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Related Concept Videos

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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
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Related Experiment Video

Updated: Jun 29, 2025

Mapping Genome-wide Accessible Chromatin in Primary Human T Lymphocytes by ATAC-Seq
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Exploring transient global transcriptional changes induced by ascorbic acid revealed via atKAS-seq profiling.

Xiangyue Liu1, Weizhi He1, Lulu Hu2

  • 1Cancer Institute, Fudan University Shanghai Cancer Center, Institutes of Biomedical Sciences, Shanghai Key Laboratory of Medical Epigenetics, International Co-Laboratory of Medical Epigenetics and Metabolism (Ministry of Science and Technology), Shanghai Medical College of Fudan University, Shanghai, 200032, China.

Functional & Integrative Genomics
|March 25, 2024
PubMed
Summary

A new method, adapter-tagged Kethoxal-assisted single-stranded DNA sequencing (atKAS-seq), efficiently maps DNA. This cost-effective technique analyzes transcription dynamics and enhancer activity, even with low sample input.

Keywords:
Adapter taggingAscorbic acidAtKAS-seqTranscription dynamics

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Area of Science:

  • Genomics
  • Molecular Biology
  • Epigenetics

Background:

  • Transcription creates dynamic single-stranded DNA (ssDNA) regions called transcription bubbles.
  • Kethoxal-assisted single-stranded DNA sequencing (KAS-seq) maps guanines in ssDNA genome-wide.
  • The original KAS-seq method has high costs and requires specific library kits.

Purpose of the Study:

  • To optimize KAS-seq for cost-efficiency and broader accessibility.
  • To introduce adapter-tagged KAS-seq (atKAS-seq) for streamlined ssDNA analysis.
  • To investigate epigenetic changes induced by ascorbic acid (ASC) using atKAS-seq.

Main Methods:

  • Developed adapter-tagged KAS-seq (atKAS-seq) with complementary strand synthesis and random N9 tagging.
  • Integrated sequencing adapters via a novel tagging strategy.
  • Applied atKAS-seq to study effects of short-term, high-dose ascorbic acid treatment.

Main Results:

  • atKAS-seq provides a cost-efficient, low-input alternative to original KAS-seq.
  • The method enables rapid and precise analysis of transcription dynamics.
  • atKAS-seq concurrently maps enhancer activities, revealing insights into ASC-induced epigenetic changes.

Conclusions:

  • atKAS-seq is a versatile tool for probing complex genomic regulatory mechanisms.
  • The optimized method enhances the study of transcription and enhancer function.
  • atKAS-seq facilitates accessible, high-resolution genomic analyses.