The HMG Box Transcription Factor Sox4 Contributes to the Development of the Endocrine Pancreas

  1. Maria E. Wilson1,
  2. Katherine Y. Yang1,
  3. Anna Kalousova1,
  4. Janet Lau1,
  5. Yasuhiro Kosaka1,
  6. Francis C. Lynn1,
  7. Juehu Wang1,
  8. Caroline Mrejen12,
  9. Vasso Episkopou3,
  10. Hans C. Clevers4 and
  11. Michael S. German15
  1. 1Diabetes Center, Hormone Research Institute, University of California at San Francisco, San Francisco, California
  2. 2Department of Cell and Tissue Biology, University of California at San Francisco, San Francisco, California
  3. 3Medical Research Council Clinical Sciences Centre, Imperial College, Faculty of Medicine, Hammersmith Hospital Campus, London, U.K
  4. 4Hubrecht Laboratory, Centre for Biomedical Genetics, Utrecht, Netherlands
  5. 5Department of Medicine, University of California at San Francisco, San Francisco, California
  1. Address correspondencereprint requests to Dr. Michael German, UCSF Diabetes Center, University of California San Francisco, 513 Parnassus Ave., San Francisco, CA 94143-0534. E-mail: mgerman{at}diabetes.ucsf.edu

Abstract

To investigate the role of the Sry/hydroxymethylglutaryl box (Sox) transcription factors in the development of the pancreas, we determined the expression pattern of Sox factors in the developing mouse pancreas. By RT-PCR, we detected the presence of multiple Sox family members in both the developing pancreas and mature islets and then focused on two factors, Sox2 and Sox4. The expression field of Sox2, which plays a role in the maintenance of some stem cell populations, included the developing duodenum, but Sox2 was specifically excluded from the pancreatic buds. In contrast, Sox4 was detected broadly in the early pancreatic buds and eventually became restricted to the nuclei of all islet cells in the adult mouse. Mice homozygous for a null mutation of the sox4 gene showed normal pancreatic bud formation and endocrine cell differentiation up to embryonic day 12.5. Beyond that date, cultured pancreatic explants lacking sox4 failed to form normal islets. Instead, a markedly reduced number of endocrine cells were found scattered through the explant. We show here that several Sox transcription factors are expressed in the developing pancreas and in the islet, and that one of these factors, Sox4, is required for the normal development of pancreatic islets.

Footnotes

  • M.E.W. is employed by and holds stock in Metabolex.

    • Accepted August 30, 2005.
    • Received June 13, 2005.
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