How Shelterin Solves the Telomere End-Protection Problem
pmid: 21209389
How Shelterin Solves the Telomere End-Protection Problem
The symphony of the human genome concludes with a long Gregorian chant of TTAGGG repeats. This monotonous coda represents one of the most complex problems in chromosome biology: the question of how cells distinguish their natural chromosome ends from double-strand breaks elsewhere in the genome. McClintock's classic finding of chromosome breakage-fusion-bridge cycles, first reported by her at one of the early Cold Spring Harbor Laboratory Symposia (the ninth), served as a prelude to this question. The 75th Cold Spring Harbor Laboratory Symposium marks the completion of a series of mouse gene deletion experiments that revealed DNA-damage-response pathways that threaten chromosome ends and how the components of the telomeric shelterin complex prevent activation of these pathways.
- Rockefeller University United States
Recombination, Genetic, Base Sequence, DNA Repair, Tumor Suppressor Proteins, Molecular Sequence Data, Telomere-Binding Proteins, Cell Cycle Proteins, Ataxia Telangiectasia Mutated Proteins, Protein Serine-Threonine Kinases, Telomere, Models, Biological, DNA-Binding Proteins, Mice, Animals, Humans
Recombination, Genetic, Base Sequence, DNA Repair, Tumor Suppressor Proteins, Molecular Sequence Data, Telomere-Binding Proteins, Cell Cycle Proteins, Ataxia Telangiectasia Mutated Proteins, Protein Serine-Threonine Kinases, Telomere, Models, Biological, DNA-Binding Proteins, Mice, Animals, Humans
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