Department of Human Genetics, University of Utah, Salt Lake City, United States
Kristin A Moore
Department of Biology, University of Utah, Salt Lake City, United States; Center for Cell and Genome Sciences, University of Utah, Salt Lake City, United States
Alex Chapin
Department of Human Genetics, University of Utah, Salt Lake City, United States
Julie Hollien
Department of Biology, University of Utah, Salt Lake City, United States; Center for Cell and Genome Sciences, University of Utah, Salt Lake City, United States
The nonsense-mediated mRNA decay (NMD) pathway functions to degrade both abnormal and wild-type mRNAs. NMD is essential for viability in most organisms, but the molecular basis for this requirement is unknown. Here we show that a single, conserved NMD target, the mRNA coding for the stress response factor growth arrest and DNA-damage inducible 45 (GADD45) can account for lethality in Drosophila lacking core NMD genes. Moreover, depletion of Gadd45 in mammalian cells rescues the cell survival defects associated with NMD knockdown. Our findings demonstrate that degradation of Gadd45 mRNA is the essential NMD function and, surprisingly, that the surveillance of abnormal mRNAs by this pathway is not necessarily required for viability.
