Genetic Control of Telomere Integrity in Schizosaccharomyces pombe: rad3⁺ and tel1⁺ Are Parts of Two Regulatory Networks Independent of the Downstream Protein Kinases chk1⁺ and cds1⁺

Corresponding author: Akira Matsuura, Department of Life Science, Graduate School of Bioscience and Biotechnology, Tokyo Institute of Technology, Nagatsuta, Midori-ku, Yokohama 226-8501, Japan., amatsuur{at}bio.titech.ac.jp (E-mail)

Communicating editor: G. R. SMITH

The Schizosaccharomyces pombe checkpoint gene named rad3⁺ encodes an ATM-homologous protein kinase that shares a highly conserved motif with proteins involved in DNA metabolism. Previous studies have shown that Rad3 fulfills its function via the regulation of the Chk1 and Cds1 protein kinases. Here we describe a novel role for Rad3 in the control of telomere integrity. Mutations in the rad3⁺ gene alleviated telomeric silencing and produced shortened lengths in the telomere repeat tracts. Genetic analysis revealed that the other checkpoint rad mutations rad1, rad17, and rad26 belong to the same phenotypic class with rad3 with regard to control of the telomere length. Of these mutations, rad3 and rad26 have a drastic effect on telomere shortening. tel1⁺, another ATM homologue in S. pombe, carries out its telomere maintenance function in parallel with the checkpoint rad genes. Furthermore, either a single or double disruption of cds1⁺ and chk1⁺ caused no obvious changes in the telomeric DNA structure. Our results demonstrate a novel role of the S. pombe ATM homologues that is independent of chk1⁺ and cds1⁺.

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