In mammals, nonsense-mediated mRNA decay (NMD) is a quality-control mechanism that degrades mRNA harboring a premature termination codon to prevent the synthesis of truncated proteins. To gain insight into the NMD mechanism, we identified NMD inhibitor 1 (NMDI 1) as a small molecule inhibitor of the NMD pathway. We characterized the mode of action of this compound and demonstrated that it acts upstream of hUPF1. NMDI 1 induced the loss of interactions between hSMG5 and hUPF1 and the stabilization of hyperphosphorylated isoforms of hUPF1. Incubation of cells with NMDI 1 allowed us to demonstrate that NMD factors and mRNAs subject to NMD transit through processing bodies (P-bodies), as is the case in yeast. The results suggest a model in which mRNA and NMD factors are sequentially recruited to P-bodies.
Inhibition of nonsense-mediated mRNA decay (NMD) by a new chemical molecule reveals the dynamic of NMD factors in P-bodies
Abbreviations used in this paper: CHX, cycloheximide; DCP, decapping protein; EJC, exon junction complex; Fluc, firefly luciferase; Gl, β globin; GPx1, glutathione peroxidase 1; IP, immunoprecipitation; miRNA, microRNA; MUP, major urinary protein; NMD, nonsense-mediated mRNA decay; NMDI 1, NMD inhibitor 1; P-bodies, processing bodies; PTC, premature termination codon; Rluc, Renilla luciferase; RPA, RNase protection assay; SSC, sodium saline citrate.
Sébastien Durand, Nicolas Cougot, Florence Mahuteau-Betzer, Chi-Hung Nguyen, David S. Grierson, Edouard Bertrand, Jamal Tazi, Fabrice Lejeune; Inhibition of nonsense-mediated mRNA decay (NMD) by a new chemical molecule reveals the dynamic of NMD factors in P-bodies . J Cell Biol 24 September 2007; 178 (7): 1145–1160. doi: https://doi.org/10.1083/jcb.200611086
Download citation file:
Sign in
Client Account
Sign in via your Institution
Sign in via your InstitutionEmail alerts
Advertisement
Advertisement