Abstract
Mammalian telomeres end in single-stranded, G-rich 3′ overhangs resulting from both the "end-replication problem" (the inability of DNA polymerase to replicate the very end of the telomeres) and postreplication processing. Telomeric G-rich overhangs are precisely defined in ciliates; the length and the terminal nucleotides are fixed. Human telomeres have very long overhangs that are heterogeneous in size (35-600 nt), indicating that their processing must differ in some respects from model organisms. We developed telomere-end ligation protocols that allowed us to identify the terminal nucleotides of both the C-rich and the G-rich telomere strands. Up to ∼80% of the C-rich strands terminate in CCAATC-5′, suggesting that after replication a nuclease with high specificity or constrained action acts on the C strand. In contrast, the G-terminal nucleotide was less precise than Tetrahymena and Euplotes but still had a bias that changed as a function of telomerase expression. Copyright ©2005 by Elsevier Inc.
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CITATION STYLE
Sfeir, A. J., Chai, W., Shay, J. W., & Wright, W. E. (2005). Telomere-end processing: The terminal nucleotidesof human chromosomes. Molecular Cell, 18(1), 131–138. https://doi.org/10.1016/j.molcel.2005.02.035
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