Structure of Tetrahymena telomerase reveals previously unknown subunits, functions, and interactions

Science. 2015 Oct 30;350(6260):aab4070. doi: 10.1126/science.aab4070. Epub 2015 Oct 15.

Abstract

Telomerase helps maintain telomeres by processive synthesis of telomere repeat DNA at their 3'-ends, using an integral telomerase RNA (TER) and telomerase reverse transcriptase (TERT). We report the cryo-electron microscopy structure of Tetrahymena telomerase at ~9 angstrom resolution. In addition to seven known holoenzyme proteins, we identify two additional proteins that form a complex (TEB) with single-stranded telomere DNA-binding protein Teb1, paralogous to heterotrimeric replication protein A (RPA). The p75-p45-p19 subcomplex is identified as another RPA-related complex, CST (CTC1-STN1-TEN1). This study reveals the paths of TER in the TERT-TER-p65 catalytic core and single-stranded DNA exit; extensive subunit interactions of the TERT essential N-terminal domain, p50, and TEB; and other subunit identities and structures, including p19 and p45C crystal structures. Our findings provide structural and mechanistic insights into telomerase holoenzyme function.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Catalytic Domain
  • Cryoelectron Microscopy
  • Crystallography, X-Ray
  • DNA, Single-Stranded / chemistry
  • Holoenzymes / chemistry
  • Protein Binding
  • Protein Conformation
  • Protein Subunits / chemistry
  • RNA / chemistry*
  • Replication Protein A / chemistry
  • Telomerase / chemistry*
  • Telomere / chemistry
  • Telomere Homeostasis
  • Telomere-Binding Proteins
  • Tetrahymena / enzymology*

Substances

  • DNA, Single-Stranded
  • Holoenzymes
  • Protein Subunits
  • Replication Protein A
  • Telomere-Binding Proteins
  • telomerase RNA
  • RNA
  • Telomerase

Associated data

  • PDB/2N6Q
  • PDB/5DFM
  • PDB/5DFN