Mutations at the BLK locus linked to maturity onset diabetes of the young and β-cell dysfunction
- Maciej Borowieca,b,c,1,
- Chong W. Liewa,b,1,
- Ryan Thompsona,
- Watip Boonyasrisawata,b,2,
- Jiang Hua,
- Wojciech M. Mlynarskic,
- Ilham El Khattabia,b,
- Sung-Hoon Kima,b,
- Lorella Marsellia,b,
- Stephen S. Richd,
- Andrzej S. Krolewskia,b,
- Susan Bonner-Weira,b,
- Arun Sharmaa,b,
- Michele Saled,
- Josyf C. Mychaleckyjd,
- Rohit N. Kulkarnia,b and
- Alessandro Doriaa,b,3
- aResearch Division, Joslin Diabetes Center and
- bDepartment of Medicine, Harvard Medical School, Boston, MA 02215;
- cDepartment of Pediatrics, Medical University of Lodz, 91-738, Lodz, Poland; and
- dCenter for Public Health Genomics, University of Virginia, Charlottesville, VA 22908
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↵2Present address: Department of Immunology, Siriraj Hospital Mahidol University, Bangkok 10700, Thailand.
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↵1M.B. and C.W.L. contributed equally to this work.
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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
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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.
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The authors declare no conflict of interest.










