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Chromosoma. 2016 Mar;125(1):65-73. doi: 10.1007/s00412-015-0528-7. Epub 2015 Jul 11.

Telomerase lost?

Author information

1
Laboratory of Genome Integrity and Structural Biology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
2
Integrative Bioinformatics, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.
3
Institute of Entomology, Biology Centre AS CR, Ceske Budejovice, Czech Republic. Radmila.Frydrychova@hotmail.com.

Abstract

Telomerase and telomerase-generated telomeric DNA sequences are widespread throughout eukaryotes, yet they are not universal. Neither telomerase nor the simple DNA repeats associated with telomerase have been found in some plant and animal species. Telomerase was likely lost from Diptera before the divergence of Diptera and Siphonaptera, some 260 million years ago. Even so, Diptera is one of the most successful animal orders, making up 11% of known animal species. In addition, many species of Coleoptera and Hemiptera seem to lack canonical telomeric repeats at their chromosome ends. These and other insects that appear to lack canonical terminal repeat sequences account for another 10-15% of animal species. Conversely, the silk moth Bombyx mori maintains canonical telomeric sequences at its chromosome ends but seems to lack a functional telomerase. We speculate that a telomere-specific capping complex that recognizes the telomeric repeats and protects chromosome ends is the determining factor in maintaining canonical telomeric sequences and that telomerase is an early and efficacious mechanism for satisfying the needs of capping complex. There are alternate mechanisms for maintaining chromosome ends that do not depend on telomerase, such as recombination found in some human cancer cells and yeast mutants. These mechanisms may maintain the canonical telomeric repeats or allow the terminal sequence to evolve when specificity of the capping complex for terminal repeat sequences is weak.

PMID:
26162505
PMCID:
PMC6512322
DOI:
10.1007/s00412-015-0528-7
[Indexed for MEDLINE]
Free PMC Article

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