamics during cellular responses.
format Artículo científico
id pubmed_41866111
institution PubMed
language en
publishDate 2026
publisher Journal of genetics and genomics = Yi chuan xue bao
record_format pubmed
spellingShingle Single-nucleotide transcription start sites profiling via Nascent Strand-Specific RNA sequencing uncovers IFN-γ-induced promoter dynamics.
Sun, Ke
Shen, Luemou
Wang, Junli
Zheng, Jiahao
Zhang, Xu
Luo, Fucheng
Chen, Kai
Song, Ning
Single-nucleotide transcription start sites profiling via Nascent Strand-Specific RNA sequencing uncovers IFN-γ-induced promoter dynamics. Sun, Ke Shen, Luemou Wang, Junli Zheng, Jiahao Zhang, Xu Luo, Fucheng Chen, Kai Song, Ning Transcriptional regulation is a highly dynamic process in which nascent RNAs provide the most immediate readout of transcriptional activity. Precise mapping of transcription start sites (TSSs) is therefore critical for understanding promoter architecture and gene regulation, yet remains technically challenging. Here, we introduce Nascent Strand-Specific RNA sequencing (NSS-seq), a robust and streamlined method for genome-wide profiling of the capped 5' ends of nascent RNAs. By directly capturing transcription initiation events, NSS-seq overcomes the temporal delay inherent to conventional RNA-seq and enables time-resolved interrogation of transcriptional dynamics. Applied to interferon-gamma (IFN-γ)-stimulation, NSS-seq uncovered previously unrecognized IFN-γ-responsive genes and transient transcription factor activation patterns underlying interferon-mediated tumor-suppressive functions. Together, NSS-seq provides a cost-effective and technically accessible platform for dissecting promoter-level regulatory dynamics during cellular responses.
title Single-nucleotide transcription start sites profiling via Nascent Strand-Specific RNA sequencing uncovers IFN-γ-induced promoter dynamics.
url https://pubmed.ncbi.nlm.nih.gov/41866111/