Summary information and primary citation
- PDB-id
- 6uso; SNAP-derived features in text and JSON formats;
DNAproDB
- Class
- nuclear protein, transferase-RNA-DNA
- Method
- X-ray (2.54 Å)
- Summary
- Telomerase reverse transcriptase prenucleotide binary complex, tert:DNA
- Reference
- Schaich MA, Sanford SL, Welfer GA, Johnson SA, Khoang TH, Opresko PL, Freudenthal BD (2020): "Mechanisms of nucleotide selection by telomerase." Elife, 9. doi: 10.7554/eLife.55438.
- Abstract
- Telomerase extends telomere sequences at chromosomal ends to protect genomic DNA. During this process it must select the correct nucleotide from a pool of nucleotides with various sugars and base pairing properties, which is critically important for the proper capping of telomeric sequences by shelterin. Unfortunately, how telomerase selects correct nucleotides is unknown. Here, we determined structures of Tribolium castaneum telomerase reverse transcriptase (TERT) throughout its catalytic cycle and mapped the active site residues responsible for nucleoside selection, metal coordination, triphosphate binding, and RNA template stabilization. We found that TERT inserts a mismatch or ribonucleotide ~1 in 10,000 and ~1 in 14,000 insertion events, respectively. At biological ribonucleotide concentrations, these rates translate to ~40 ribonucleotides inserted per 10 kilobases. Human telomerase assays determined a conserved tyrosine steric gate regulates ribonucleotide insertion into telomeres. Cumulatively, our work provides insight into how telomerase selects the proper nucleotide to maintain telomere integrity.