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Molecular and Cellular Biology, February 2007, p. 1017-1026, Vol. 27, No. 3
0270-7306/07/$08.00+0     doi:10.1128/MCB.01866-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Murine Pif1 Interacts with Telomerase and Is Dispensable for Telomere Function In Vivo{triangledown} ,{dagger}

Bryan E. Snow,1,2 Maria Mateyak,3,{ddagger} Jana Paderova,2,{ddagger} Andrew Wakeham,1,2 Caterina Iorio,1,2 Virginia Zakian,3 Jeremy Squire,2,4 and Lea Harrington1,2,4*

Campbell Family Institute for Breast Cancer Research, 620 University Avenue, Toronto, Ontario, Canada,1 Ontario Cancer Institute, 610 University Avenue, Toronto, Ontario, Canada,2 Princeton University, Lewis Thomas Laboratory, Princeton, New Jersey,3 Department of Medical Biophysics, University of Toronto, 610 University Avenue, Toronto, Ontario, Canada4

Received 2 October 2006/ Returned for modification 29 October 2006/ Accepted 10 November 2006

Pif1 is a 5'-to-3' DNA helicase critical to DNA replication and telomere length maintenance in the budding yeast Saccharomyces cerevisiae. ScPif1 is a negative regulator of telomeric repeat synthesis by telomerase, and recombinant ScPif1 promotes the dissociation of the telomerase RNA template from telomeric DNA in vitro. In order to dissect the role of mPif1 in mammals, we cloned and disrupted the mPif1 gene. In wild-type animals, mPif1 expression was detected only in embryonic and hematopoietic lineages. mPif1–/– mice were viable at expected frequencies, displayed no visible abnormalities, and showed no reproducible alteration in telomere length in two different null backgrounds, even after several generations. Spectral karyotyping of mPif1–/– fibroblasts and splenocytes revealed no significant change in chromosomal rearrangements. Furthermore, induction of apoptosis or DNA damage revealed no differences in cell viability compared to what was found for wild-type fibroblasts and splenocytes. Despite a novel association of mPif1 with telomerase, mPif1 did not affect the elongation activity of telomerase in vitro. Thus, in contrast to what occurs with ScPif1, murine telomere homeostasis or genetic stability does not depend on mPif1, perhaps due to fundamental differences in the regulation of telomerase and/or telomere length between mice and yeast or due to genetic redundancy with other DNA helicases.

* Corresponding author. Mailing address: Ontario Cancer Institute, Campbell Family Institute for Breast Cancer Research, 620 University Avenue, Room 706, Toronto M5G 2C1, Canada. Phone: (416) 946-2834. Fax: (416) 204-2277. E-mail: lea.harrington{at}oci.utoronto.ca.

{triangledown} Published ahead of print on 27 November 2006.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.

{ddagger} These authors contributed equally.

Molecular and Cellular Biology, February 2007, p. 1017-1026, Vol. 27, No. 3
0270-7306/07/$08.00+0     doi:10.1128/MCB.01866-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



This article has been cited by other articles:

  • Pinter, S. F., Aubert, S. D., Zakian, V. A. (2008). The Schizosaccharomyces pombe Pfh1p DNA Helicase Is Essential for the Maintenance of Nuclear and Mitochondrial DNA. Mol. Cell. Biol. 28: 6594-6608 [Abstract] [Full Text]  


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