The multiple lives of NMD factors: Balancing roles in gene and genome regulation

Olaf Isken, Lynne E. Maquat

253 Citations (Scopus)

Abstract

Nonsense-mediated mRNA decay (NMD) largely functions to ensure the quality of gene expression. However, NMD is also crucial to regulating appropriate expression levels for certain genes and for maintaining genome stability. Furthermore, just as NMD serves cells in multiple ways, so do its constituent proteins. Recent studies have clarified that UPF and SMG proteins, which were originally discovered to function in NMD, also have roles in other pathways, including specialized pathways of mRNA decay, DNA synthesis and cell-cycle progression, and the maintenance of telomeres. These findings suggest a delicate balance of metabolic events - some not obviously related to NMD - that can be influenced by the cellular abundance, location and activity of NMD factors and their binding partners.

Original languageEnglish
JournalNature Reviews Genetics
Volume9
Issue number9
Pages (from-to)699-712
Number of pages14
ISSN1471-0056
DOIs
Publication statusPublished - 01.09.2008

Funding

We thank C. Woeller for reading the manuscript and help with its formatting and G. Chanfreau for conversations. The Maquat lab is supported by NIH R01 grants GM074593 and GM059514 to L.E.M.

Research Areas and Centers

  • Academic Focus: Center for Infection and Inflammation Research (ZIEL)

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