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Telomere maintenance through recruitment of internal genomic regions. | LitMetric

AI Article Synopsis

  • Cells that survive crises can become cancerous, often by reactivating telomerase, but some use a different method called alternative lengthening of telomeres (ALT).
  • Research in Caenorhabditis elegans shows that ALT survivors can escape sterility by duplicating certain genomic regions across telomeres, leading to genomic changes.
  • These regions, termed 'Template for ALT' (TALT), are characterized by telomere-like sequences and vary between different genetic backgrounds, suggesting a model for how ancestral duplications prepare these regions for telomere incorporation during ALT activation.

Article Abstract

Cells surviving crisis are often tumorigenic and their telomeres are commonly maintained through the reactivation of telomerase. However, surviving cells occasionally activate a recombination-based mechanism called alternative lengthening of telomeres (ALT). Here we establish stably maintained survivors in telomerase-deleted Caenorhabditis elegans that escape from sterility by activating ALT. ALT survivors trans-duplicate an internal genomic region, which is already cis-duplicated to chromosome ends, across the telomeres of all chromosomes. These 'Template for ALT' (TALT) regions consist of a block of genomic DNA flanked by telomere-like sequences, and are different between two genetic background. We establish a model that an ancestral duplication of a donor TALT region to a proximal telomere region forms a genomic reservoir ready to be incorporated into telomeres on ALT activation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4595603PMC
http://dx.doi.org/10.1038/ncomms9189DOI Listing

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