乘客5人
生物
心理压抑
B细胞
淋巴细胞生成
基因沉默
转录因子
细胞分化
基因表达调控
基因
细胞生物学
基因表达
遗传学
干细胞
祖细胞
抗体
作者
Sebastian Carotta,Melissa L. Holmes,Clare Pridans,Stephen L. Nutt
出处
期刊:Cell Cycle
[Informa]
日期:2006-10-18
卷期号:5 (21): 2452-2456
被引量:24
摘要
The transcription factor Pax5 is required for many aspects of B-lymphopoiesis including lineage commitment, immunoglobulin rearrangement, pre-BCR signalling and mature B cell survival. Pax5 regulates B cell lineage commitment by concurrently activating cell specific gene expression as well as suppressing the expression of genes associated with non-B cell fates. The identity of the molecular targets of Pax5-mediated gene repression is the subject of much current interest. Recent studies have documented the essential nature of the Pax5 mediated repression of the stem cell transcriptional program, as well as the silencing of lineage inappropriate gene expression, for B cell development. Surprisingly the repression of genes by Pax5 continues throughout lymphopoiesis, with the loss of Pax5 in mature B cell resulting in the reactivation of the same Pax5 targets during plasma cell differentiation. These recent insights into the mechanism of action of Pax5 in controlling B cell identity will be discussed.
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