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Originally published In Press as doi:10.1074/jbc.M005704200 on August 9, 2000

J. Biol. Chem., Vol. 275, Issue 42, 32708-32715, October 20, 2000
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The Paired Homeodomain Transcription Factor Pax-2 Is Expressed in the Endocrine Pancreas and Transactivates the Glucagon Gene Promoter*

Beate Ritz-LaserDagger , Anne Estreicher, Benoit Gauthier, and Jacques Philippe

From the Diabetes Unit, Centre Médical Universitaire, 1211 Genève 4, Switzerland

Glucagon gene expression is controlled by at least four DNA elements within the promoter; G2, G3, and G4 confer islet-specific expression, while G1 restricts glucagon transcription to alpha  cells. Two islet-specific complexes are formed on G3, the insulin-responsive element of the glucagon gene; one of these corresponds to the paired homeodomain protein Pax-6, a major glucagon gene transactivator that plays a crucial role in alpha  cell development. We describe here the identification of the second complex as Pax-2, another member of the paired box family. Pax-2 is known to be crucial for the development of the urogenital tract and of the central nervous system, but its presence in the endocrine pancreas has not been reported. We detected Pax-2 gene expression by RT-PCR; in islets, Pax-2 is present as two alternative splicing isoforms, Pax-2A and Pax-2B, whereas in the glucagon- and insulin-producing cell lines alpha TC1 and Min6, a distinct isoform, Pax-2D2, is found in addition to Pax-2B. Both islet-specific isoforms bind to the enhancer element G3 and to the alpha -specific promoter element G1 that also interacts with Pax-6. Pax-2A and Pax-2B dose-dependently activate transcription from the G3 and the G1 elements both in heterologous and in glucagon-producing cells. Our data indicate that Pax-2 is the third paired domain protein present in the endocrine pancreas and that one of its roles may be the regulation of glucagon gene expression.


* This work was supported by the Swiss National Fund, the Institute for Human Genetics and Biochemistry, the Berger Foundation, and the Carlos and Elsie de Reuters Foundation.The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Dagger To whom correspondence should be addressed. Tel.: 41-22-702-55-67; Fax: 41-22-702-55-43; E-mail: Beate.Laser@medecine.unige.ch.


Copyright © 2000 by The American Society for Biochemistry and Molecular Biology, Inc.
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