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Publication : Oct-2, although not required for early B-cell development, is critical for later B-cell maturation and for postnatal survival.

First Author  Corcoran LM Year  1993
Journal  Genes Dev Volume  7
Issue  4 Pages  570-82
PubMed ID  8096198 Mgi Jnum  J:4555
Mgi Id  MGI:53043 Doi  10.1101/gad.7.4.570
Citation  Corcoran LM, et al. (1993) Oct-2, although not required for early B-cell development, is critical for later B-cell maturation and for postnatal survival. Genes Dev 7(4):570-82
abstractText  Oct-2, a POU homeo domain transcription factor, is believed to stimulate B-cell-restricted expression of immunoglobulin genes through binding sites in immunoglobulin gene promoters and enhancers. To determine whether Oct-2 is required for B-cell development or function, or has other developmental roles, the gene was disrupted by homologous recombination. Oct-2-l- mice develop normally but die within hours of birth for undetermined reasons. Mutants contain normal numbers of B-cell precursors but are somewhat deficient in IgM+ B cells. These B cells have a marked defect in their capacity to secrete immunoglobulin upon mitogenic stimulation in vitro. Thus, Oct-2 is not required for the generation of immunoglobulin-bearing B cells but is crucial for their maturation to immunoglobulin-secreting cells and for another undetermined organismal function.
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