Transcription shapes DNA replication initiation and termination in human cells

Yu Hung Chen, Sarah Keegan, Malik Kahli, Peter Tonzi, David Fenyö, Tony T. Huang, Duncan Smith

Research output: Contribution to journalArticle

Abstract

Although DNA replication is a fundamental aspect of biology, it is not known what determines where DNA replication starts and stops in the human genome. We directly identified and quantitatively compared sites of replication initiation and termination in untransformed human cells. We found that replication preferentially initiates at the transcription start site of genes occupied by high levels of RNA polymerase II, and terminates at their polyadenylation sites, thereby ensuring global co-directionality of transcription and replication, particularly at gene 5′ ends. During replication stress, replication initiation is stimulated downstream of genes and termination is redistributed to gene bodies; this globally reorients replication relative to transcription around gene 3′ ends. These data suggest that replication initiation and termination are coupled to transcription in human cells, and propose a model for the impact of replication stress on genome integrity.

Original languageEnglish (US)
Pages (from-to)67-77
Number of pages11
JournalNature Structural and Molecular Biology
Volume26
Issue number1
DOIs
StatePublished - Jan 1 2019

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DNA Replication
Genes
Polyadenylation
RNA Polymerase II
Transcription Initiation Site
Human Genome
Genome

ASJC Scopus subject areas

  • Structural Biology
  • Molecular Biology

Cite this

Transcription shapes DNA replication initiation and termination in human cells. / Chen, Yu Hung; Keegan, Sarah; Kahli, Malik; Tonzi, Peter; Fenyö, David; Huang, Tony T.; Smith, Duncan.

In: Nature Structural and Molecular Biology, Vol. 26, No. 1, 01.01.2019, p. 67-77.

Research output: Contribution to journalArticle

Chen, Yu Hung ; Keegan, Sarah ; Kahli, Malik ; Tonzi, Peter ; Fenyö, David ; Huang, Tony T. ; Smith, Duncan. / Transcription shapes DNA replication initiation and termination in human cells. In: Nature Structural and Molecular Biology. 2019 ; Vol. 26, No. 1. pp. 67-77.
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