Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.

Published

Journal Article

Nonsense-mediated mRNA decay (NMD) is of universal biological significance. It has emerged as an important global RNA, DNA and translation regulatory pathway. By systematically sequencing 737 genes (annotated in the Vertebrate Genome Annotation database) on the human X chromosome in 250 families with X-linked mental retardation, we identified mutations in the UPF3 regulator of nonsense transcripts homolog B (yeast) (UPF3B) leading to protein truncations in three families: two with the Lujan-Fryns phenotype and one with the FG phenotype. We also identified a missense mutation in another family with nonsyndromic mental retardation. Three mutations lead to the introduction of a premature termination codon and subsequent NMD of mutant UPF3B mRNA. Protein blot analysis using lymphoblastoid cell lines from affected individuals showed an absence of the UPF3B protein in two families. The UPF3B protein is an important component of the NMD surveillance machinery. Our results directly implicate abnormalities of NMD in human disease and suggest at least partial redundancy of NMD pathways.

Full Text

Duke Authors

Cited Authors

  • Tarpey, PS; Raymond, FL; Nguyen, LS; Rodriguez, J; Hackett, A; Vandeleur, L; Smith, R; Shoubridge, C; Edkins, S; Stevens, C; O'Meara, S; Tofts, C; Barthorpe, S; Buck, G; Cole, J; Halliday, K; Hills, K; Jones, D; Mironenko, T; Perry, J; Varian, J; West, S; Widaa, S; Teague, J; Dicks, E; Butler, A; Menzies, A; Richardson, D; Jenkinson, A; Shepherd, R; Raine, K; Moon, J; Luo, Y; Parnau, J; Bhat, SS; Gardner, A; Corbett, M; Brooks, D; Thomas, P; Parkinson-Lawrence, E; Porteous, ME; Warner, JP; Sanderson, T; Pearson, P; Simensen, RJ; Skinner, C; Hoganson, G; Superneau, D; Wooster, R; Bobrow, M; Turner, G; Stevenson, RE; Schwartz, CE; Futreal, PA; Srivastava, AK; Stratton, MR; Gécz, J

Published Date

  • September 2007

Published In

Volume / Issue

  • 39 / 9

Start / End Page

  • 1127 - 1133

PubMed ID

  • 17704778

Pubmed Central ID

  • 17704778

International Standard Serial Number (ISSN)

  • 1061-4036

Digital Object Identifier (DOI)

  • 10.1038/ng2100

Language

  • eng

Conference Location

  • United States