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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome.

Abstract
Mutations in LKB1 lead to Peutz-Jeghers syndrome (PJS). However, only a subset of PJS patients harbours LKB1 mutations. We performed a mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in 28 LKB1-negative PJS patients. No disease-causing mutations were detected in the studied genes in PJS patients from different European populations.
AuthorsP Alhopuro, P Katajisto, R Lehtonen, S K Ylisaukko-Oja, L Näätsaari, A Karhu, A M Westerman, J H P Wilson, F W M de Rooij, T Vogel, G Moeslein, I P Tomlinson, L A Aaltonen, T P Mäkelä, V Launonen
JournalBritish journal of cancer (Br J Cancer) Vol. 92 Issue 6 Pg. 1126-9 (Mar 28 2005) ISSN: 0007-0920 [Print] England
PMID15756273 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adaptor Proteins, Signal Transducing
  • Adaptor Proteins, Vesicular Transport
  • Nuclear Proteins
  • STRADA protein, human
  • Transcription Factors
  • SMARCA4 protein, human
  • DNA Helicases
Topics
  • Adaptor Proteins, Signal Transducing (genetics)
  • Adaptor Proteins, Vesicular Transport (genetics)
  • DNA Helicases
  • Humans
  • Introns
  • Mutation
  • Nuclear Proteins (genetics)
  • Peutz-Jeghers Syndrome (genetics)
  • Polymorphism, Genetic
  • Transcription Factors (genetics)

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