A B-cell-specific nuclear protein that binds to DNA sites 5' to immunoglobulin S alpha tandem repeats is regulated during differentiation

Mol Cell Biol. 1989 Dec;9(12):5594-601. doi: 10.1128/mcb.9.12.5594-5601.1989.

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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • B-Lymphocytes / immunology*
  • Base Sequence
  • Cell Line
  • Cloning, Molecular
  • DNA / genetics*
  • DNA-Binding Proteins / metabolism*
  • Genes, Immunoglobulin*
  • Immunoglobulin Heavy Chains / genetics*
  • Methylation
  • Molecular Sequence Data
  • Nuclear Proteins / metabolism*
  • Nucleotide Mapping
  • Recombination, Genetic
  • Restriction Mapping

Substances

  • DNA-Binding Proteins
  • Immunoglobulin Heavy Chains
  • Nuclear Proteins
  • DNA