کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3354148 | 1216914 | 2007 | 11 صفحه PDF | دانلود رایگان |

SummaryGA binding protein (GABP) is a ubiquitously expressed Ets-family transcription factor that critically regulates the expression of the interleukin-7 receptor α chain (IL-7Rα) in T cells, whereas it is dispensable for IL-7Rα expression in fetal liver B cells. Here we showed that deficiency of GABPα, the DNA-binding subunit of GABP, resulted in profoundly defective B cell development and a compromised humoral immune response, in addition to thymic developmental defects. Furthermore, the expression of Pax5 and Pax5 target genes such as Cd79a was greatly diminished in GABPα-deficient B cell progenitors, pro-B, and mature B cells. GABP could bind to the regulatory regions of Pax5 and Cd79a in vivo. Thus, GABP is a key regulator of B cell development, maturation, and function.
Journal: - Volume 26, Issue 4, 27 April 2007, Pages 421–431