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The caudal-related homeodomain protein Cdx-2/3 regulates glucagon gene expression in islet cells.

作者信息

Laser B, Meda P, Constant I, Philippe J

机构信息

Clinical Diabetology, Department of Medicine, Centre Médical Universitaire, 1 rue Michel Servet, CH-1211 Geneva 4, Switzerland.

出版信息

J Biol Chem. 1996 Nov 15;271(46):28984-94. doi: 10.1074/jbc.271.46.28984.

DOI:10.1074/jbc.271.46.28984
PMID:8910549
Abstract

Glucagon gene transcription in the endocrine pancreas is regulated by at least four cis-acting DNA control elements. We showed previously that G1 is critical for alpha cell-specific expression. G1 contains three AT-rich sequences important for promoter function, which represent candidate binding sites for homeodomain transcription factors. Performing reverse transcription-polymerase chain reaction amplifications with degenerate oligonucleotide primers homologous to the Antennapedia homeobox, cDNA clones corresponding to the caudal-related gene cdx-2/3 were predominantly obtained from glucagon-producing cells and primary non-beta cells. From RNase protection and polymerase chain reaction analyses, cdx-2/3 turned out to be the only caudal-related gene that is expressed at significant levels in cells of the endocrine pancreas. Cdx-2/3 binds with high affinity to an AT-rich motif of G1, which matches the consensus binding site of caudal-related proteins. In the glucagon-producing hamster cell line InR1G9, Cdx-2/3 is a subunit of complex B3 formed on G1. Alternative splicing generates two cdx-2/3 transcripts in islet cells, coding for a full-length protein and an amino-terminally truncated isoform. Although both isoforms bind G1 with similar affinity, only the full-length Cdx-2/3 A protein activates glucagon gene transcription in non-glucagon-producing cells, transcriptional activation being dose-dependent. We therefore conclude that the caudal-related gene cdx-2/3 is implicated in the transcriptional control of glucagon gene expression in the alpha cells of the islets of Langerhans.

摘要

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J Biol Chem. 1996 Nov 15;271(46):28984-94. doi: 10.1074/jbc.271.46.28984.
2
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