z-logo
open-access-imgOpen Access
Structure and function of the telomeric CST complex
Author(s) -
Cory Rice,
Emmanuel Skordalakes
Publication year - 2016
Publication title -
computational and structural biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.908
H-Index - 45
ISSN - 2001-0370
DOI - 10.1016/j.csbj.2016.04.002
Subject(s) - shelterin , telomere , telomere binding protein , biology , telomerase , rap1 , genome , microbiology and biotechnology , primase , ribonucleoprotein , genetics , dna replication , dna , computational biology , rna , reverse transcriptase , dna binding protein , gene , transcription factor
Telomeres comprise the ends of eukaryotic chromosomes and are essential for cell proliferation and genome maintenance. Telomeres are replicated by telomerase, a ribonucleoprotein (RNP) reverse transcriptase, and are maintained primarily by nucleoprotein complexes such as shelterin (TRF1, TRF2, TIN2, RAP1, POT1, TPP1) and CST (Cdc13/Ctc1, Stn1, Ten1). The focus of this review is on the CST complex and its role in telomere maintenance. Although initially thought to be unique to yeast, it is now evident that the CST complex is present in a diverse range of organisms where it contributes to genome maintenance. The CST accomplishes these tasks via telomere capping and by regulating telomerase and DNA polymerase alpha-primase (polα-primase) access to telomeres, a process closely coordinated with the shelterin complex in most organisms. The goal of this review is to provide a brief but comprehensive account of the diverse, and in some cases organism-dependent, functions of the CST complex and how it contributes to telomere maintenance and cell proliferation.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom