help button home button Endocrine Society Molecular Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Beimesche, S.
Right arrow Articles by Knepel, W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Beimesche, S.
Right arrow Articles by Knepel, W.
Molecular Endocrinology 13 (5): 718-728
Copyright © 1999 by The Endocrine Society

Tissue-Specific Transcriptional Activity of a Pancreatic Islet Cell-Specific Enhancer Sequence/Pax6-Binding Site Determined in Normal Adult Tissues in Vivo Using Transgenic Mice

Stephan Beimesche, Andrea Neubauer, Stephan Herzig, Rafal Grzeskowiak, Thomas Diedrich, Irmgard Cierny, Doris Scholz, Tahseen Alejel and Willhart Knepel

Department of Molecular Pharmacology University of Göttingen D-37075 Göttingen, Germany

A pancreatic islet cell-specific enhancer sequence (PISCES) shared by the rat insulin-I, glucagon, and somatostatin genes binds the paired domain-containing transcription factor Pax6 and confers strong transcriptional activity in pancreatic islet cell lines. It was found recently that Pax6 plays a major role in islet development. In the present study, transgenic mice were used to investigate PISCES-mediated transcription in normal adult islets in vivo. In several independent mouse lines expressing a PISCES-luciferase reporter transgene, the PISCES motif directed gene expression in the adult eye, cerebellum, and discrete brain areas, consistent with the tissue distribution of Pax6. These tissues contain two Pax6 isoforms caused by alternative splicing, only one of which was found to bind the PISCES motif in electrophoretic mobility shift assays. No reporter gene expression was detected in adult pancreatic islets or in any other peripheral organ tested. RT-PCR analysis confirmed that Pax6 mRNA is present in adult islets. These results demonstrate that the PISCES motif is sufficient to direct highly tissue-specific gene expression in whole animals. The lack of PISCES-mediated transcription in adult islets indicates that the Pax6 protein(s) expressed in adult pancreatic islets function differently from the ones in the eye and cerebellum.




This article has been cited by other articles:


Home page
EndocrinologyHome page
J. Lu, G. Li, M. S. Lan, S. Zhang, W. Fan, H. Wang, and D. Lu
Pax4 Paired Domain Mediates Direct Protein Transduction into Mammalian Cells
Endocrinology, November 1, 2007; 148(11): 5558 - 5565.
[Abstract] [Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
A. S. Narang and R. I. Mahato
Biological and biomaterial approaches for improved islet transplantation.
Pharmacol. Rev., June 1, 2006; 58(2): 194 - 243.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Schinner, A. Barthel, C. Dellas, R. Grzeskowiak, S. K. Sharma, E. Oetjen, R. Blume, and W. Knepel
Protein Kinase B Activity Is Sufficient to Mimic the Effect of Insulin on Glucagon Gene Transcription
J. Biol. Chem., February 25, 2005; 280(8): 7369 - 7376.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
E. Oetjen, D. Baun, S. Beimesche, D. Krause, I. Cierny, R. Blume, C. Dickel, S. Wehner, and W. Knepel
Inhibition of Human Insulin Gene Transcription by the Immunosuppressive Drugs Cyclosporin A and Tacrolimus in Primary, Mature Islets of Transgenic Mice
Mol. Pharmacol., June 1, 2003; 63(6): 1289 - 1295.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Z. Ni, Y. Anini, X. Fang, G. Mills, P. L Brubaker, and T. Jin
Transcriptional Activation of the Proglucagon Gene by Lithium and beta -Catenin in Intestinal Endocrine L Cells
J. Biol. Chem., January 3, 2003; 278(2): 1380 - 1387.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. Grzeskowiak, J. Amin, E. Oetjen, and W. Knepel
Insulin Responsiveness of the Glucagon Gene Conferred by Interactions between Proximal Promoter and More Distal Enhancer-like Elements Involving the Paired-domain Transcription Factor Pax6
J. Biol. Chem., September 22, 2000; 275(39): 30037 - 30045.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Herzig, L. Fuzesi, and W. Knepel
Heterodimeric Pbx-Prep1 Homeodomain Protein Binding to the Glucagon Gene Restricting Transcription in a Cell Type-dependent Manner
J. Biol. Chem., September 1, 2000; 275(36): 27989 - 27999.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Schinner, C. Dellas, M. Schroder, C. A. Heinlein, C. Chang, J. Fischer, and W. Knepel
Repression of Glucagon Gene Transcription by Peroxisome Proliferator-activated Receptor gamma through Inhibition of Pax6 Transcriptional Activity
J. Biol. Chem., January 11, 2002; 277(3): 1941 - 1948.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1999 by The Endocrine Society