Journal
EMBO JOURNAL
Volume 31, Issue 8, Pages 2024-2033Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/emboj.2012.61
Keywords
ALT; C. elegans; stress; telomere maintenance
Categories
Funding
- Glenn Foundation
- EMBO
- Blasker Science and Technology Award
- Merieux Research Foundation
- Salk Institute Cancer Center Core [P30 CA009370-29]
- NIH [AG025837, GM087476]
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To counteract replication-dependent telomere shortening most eukaryotic cells rely on the telomerase pathway, which is crucial for the maintenance of proliferative potential of germ and stem cell populations of multicellular organisms. Likewise, cancer cells usually engage the telomerase pathway for telomere maintenance to gain immortality. However, in similar to 10% of human cancers telomeres are maintained through telomerase-independent alternative lengthening of telomeres (ALT) pathways. Here, we describe the generation and characterization of C. elegans survivors in a strain lacking the catalytic subunit of telomerase and the nematode telomere-binding protein CeOB2. These clonal strains, some of which have been propagated for > 180 generations, represent the first example of a multicellular organism with canonical telomeres that can survive without a functional telomerase pathway. The animals display the heterogeneous telomere length characteristic for ALT cells, contain single-stranded C-circles, a transcription profile pointing towards an adaptation to chronic stress and are therefore a unique and valuable tool to decipher the ALT mechanism. The EMBO Journal (2012) 31, 2024-2033. doi:10.1038/emboj.2012.61; Published online 16 March 2012 Subject Categories: genome stability & dynamics
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