Saccharomyces Rrm3p, a 5′ to 3′ DNA helicase that promotes replication fork progression through telomeric and subtelomeric DNA (original) (raw)
- Andreas S. Ivessa1,
- Jin-Qiu Zhou1,2,
- Vince P. Schulz,
- Ellen K. Monson, and
- Virginia A. Zakian3
- Department of Molecular Biology, Princeton University, Princeton, New Jersey 08544-1014, USA
Abstract
In wild-type Saccharomyces cerevisiae, replication forks slowed during their passage through telomeric C1–3A/TG1–3 tracts. This slowing was greatly exacerbated in the absence of RRM3, shown here to encode a 5′ to 3′ DNA helicase. Rrm3p-dependent fork progression was seen at a modified Chromosome VII-L telomere, at the natural X-bearing Chromosome III-L telomere, and at Y‘-bearing telomeres. Loss of Rrm3p also resulted in replication fork pausing at specific sites in subtelomeric DNA, such as at inactive replication origins, and at internal tracts of C1–3A/TG1–3 DNA. The ATPase/helicase activity of Rrm3p was required for its role in telomeric and subtelomeric DNA replication. Because Rrm3p was telomere-associated in vivo, it likely has a direct role in telomere replication.
Footnotes
↵1 These authors contributed equally to this work.
↵2 Present address: Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, P.R. China.
↵3 Corresponding author.
E-MAIL vzakian{at}molbio.princeton.edu; FAX (609) 258-1701.
Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.982902.
- Received February 7, 2002.
- Accepted April 10, 2002.
Cold Spring Harbor Laboratory Press