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Originally published as MBC in Press, 10.1091/mbc.E06-10-0928 on March 1, 2007

Vol. 18, Issue 5, 1756-1767, May 2007

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Modulation of Cell Cycle–specific Gene Expressions at the Onset of S Phase Arrest Contributes to the Robust DNA Replication Checkpoint Response in Fission YeasFormula

Zhaoqing Chu*, Juntao Li{dagger}, Majid Eshaghi*, Xu Peng*, R. Krishna M. Karuturi{dagger}, and Jianhua Liu*,{ddagger}

*Biological Investigations and {dagger}Computational and Mathematical Biology, Genome Institute of Singapore, Singapore 118672; and {ddagger}Department of Biochemistry, National University of Singapore, Singapore 117595

Submitted October 18, 2006; Revised February 9, 2007; Accepted February 16, 2007
Monitoring Editor: Charles Boone

Fission yeast replication checkpoint kinases Rad3p and Cds1p are essential for maintaining cell viability after transient treatment with hydroxyurea (HU), an agent that blocks DNA replication. Although current studies have focused on the cyclin-dependent protein kinase Cdc2p that is regulated by these checkpoint kinases, other aspects of their functions at the onset of S phase arrest have not been fully understood. In this study, we use genome-wide DNA microarray analyses to show that HU-induced change of expression profiles in synchronized G2 cells occurs specifically at the onset of S phase arrest. Induction of many core environmental stress response genes and repression of ribosomal genes happen during S phase arrest. Significantly, peak expression level of the MluI-like cell cycle box (MCB)-cluster (G1) genes is maintained at the onset of S phase arrest in a Rad3p- and Cds1p-dependent manner. Expression level maintenance of the MCB-cluster is mediated through the accumulation of Rep2p, a putative transcriptional activator of the MBF complex. Conversely, the FKH-cluster (M) genes are repressed during the onset of S phase arrest in a Rad3p-dependent manner. Repression of the FKH-cluster genes is mediated through the decreased levels of one of the putative forkhead transcription factors, Sep1p, but not Fkh2p. Together, our results demonstrate that Rad3p and Cds1p modulate transcriptional response during the onset of S phase arrest.


This was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E06-10-0928) on March 1, 2007.

Formula The online version of this article contains supplemental material at MBC Online (http://www.molbiolcell.org).

Address correspondence to: Jianhua Liu (liujh{at}gis.a-star.edu.sg)




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