Abstract
The E2A gene products, E12 and E47, are required for proper B cell development. Mice lacking the E2A gene products generate only a very small number of B220+ cells, which lack immunoglobulin DJ(H) rearrangements. We have now generated mice expressing either E12 or E47. B cell development in mice expressing E12 but lacking E47 is perturbed at the pro-B cell stage, and these mice lack IgM+B220+ B cells in both bone marrow and spleen. IgM+B220+ B cells can be detected, albeit at significantly reduced levels, in the bone marrow and spleen of mice lacking E12. Ectopic expression of both E12 and E47 in a null mutant background shows that E12 and E47 act in concert to promote B lineage development. Taken together, the data indicate that both E12 and E47 allow commitment to the B cell lineage and act synergistically to promote B lymphocyte maturation.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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B-Lymphocytes / immunology*
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B-Lymphocytes / metabolism
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Cell Differentiation / drug effects
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Cell Differentiation / immunology
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DNA-Binding Proteins / biosynthesis
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DNA-Binding Proteins / genetics*
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DNA-Binding Proteins / pharmacology
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Drug Synergism
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Gene Rearrangement, B-Lymphocyte / genetics
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Gene Rearrangement, B-Lymphocyte / immunology
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Mice
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Mice, Mutant Strains
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Mice, Transgenic
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TCF Transcription Factors
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Transcription Factor 7-Like 1 Protein
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Transcription Factors / biosynthesis
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Transcription Factors / genetics
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Transcription Factors / pharmacology
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Transcription, Genetic / genetics
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Transcription, Genetic / immunology
Substances
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DNA-Binding Proteins
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TCF Transcription Factors
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Tcf7l1 protein, mouse
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Transcription Factor 7-Like 1 Protein
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Transcription Factors