Abstract
BackgroundEukaryotic DNA replication follows a specific temporal program, with some genomic regions consistently replicating earlier than others, yet what determines this program is largely unknown. Highly transcribed regions have been observed to replicate in early S-phase in all plant and animal species studied to date, but this relationship is thought to be absent from both budding yeast and fission yeast. No association between cell-cycle regulated transcription and replication timing has been reported for any species.ResultsHere I show that in budding yeast, fission yeast, and human, the genes most highly transcribed during S-phase replicate early, whereas those repressed in S-phase replicate late. Transcription during other cell-cycle phases shows either the opposite correlation with replication timing, or no relation. The relationship is strongest near late-firing origins of replication, which is not consistent with a previously proposed model—that replication timing may affect transcription—and instead suggests a potential mechanism involving the recruitment of limiting replication initiation factors during S-phase.ConclusionsThese results suggest that S-phase transcription may be an important determinant of DNA replication timing across eukaryotes, which may explain the well-established association between transcription and replication timing.
Highlights
Eukaryotic DNA replication follows a specific temporal program, with some genomic regions consistently replicating earlier than others, yet what determines this program is largely unknown
Because DNA replication is confined to a specific period during the cell cycle, I reasoned that the relationship between time of replication (Trep) and transcription may depend on when in the cell cycle transcription is occurring
I compared the expression levels of these cell cycle-regulated genes measured in synchronized cells [27,28] with the Trep for each gene to determine if any relationship exists
Summary
Eukaryotic DNA replication follows a specific temporal program, with some genomic regions consistently replicating earlier than others, yet what determines this program is largely unknown. The two major models [8,11], not mutually exclusive, are that 1) the euchromatic chromatin structure is more permissive both to transcription and to DNA replication initiation, or 2) Trep itself affects chromatin structure and transcription as a result of changes in the nuclear milieu during S-phase The former is most directly supported by experiments altering ORI firing time via manipulation of histone modifications [8,9,10,18,22,23,24], whereas the latter is supported by differences in chromatin and transcription of DNA templates injected into cells during either early or late S-phase [8,9,25,26]
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