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Complete block of early B cell differentiation and altered patterning of the posterior midbrain in mice lacking Pax5/BSAP
Abstract
The Pax5 gene, coding for the transcription factor BSAP, was mutated in the mouse germline by targeted disruption. Homozygous mutant mice were born alive, became growth retarded, and usually died within three weeks. About 5% of mutants survived to adulthood and were fertile, but severely runted. Morphogenesis of the posterior midbrain was affected as early as embryonic day 16.5, leading to a reduction of the inferior colliculus near the midline and to altered foliation of the anterior cerebellum. Moreover, all mutants failed to produce small pre-B, B, and plasma cells owing to a complete arrest of B cell development at an early precursor stage. These data define a key role for Pax5 in early B lymphopoiesis and midbrain patterning.
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Developmental progression of B cells is critically dependent on activity of various transcription factors binding to promoter and enhancer elements of Ig genes.
“In fact, gene-targeting studies indicate that the developmental progression of B cells is critically dependent on the activity of various transcription factors, which bind to promoter and enhancer elements of Ig genes (heavy and light chains), suggesting a link between the signal transduction and transcription factors during B-cell development (13-18”
From AKT Induces Transcriptional Activity of PU.1 through Phosphorylation-mediated Modifications within Its Transactivation Domain (2001) · cites this paper as [17]
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Metadata
- Authors
- URBANEK, P.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1994-12
- Volume
- 79
- Issue
- 5
- Pages
- 901-912
- ISSN
- 0092-8674
- Cited by
- 670
- References
- 1
- Language
- en
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