Abstract

Besides being a mediator of initiation of DNA replication, DNA polymerase α plays a key role in chromosome maintenance. Swi7H4, a novel temperature sensitive mutant of DNA polymerase α was shown to be defective in transcriptional silencing at the mating type centromere and telomere loci. It is also required for the establishment of chromatin state that can recruit the components of the heterochromatin machinery at these regions. Recently the role of DNA polymerase α in the S-phase alkylation damage response in S. pombe has also been studied. Here we investigate whether defects generated by swi7H4, a mutant allele of DNA polymerase α can activate a checkpoint response. We show that swi7H4 exhibit conditional synthetic lethality with chk1 null mutant and the double mutant of swi7H4 with chk1 deletion aggravate the chromosome segregation defects. More importantly swi7H4 mutant cells delay the mitotic progression at non permissive temperature that is mediated by checkpoint protein kinase Chk1. In addition we show that, in the swi7H4 mutant background, cells accumulate DNA damage at non permissive temperature activating the checkpoint kinase protein Chk1. Further, we observed synthetic lethality between swi7H4 and a number of genes involved in DNA repair pathway at semi permissive temperature. We summarize that defects in swi7H4 mutant results in DNA damage that delay mitosis in a Chk1 dependent manner that also require the damage repair pathway for proper recovery.

Highlights

  • Faithful chromosomal segregation is precisely monitored by the array of proteins involved in cell cycle events, like DNA replication, repair, mitosis and cytokinesis

  • The samples were collected at a 15 min interval and the number of cells having two nuclei was counted as an indication of cells entering into mitosis as described previously [24]

  • Swi7H4 exhibit conditional synthetic lethality with Chk1 null mutant swi7H4, a temperature sensitive mutant allele of DNA polymerase α is required for the establishment of silencing in fission yeast [12,13]

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Summary

Introduction

Faithful chromosomal segregation is precisely monitored by the array of proteins involved in cell cycle events, like DNA replication, repair, mitosis and cytokinesis. Swi7H4 mutant cells accumulate DNA damage at non permissive temperature and activate the checkpoint kinase protein Chk1. While wild type and chk1 delete cells did not exhibit any chromosome segregation defects, an approximately 10 fold increase in the frequency of aberrant mitosis in chk1 delete swi7H4 double mutant (10%) as compare to swi7H4 single mutant (1%) was observed after 6 hr at restrictive temperature (Fig 2A and 2B).

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