Dominant-negative STAT1 SH2 domain mutations in unrelated patients with Mendelian susceptibility to mycobacterial disease

Hum Mutat. 2012 Sep;33(9):1377-87. doi: 10.1002/humu.22113. Epub 2012 Jun 7.

Abstract

Patients carrying two loss-of-function (or hypomorphic) alleles of STAT1 are vulnerable to intracellular bacterial and viral diseases. Heterozygosity for loss-of-function dominant-negative mutations in STAT1 is responsible for autosomal dominant (AD) Mendelian susceptibility to mycobacterial disease (MSMD), whereas heterozygosity for gain-of-function loss-of-dephosphorylation mutations causes AD chronic mucocutaneous candidiasis (CMC). The two previously reported types of AD MSMD-causing STAT1 mutations are located in the tail segment domain (p.L706S) or in the DNA-binding domain (p.E320Q and p.Q463H), whereas the AD CMC-causing mutations are located in the coiled-coil domain. We identified two cases with AD-STAT1 deficiency in two unrelated patients from Japan and Saudi Arabia carrying heterozygous missense mutations affecting the SH2 domain (p.K637E and p.K673R). p.K673R is a hypomorphic mutation that impairs STAT1 tyrosine phosphorylation, whereas the p.K637E mutation is null and affects both STAT1 phosphorylation and DNA-binding activity. Both alleles are dominant negative and result in impaired STAT1-mediated cellular responses to interferon (IFN)-γ and IL-27. In contrast, STAT1-mediated cellular responses against IFN-α and IFN-λ1 were preserved at normal levels in patients' cells. We describe here the first dominant mutations in the SH2 domain of STAT1, revealing the importance of this domain for tyrosine phosphorylation and DNA binding, as well as for antimycobacterial immunity.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Alleles
  • BCG Vaccine / adverse effects
  • Child
  • Cytokines / analysis
  • DNA Mutational Analysis
  • Disease Susceptibility / immunology
  • Disease Susceptibility / microbiology*
  • Disease Susceptibility / pathology
  • Female
  • Genes, Dominant
  • Humans
  • Infant
  • Interferon-alpha / pharmacology
  • Interferon-gamma / pharmacology
  • Interleukins / immunology
  • Interleukins / pharmacology
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / immunology
  • Loss of Heterozygosity
  • Male
  • Mutation, Missense*
  • Mycobacterium bovis / immunology
  • Mycobacterium tuberculosis / immunology
  • Mycobacterium tuberculosis / isolation & purification*
  • Mycobacterium tuberculosis / pathogenicity
  • Phosphorylation
  • Protein Multimerization
  • STAT1 Transcription Factor / genetics*
  • STAT1 Transcription Factor / immunology
  • STAT1 Transcription Factor / metabolism
  • Signal Transduction
  • Tuberculosis / immunology
  • Tuberculosis / microbiology
  • Tuberculosis / pathology
  • Tyrosine / metabolism
  • src Homology Domains*

Substances

  • BCG Vaccine
  • Cytokines
  • Interferon-alpha
  • Interleukins
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Tyrosine
  • Interferon-gamma