A mouse renin promoter containing the conserved decanucleotide element binds the same B‐cell factors as an authentic immunoglobulin heavy chain promoter
- 5 October 1987
- journal article
- Published by Wiley in FEBS Letters
- Vol. 222 (2) , 337-340
- https://doi.org/10.1016/0014-5793(87)80397-6
Abstract
A mouse renin‐1 gene promoter fragment, normally inactive in B‐cells, becomes a potent promoter in these cells after insertion of the highly conserved decanucleotide (dc/cd sequence) of immunoglobulin heavy and light chain promoters [(1987) EMBO J. 6, 1685–1690]. We observe retarded complexes of the same electrophoretic mobility when the cd‐containing renin promoter fragment or an authentic immunoglobulin heavy chain promoter fragment is incubated with a nuclear extract from myeloma cells, suggesting that the renin promoter is activated due to its acquired ability to bind a B‐cell‐specific positive factor. No retarded complexes are observed with the original renin promoter fragment thus questioning the presence of a repressor as an explanation for its lack of activity in B‐cells.Keywords
This publication has 20 references indexed in Scilit:
- Protein-nucleotide contacts in the immunoglobulin heavy-chain promoter region.Proceedings of the National Academy of Sciences, 1987
- A lymphoid-specific protein binding to the octamer motif of immunoglobulin genesNature, 1986
- Interaction of cell-type-specific nuclear proteins with immunoglobulin VH promoter region sequencesNature, 1986
- Multiple nuclear factors interact with the immunoglobulin enhancer sequencesCell, 1986
- A nuclear factor that binds to a conserved sequence motif in transcriptional control elements of immunoglobulin genesNature, 1986
- Analysis of promoter and enhancer cell type specificities and the regulation of immunoglobulin gene expressionGene, 1986
- Correct transcription of an immunoglobulin κ gene requires an upstream fragment containing conserved sequence elementsNature, 1984
- Structure of the 5' ends of immunoglobulin genes: a novel conserved sequence.Proceedings of the National Academy of Sciences, 1984
- Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nucleiNucleic Acids Research, 1983
- Continuous cultures of fused cells secreting antibody of predefined specificityNature, 1975