Mutations at the BLK locus linked to maturity onset diabetes of the young and β-cell dysfunction

  1. Maciej Borowieca,b,c,1,
  2. Chong W. Liewa,b,1,
  3. Ryan Thompsona,
  4. Watip Boonyasrisawata,b,2,
  5. Jiang Hua,
  6. Wojciech M. Mlynarskic,
  7. Ilham El Khattabia,b,
  8. Sung-Hoon Kima,b,
  9. Lorella Marsellia,b,
  10. Stephen S. Richd,
  11. Andrzej S. Krolewskia,b,
  12. Susan Bonner-Weira,b,
  13. Arun Sharmaa,b,
  14. Michele Saled,
  15. Josyf C. Mychaleckyjd,
  16. Rohit N. Kulkarnia,b and
  17. Alessandro Doriaa,b,3
  1. aResearch Division, Joslin Diabetes Center and
  2. bDepartment of Medicine, Harvard Medical School, Boston, MA 02215;
  3. cDepartment of Pediatrics, Medical University of Lodz, 91-738, Lodz, Poland; and
  4. dCenter for Public Health Genomics, University of Virginia, Charlottesville, VA 22908
  1. 2Present address: Department of Immunology, Siriraj Hospital Mahidol University, Bangkok 10700, Thailand.

  1. 1M.B. and C.W.L. contributed equally to this work.

  2. Communicated by C. Ronald Kahn, Harvard Medical School, Boston, MA, June 12, 2009 (received for review February 5, 2009)

Abstract

Maturity-onset diabetes of the young (MODY) is a subtype of diabetes defined by an autosomal pattern of inheritance and a young age at onset, often before age 25. MODY is genetically heterogeneous, with 8 distinct MODY genes identified to date and more believed to exist. We resequenced 732 kb of genomic sequence at 8p23 in 6 MODY families unlinked to known MODY genes that showed evidence of linkage at that location. Of the 410 sequence differences that we identified, 5 had a frequency <1% in the general population and segregated with diabetes in 3 of the families, including the 2 showing the strongest support for linkage at this location. The 5 mutations were all placed within 100 kb corresponding to the BLK gene. One resulted in an Ala71Thr substitution; the other 4 were noncoding and determined decreased in vitro promoter activity in reporter gene experiments. We found that BLK—a nonreceptor tyrosine-kinase of the src family of proto-oncogenes—is expressed in β-cells where it enhances insulin synthesis and secretion in response to glucose by up-regulating transcription factors Pdx1 and Nkx6.1. These actions are greatly attenuated by the Ala71Thr mutation. These findings point to BLK as a previously unrecognized modulator of β-cell function, the deficit of which may lead to the development of diabetes.

Footnotes

  • 3To whom correspondence should be addressed at: Section on Genetics and Epidemiology, Joslin Diabetes Center, One Joslin Place, Boston, MA 02215. E-mail: alessandro.doria{at}joslin.harvard.edu
  • Author contributions: M.B., C.W.L., S.B.-W., A.S., R.N.K., and A.D. designed research; M.B., C.W.L., R.T., W.B., J.H., W.M.M., I.E.K., S.-H.K., L.M., A.S.K., S.B.-W., A.S., M.S., R.N.K., and A.D. performed research; L.M. contributed new reagents/analytic tools; M.B., C.W.L., R.T., W.B., J.H., W.M.M., I.E.K., S.-H.K., L.M., A.S.K., S.B.-W., A.S., M.S., J.C.M., R.N.K., and A.D. analyzed data; and M.B., C.W.L., S.S.R., S.B.-W., A.S., J.C.M., R.N.K., and A.D. wrote the paper.

  • The authors declare no conflict of interest.