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GartnerAnton

Gartner, Anton
DNA Damage Response and Genetic Toxicology
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trt-1 is the Caenorhabditis elegans catalytic subunit of telomerase

Author(s)
Meier, BettinaClejan, IuvalLiu, YanLowden, MiaGartner, AntonHodgkin, JonathanAhmed, Shawn
Issued Date
2006-02
DOI
10.1371/journal.pgen.0020018
URI
https://scholarworks.unist.ac.kr/handle/201301/31014
Fulltext
https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.0020018
Citation
PLOS GENETICS, v.2, no.2, pp.187 - 197
Abstract
Mutants of trt-1, the Caenorhabditis elegans telomerase reverse transcriptase, reproduce normally for several generations but eventually become sterile as a consequence of telomere erosion and end-to-end chromosome fusions. Telomere erosion and uncapping do not cause an increase in apoptosis in the germlines of trt-1 mutants. Instead, late-generation trt-1 mutants display chromosome segregation defects that are likely to be the direct cause of sterility. trt-1 functions in the same telomere replication pathway as mrt-2, a component of the Rad9/Rad1/Hus1 (9-1-1) proliferating cell nuclear antigen - like sliding clamp. Thus, the 9 - 1 - 1 complex may be required for telomerase to act at chromosome ends in C. elegans. Although telomere erosion limits replicative life span in human somatic cells, neither trt-1 nor telomere shortening affects postmitotic aging in C. elegans. These findings illustrate effects of telomere dysfunction in C. elegans mutants lacking the catalytic subunit of telomerase, trt-1.
Publisher
PUBLIC LIBRARY SCIENCE
ISSN
1553-7404
Keyword
DNA-DAMAGEFUNCTIONAL MULTIMERIZATIONLENGTH MAINTENANCECHECKPOINT PROTEINTERMINAL DOMAINSFISSION YEASTLIFE-SPANRNAKUPATHWAY

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