Erman B, Cortes M, Nikolajczyk B S, Speck N A, Sen R
Rosenstiel Research Center and Department of Biology, Brandeis University, Waltham, Massachusetts 02254, USA.
Mol Cell Biol. 1998 Mar;18(3):1322-30. doi: 10.1128/MCB.18.3.1322.
A tripartite domain of the murine immunoglobulin mu heavy-chain enhancer contains the muA and muB elements that bind ETS proteins and the muE3 element that binds leucine zipper-containing basic helix-loop-helix (bHLH-zip) factors. Analysis of the corresponding region of the human mu enhancer revealed high conservation of the muA and muB motifs but a striking absence of the muE3 element. Instead of bHLH-zip proteins, we found that the human enhancer bound core binding factor (CBF) between the muA and mu elements; CBF binding was shown to be a common feature of both murine and human enhancers. Furthermore, mutant enhancers that bound prototypic bHLH-zip proteins but not CBF did not activate transcription in B cells, and conversely, CBF transactivated the murine enhancer in nonlymphoid cells. Taking these data together with the earlier analysis of T-cell-specific enhancers, we propose that ETS-CBF is a common composite element in the regulation of antigen receptor genes. In addition, these studies identify the first B-cell target of CBF, a protein that has been implicated in the development of childhood pre-B-cell leukemias.
小鼠免疫球蛋白μ重链增强子的一个三方结构域包含结合ETS蛋白的μA和μB元件以及结合含亮氨酸拉链的碱性螺旋-环-螺旋(bHLH-zip)因子的μE3元件。对人类μ增强子相应区域的分析显示,μA和μB基序高度保守,但μE3元件明显缺失。我们发现,人类增强子在μA和μ元件之间结合核心结合因子(CBF),而不是bHLH-zip蛋白;CBF结合被证明是小鼠和人类增强子的共同特征。此外,结合原型bHLH-zip蛋白但不结合CBF的突变增强子在B细胞中不激活转录,相反,CBF在非淋巴细胞中反式激活小鼠增强子。将这些数据与早期对T细胞特异性增强子的分析相结合,我们提出ETS-CBF是抗原受体基因调控中的一个常见复合元件。此外,这些研究确定了CBF的首个B细胞靶点,CBF是一种与儿童前B细胞白血病发生有关的蛋白。