Telomeres are essential for the maintenance of chromosome stability. In the absence of telomere function, chromosome ends fuse and progressive genomic rearrangements occur. In most eukaryotes, telomeres consist of tandem copies of simple sequences repeats. These telomere repeats are synthesized de novo onto chromosomes ends by the enzyme telomerase. Telomerase is a specialized DNA polymerase first identified in Tetrahymena. The enzyme contains an essential RNA component that provides the template for telomere repeat synthesis. Since its initial identification, telomerase activity and the RNA components have been characterized from a variety of eukaryotes. In humans, telomerase is activated during tumor growth and evidence suggests it may be a good target for cancer chemotherapy. Recently, telomerase protein components have been identified from Tetrahymena, Euplotes yeasts, and human cells. Although some of the protein components are conserved across species, it appears that not all of the telomerase components will be conserved. To take advantage of the well characterized reaction mechanism and the known structure of the RNA component, we are continuing to analyze function of the Tetrahymena telomerase enzyme. We will use the RNA component to probe the structure and function of the telomerase RNP. The protein components of telomerase will be further characterized and we will test their function in vitro and in vivo. Finally, we will take advantage of the unique biology of Tetrahymena to identify new components that are important in telomere maintenance.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM043080-13
Application #
6476508
Study Section
Molecular Cytology Study Section (CTY)
Program Officer
Ikeda, Richard A
Project Start
1989-12-01
Project End
2003-04-30
Budget Start
2001-12-01
Budget End
2003-04-30
Support Year
13
Fiscal Year
2002
Total Cost
$379,765
Indirect Cost
Name
Johns Hopkins University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Kaizer, Hannah; Connelly, Carla J; Bettridge, Kelsey et al. (2015) Regulation of Telomere Length Requires a Conserved N-Terminal Domain of Rif2 in Saccharomyces cerevisiae. Genetics 201:573-86
Ma, Yunmei; Greider, Carol W (2009) Kinase-independent functions of TEL1 in telomere maintenance. Mol Cell Biol 29:5193-202
Frank, Christopher J; Hyde, Molly; Greider, Carol W (2006) Regulation of telomere elongation by the cyclin-dependent kinase CDK1. Mol Cell 24:423-32
IJpma, Arne S; Greider, Carol W (2003) Short telomeres induce a DNA damage response in Saccharomyces cerevisiae. Mol Biol Cell 14:987-1001
Hackett, Jennifer A; Greider, Carol W (2003) End resection initiates genomic instability in the absence of telomerase. Mol Cell Biol 23:8450-61
Hackett, Jennifer A; Greider, Carol W (2002) Balancing instability: dual roles for telomerase and telomere dysfunction in tumorigenesis. Oncogene 21:619-26
Chen, Q; Ijpma, A; Greider, C W (2001) Two survivor pathways that allow growth in the absence of telomerase are generated by distinct telomere recombination events. Mol Cell Biol 21:1819-27
Mason, D X; Autexier, C; Greider, C W (2001) Tetrahymena proteins p80 and p95 are not core telomerase components. Proc Natl Acad Sci U S A 98:12368-73
Hackett, J A; Feldser, D M; Greider, C W (2001) Telomere dysfunction increases mutation rate and genomic instability. Cell 106:275-86
Kass-Eisler, A; Greider, C W (2000) Recombination in telomere-length maintenance. Trends Biochem Sci 25:200-4

Showing the most recent 10 out of 23 publications