𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Transcription factors drive B cell development

✍ Scribed by James Hagman; Kara Lukin


Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
297 KB
Volume
18
Category
Article
ISSN
0952-7915

No coin nor oath required. For personal study only.

✦ Synopsis


Transcription factors including PU.1, E2A and early B cell factor (EBF) are essential for the earliest stages of B lymphocyte development. Recent advances suggest that, although PU.1 initiates events leading to B lymphopoiesis, it might be dispensable at later stages of development. E2A proteins are also crucial for B cell lineage determination, as shown by the pluripotency of E2A-deficient progenitors. Both PU.1 and E2A are required for expression of EBF. EBF activates the early program of genes unique to B cells, including the lineage commitment factor Pax5. EBF also facilitates the function of Pax5 by mediating epigenetic changes necessary for the function of Pax5 at gene targets. Together, these proteins function in a hierarchy of factors that orchestrates B cell development.


πŸ“œ SIMILAR VOLUMES


Expression of transcription factors duri
✍ Michael Wegner πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 139 KB

## Abstract Transcription factors coordinate the orderly changes of gene expression that underlie all developmental processes including those of oligodendrocytes. In comparison to other systems, relatively little is known about the role of transcription factors during oligodendrocyte development. H

B-cell development
✍ Norman R. Klinman; Dwane E. Wylie; Judy M. Teale πŸ“‚ Article πŸ“… 1981 πŸ› Elsevier Science 🌐 English βš– 497 KB
Transcriptional control during T-cell de
✍ Hans Clevers; Pierre Ferrier πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 English βš– 586 KB

During the past few years, the essential role of distinct transcription factors in specifying cell-fate decisions in a stepwise fashion during T-cell differentiation has been revealed. One striking feature is that a single factor can act at several sites throughout T-cell development, possibly throu