The SH2B gene is associated with serum leptin and body fat in normal female twins

  • Yalda Jamshidi
  • , Harold Snieder
  • , Dongliang Ge
  • , Tim D. Spector
  • , Sandra D. O'Dell*
  • *Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    43 Citations (Scopus)

    Abstract

    Src-homology-2 (SH2)-B, a Janus tyrosine kinase 2-interacting protein, has been identified recently as a key regulator of leptin and insulin sensitivity, glucose homeostasis, and body weight in mice. The aim of this study was to determine whether single-nucleotide polymorphisms (SNPs) in the human SH2B gene are associated with these variables. A tagging SNP (tSNP), Ala484Thr (rs7498665), was selected to represent five common SNPs (minor allele frequency > 0.05) in perfect linkage disequilibrium in a 16-kb region encompassing the SH2B gene. The tSNP was genotyped in 2455 white female twins (mean age, 47.4 +/- 12.6 years) from the St. Thomas' United Kingdom Adult Twin Registry (Twins United Kingdom). Ala484Thr (minor allele frequency, 0.38) was associated with serum leptin, total fat, waist circumference, and body weight (P = 0.02 to 0.04). The coding SNP has no predicted effect on protein structure or function and is likely to be in linkage disequilibrium with an as-yet unidentified functional variant in the SH2B gene. Our results support a role for SH2-B in modulating the regulation of body weight and fat by leptin in this female population. If SH2-B signaling is attenuated in diet-induced obesity, it could become a target for drug-induced leptin sensitization.

    Original languageEnglish
    Pages (from-to)5-9
    Number of pages5
    JournalObesity
    Volume15
    Issue number1
    DOIs
    Publication statusPublished - Jan-2007

    Keywords

    • fat distribution
    • genetic susceptibility
    • leptin
    • signal transduction
    • WEIGHT
    • SNPS
    • IDENTIFICATION
    • SENSITIVITY

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