Multiple DNA-protein interactions at the CpG island of the human pseudoautosomal geneMIC2
Autor: | A. Braghetti, Chiara Mondello, Luisa Lanfranco, G. Piazzi |
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Rok vydání: | 1993 |
Předmět: |
Transcription
Genetic Sp1 Transcription Factor Molecular Sequence Data Pseudoautosomal region 12E7 Antigen Biology Binding Competitive X-inactivation Antigens CD Genetics Humans Nuclear protein Binding site Gene Transcription factor Membrane Glycoproteins Base Sequence DNase-I Footprinting Gene Amplification DNA Cell Biology General Medicine Molecular biology DNA-Binding Proteins CpG site Female Cell Adhesion Molecules Dinucleoside Phosphates Pseudogenes HeLa Cells |
Zdroj: | Somatic Cell and Molecular Genetics. 19:51-63 |
ISSN: | 1572-9931 0740-7750 |
DOI: | 10.1007/bf01233954 |
Popis: | The human MIC2 gene is pseudoautosomal and in females it escapes X inactivation. At the 5' end of the gene a 1.2-kb-long CpG island has been identified that is unmethylated on the active X, the inactive X, and on the Y chromosome. We have demonstrated by 5' RACE experiments that this region contains the transcription start site of the gene. To better characterize this CpG island, we have investigated the interaction between this region and nuclear proteins in vitro by using DNA gel mobility shift and DNase I footprinting techniques. Band shift experiments with HeLa cell nuclear extract have indicated that all the island is involved in multiple interactions with nuclear proteins. Experiments with a eukaryotic purified Sp1 protein have shown that this factor specifically binds to several sites of the island. Three DNase I protected footprints have been identified in the region between nucleotides -122 and +34 with respect to the transcription initiation site. By using a recombinant Sp1 protein, we have shown that all the footprints are due to the binding of Sp1. The sequences of two footprints correspond to the decanucleotide binding site for Sp1, the sequence of the third one does not contain any published Sp1 recognition site. |
Databáze: | OpenAIRE |
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