Miyazaki Kazuko, Miyazaki Masaki, Murre Cornelis
Department of Molecular Biology, University of California, San Diego, La Jolla, CA 92093, USA.
Department of Molecular Biology, University of California, San Diego, La Jolla, CA 92093, USA.
Trends Immunol. 2014 May;35(5):205-10. doi: 10.1016/j.it.2014.02.009. Epub 2014 Mar 26.
In B cell progenitors, E-proteins E2A and HEB (HeLa E-box binding protein) are crucial for the induction of a B lineage-specific program of gene expression and for orchestrating the assembly of the immunoglobulin loci. In the thymus E2A and HEB act differently, activating the expression of genes closely associated with the establishment of T cell identity and promoting the rearrangement of T cell receptor (TCR) loci. These findings have raised the question as to how E-proteins exert these different activities. We review here the distinct regulatory networks that establish B versus T cell identity, and how genomic architecture and location of genes is modulated in these lineage decisions. We conclude by proposing a model wherein stochasticity in the nuclear location of the early B cell factor 1 (Ebf1) locus in multipotent progenitors determines this lineage choice.
在B细胞祖细胞中,E蛋白E2A和HEB(HeLa E盒结合蛋白)对于诱导B谱系特异性基因表达程序以及协调免疫球蛋白基因座的组装至关重要。在胸腺中,E2A和HEB的作用不同,它们激活与T细胞身份确立密切相关的基因表达,并促进T细胞受体(TCR)基因座的重排。这些发现引发了一个问题,即E蛋白如何发挥这些不同的活性。我们在此回顾建立B细胞与T细胞身份的不同调控网络,以及在这些谱系决定中基因的基因组结构和位置是如何被调节的。我们通过提出一个模型来总结,即多能祖细胞中早期B细胞因子1(Ebf1)基因座核定位的随机性决定了这种谱系选择。