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 Previous Article

Molecular and Cellular Biology, April 2009, p. 2322-2334, Vol. 29, No. 8
0270-7306/09/$08.00+0     doi:10.1128/MCB.01543-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Pax6 Regulates the Proglucagon Processing Enzyme PC2 and Its Chaperone 7B2{triangledown} ,{dagger}

Liora S. Katz,* Yvan Gosmain, Eric Marthinet, and Jacques Philippe

Diabetes Unit, Division of Endocrinology, Diabetes and Nutrition, University Hospital, University of Geneva Medical School, 1211 Geneva, Switzerland

Received 3 October 2008/ Returned for modification 30 November 2008/ Accepted 31 January 2009

Pax6 is important in the development of the pancreas and was previously shown to regulate pancreatic endocrine differentiation, as well as the insulin, glucagon, and somatostatin genes. Prohormone convertase 2 (PC2) is the main processing enzyme in pancreatic {alpha} cells, where it processes proglucagon to produce glucagon under the spatial and temporal control of 7B2, which functions as a molecular chaperone. To investigate the role of Pax6 in glucagon biosynthesis, we studied potential target genes in InR1G9 {alpha} cells transfected with Pax6 small interfering RNA and in InR1G9 clones expressing a dominant-negative form of Pax6. We now report that Pax6 controls the expression of the PC2 and 7B2 genes. By binding and transactivation studies, we found that Pax6 indirectly regulates PC2 gene transcription through cMaf and Beta2/NeuroD1 while it activates the 7B2 gene both directly and indirectly through the same transcription factors, cMaf and Beta2/NeuroD1. We conclude that Pax6 is critical for glucagon biosynthesis and processing by directly and indirectly activating the glucagon gene through cMaf and Beta2/NeuroD1, as well as the PC2 and 7B2 genes.


* Corresponding author. Mailing address: Diabetes Unit, University Hospital, 1211 Geneva, Switzerland. Phone: 41 22 3724237. Fax: 41 22 3729326. E-mail: Liora.Katz{at}unige.ch

{triangledown} Published ahead of print on 17 February 2009.

{dagger} Supplemental material for this article may be found at http://mcb.asm.org/.


Molecular and Cellular Biology, April 2009, p. 2322-2334, Vol. 29, No. 8
0270-7306/09/$08.00+0     doi:10.1128/MCB.01543-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.