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Article

The Chinese Hamster Dihydrofolate Reductase Replication Origin Decision Point Follows Activation of Transcription and Suppresses Initiation of Replication within Transcription Units

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Pages 1051-1062 | Received 07 Sep 2005, Accepted 15 Nov 2005, Published online: 27 Mar 2023
 

Abstract

Chinese hamster ovary (CHO) cells select specific replication origin sites within the dihydrofolate reductase (DHFR) locus at a discrete point during G1 phase, the origin decision point (ODP). Origin selection is sensitive to transcription but not protein synthesis inhibitors, implicating a pretranslational role for transcription in origin specification. We have constructed a DNA array covering 121 kb surrounding the DHFR locus, to comprehensively investigate replication initiation and transcription in this region. When nuclei isolated within the first 3 h of G1 phase were stimulated to initiate replication in Xenopus egg extracts, replication initiated without any detectable preference for specific sites. At the ODP, initiation became suppressed from within the Msh3, DHFR, and 2BE2121 transcription units. Active transcription was mostly confined to these transcription units, and inhibition of transcription by alpha-amanitin resulted in the initiation of replication within transcription units, indicating that transcription is necessary to limit initiation events to the intergenic region. However, the resumption of DHFR transcription after mitosis took place prior to the ODP and so is not on its own sufficient to suppress initiation of replication. Together, these results demonstrate a remarkable flexibility in sequence selection for initiating replication and implicate transcription as one important component of origin specification at the ODP.

We thank J. Hamlin and L. Chasin for providing cosmids and plasmids with which to complete our sequencing analysis; M. Hawkins, J. Merrit, and A. Leskovar for technical assistance; Paul Bertone, L. Chasin, and J. Lis for helpful discussions; and J. Huberman for critical review of the manuscript.

This work was supported by NIH grant GM-57233 to D.M.G. T.S. was supported by a fellowship from the New York State DOH Breast Cancer Initiative.

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