Journal
HUMAN MOLECULAR GENETICS
Volume 22, Issue 17, Pages 3498-3507Publisher
OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddt204
Keywords
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Funding
- Canadian Institutes of Health Research [MOP-86672]
- Fonds de la Recherche en Sante du Quebec (FRSQ)
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Mutations in the dyskerin gene (DKC1) cause X-linked dyskeratosis congenita (DC), a rare and fatal premature aging syndrome characterized by defective telomere maintenance. Dyskerin is a highly conserved nucleolar protein, and a component of the human telomerase complex that is essential for human telomerase RNA (hTR) stability. However, its regulation remains poorly understood. Here, we report that dyskerin can be modified by small ubiquitin-like modifiers (SUMOs). We find that human DC-causing mutations in highly conserved dyskerin SUMOylation consensus sites lead to impaired hTR accumulation, telomerase activity and telomere maintenance. Finally, we show that modification of dyskerin by SUMOylation is required for its stability. Our findings provide the first evidence that dyskerin stability is regulated by SUMOylation and that mutations altering dyskerin SUMOylation can lead to defects in telomere maintenance that are characteristics of DC.
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