Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.

Published

Journal Article

Noonan and LEOPARD syndromes are developmental disorders with overlapping features, including cardiac abnormalities, short stature and facial dysmorphia. Increased RAS signaling owing to PTPN11, SOS1 and KRAS mutations causes approximately 60% of Noonan syndrome cases, and PTPN11 mutations cause 90% of LEOPARD syndrome cases. Here, we report that 18 of 231 individuals with Noonan syndrome without known mutations (corresponding to 3% of all affected individuals) and two of six individuals with LEOPARD syndrome without PTPN11 mutations have missense mutations in RAF1, which encodes a serine-threonine kinase that activates MEK1 and MEK2. Most mutations altered a motif flanking Ser259, a residue critical for autoinhibition of RAF1 through 14-3-3 binding. Of 19 subjects with a RAF1 mutation in two hotspots, 18 (or 95%) showed hypertrophic cardiomyopathy (HCM), compared with the 18% prevalence of HCM among individuals with Noonan syndrome in general. Ectopically expressed RAF1 mutants from the two HCM hotspots had increased kinase activity and enhanced ERK activation, whereas non-HCM-associated mutants were kinase impaired. Our findings further implicate increased RAS signaling in pathological cardiomyocyte hypertrophy.

Full Text

Duke Authors

Cited Authors

  • Pandit, B; Sarkozy, A; Pennacchio, LA; Carta, C; Oishi, K; Martinelli, S; Pogna, EA; Schackwitz, W; Ustaszewska, A; Landstrom, A; Bos, JM; Ommen, SR; Esposito, G; Lepri, F; Faul, C; Mundel, P; López Siguero, JP; Tenconi, R; Selicorni, A; Rossi, C; Mazzanti, L; Torrente, I; Marino, B; Digilio, MC; Zampino, G; Ackerman, MJ; Dallapiccola, B; Tartaglia, M; Gelb, BD

Published Date

  • August 2007

Published In

Volume / Issue

  • 39 / 8

Start / End Page

  • 1007 - 1012

PubMed ID

  • 17603483

Pubmed Central ID

  • 17603483

International Standard Serial Number (ISSN)

  • 1061-4036

Digital Object Identifier (DOI)

  • 10.1038/ng2073

Language

  • eng

Conference Location

  • United States