Deregulation of β-catenin signal byHelicobacter pyloriCagA requires the CagA-multimerization sequence


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Abstract

Infection withHelicobacter pylori cagA-positive strains causes gastritis and peptic ulceration and is associated with gastric adenocarcinoma. ThecagAgene product CagA is delivered into gastric epithelial cells, where it undergoes tyrosine phosphorylation by Src family kinases at the C-terminal EPIYA-repeat region. Tyrosine-phosphorylated CagA specifically binds and activates SHP-2 tyrosine phosphatase, causing cell morphological transformation known as the hummingbird phenotype. CagA also destabilizes the E-cadherin/β-catenin complex to elicit aberrant activation of the β-catenin signal that underlies intestinal metaplasia. Here we show that translocalization of membranous β-catenin and subsequent activation of the β-catenin signal by CagA requires the EPIYA-repeat region, which is characterized by structural variation between CagA ofH. pyloriisolated in Western countries (Western CagA) and that of East AsianH. pyloriisolates (East Asian CagA), but is independent of CagA tyrosine phosphorylation. Detailed analysis using a series of Western and East Asian CagA mutants revealed that deregulation of β-catenin requires residues 1009–1086 and residues 908–1012 of ABCCC Western CagA and ABD East Asian CagA, respectively, and is mediated by the 16-amino-acid CagA multimerization sequence that is conserved between the 2 geographically distinctH. pyloriCagA species. Our results indicate that aberrant activation of the β-catenin signal, which promotes precancerous intestinal metaplasia, is an inherent and fundamental CagA activity that is independent of the structural polymorphism of CagA.

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