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Live Cell Imaging Reveals the Dynamics of Telomerase Recruitment to Telomeres.
Schmidt, Jens C; Zaug, Arthur J; Cech, Thomas R.
Afiliação
  • Schmidt JC; Howard Hughes Medical Institute, Department of Chemistry and Biochemistry, BioFrontiers Institute, University of Colorado Boulder, Boulder, CO 80309, USA.
  • Zaug AJ; Howard Hughes Medical Institute, Department of Chemistry and Biochemistry, BioFrontiers Institute, University of Colorado Boulder, Boulder, CO 80309, USA.
  • Cech TR; Howard Hughes Medical Institute, Department of Chemistry and Biochemistry, BioFrontiers Institute, University of Colorado Boulder, Boulder, CO 80309, USA. Electronic address: thomas.cech@colorado.edu.
Cell ; 166(5): 1188-1197.e9, 2016 Aug 25.
Article em En | MEDLINE | ID: mdl-27523609
Telomerase maintains genome integrity by adding repetitive DNA sequences to the chromosome ends in actively dividing cells, including 90% of all cancer cells. Recruitment of human telomerase to telomeres occurs during S-phase of the cell cycle, but the molecular mechanism of the process is only partially understood. Here, we use CRISPR genome editing and single-molecule imaging to track telomerase trafficking in nuclei of living human cells. We demonstrate that telomerase uses three-dimensional diffusion to search for telomeres, probing each telomere thousands of times each S-phase but only rarely forming a stable association. Both the transient and stable association events depend on the direct interaction of the telomerase protein TERT with the telomeric protein TPP1. Our results reveal that telomerase recruitment to telomeres is driven by dynamic interactions between the rapidly diffusing telomerase and the chromosome end.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Telômero / Telomerase Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Telômero / Telomerase Idioma: En Ano de publicação: 2016 Tipo de documento: Article