A B-cell-specific nuclear protein that binds to DNA sites 5' to immunoglobulin S alpha tandem repeats is regulated during differentiation
Waters, S. H. ; Saikh, K. U. ; Stavnezer, Janet
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Keywords
B-Lymphocytes
Base Sequence
Cell Line
Cloning, Molecular
DNA
DNA-Binding Proteins
*Genes, Immunoglobulin
Immunoglobulin Heavy Chains
Methylation
Molecular Sequence Data
Nuclear Proteins
Nucleotide Mapping
Recombination, Genetic
Restriction Mapping
Life Sciences
Medicine and Health Sciences
Women's Studies
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Abstract
Immunoglobulin heavy-chain switching is effected by recombination events between sites associated with tandemly repeated switch sequences located 5' to immunoglobulin heavy-chain genes. Using the band mobility shift assay, we have identified two distinct sites 5' to the alpha heavy-chain switch sequence with affinity for a single B-cell-specific DNA-binding protein, S alpha-BP. S alpha-BP was present in nuclear extracts from pre-B and B cells but was not detected in extracts from plasmacytomas, B-cell hybridomas, T-cell lymphomas, or a macrophage cell line. It was also not detectable in other nonlymphoid cells tested. Evidence suggests there are S alpha-BP-binding sites near other immunoglobulin switch sequences. As with the S alpha sites, these sites appear to be distinct from the consensus tandem repeats characteristic of immunoglobulin switch sequences. The possible functions of S alpha-BP on contacting its binding sites are discussed in the context of immunoglobulin heavy-chain switch recombination.
Source
Mol Cell Biol. 1989 Dec;9(12):5594-601.