Meyer K B, Ireland J
Wellcome/CRC Institute of Cancer and Developmental Biology, Cambridge, UK.
Nucleic Acids Res. 1994 May 11;22(9):1576-82. doi: 10.1093/nar/22.9.1576.
Both the kappa intron and the kappa 3' enhancer are required for high levels of immunoglobulin kappa gene expression. The activity of both enhancer elements can be induced by LPS in pre-B cells. While the LPS induction of the kappa intron enhancer is mediated by NF-kappa B, this factor is not responsible for activation of the 3' enhancer. Dissection of the 3' enhancer has shown that in pre-B cells the activity of the kappa 3' enhancer is repressed by a region flanking an active core element. We have now scanned this flanking region for nuclear factor binding sites and have identified sites for B-cell specific E47/E12-like proteins and two ubiquitous nuclear proteins. Furthermore, we have identified a nuclear factor in pre-B cells whose binding activity is suppressed in response to LPS. In its tissue-distribution and binding specificity this factor appears to be identical to the lymphoid specific protein LEF-1. The position of the LEF-1 binding site within the 3' enhancer and its response to LPS raise the possibility that LEF-1 may be the target for a second pathway able to mediate LPS induction of immunoglobulin kappa gene transcription.
κ内含子和κ 3'增强子都是高水平免疫球蛋白κ基因表达所必需的。两种增强子元件的活性都可被前B细胞中的脂多糖(LPS)诱导。虽然κ内含子增强子的LPS诱导是由核因子κB介导的,但该因子并不负责3'增强子的激活。对3'增强子的剖析表明,在前B细胞中,κ 3'增强子的活性受到一个位于活性核心元件侧翼区域的抑制。我们现在已扫描该侧翼区域寻找核因子结合位点,并鉴定出了B细胞特异性E47/E12样蛋白和两种普遍存在的核蛋白的结合位点。此外,我们还在前B细胞中鉴定出一种核因子,其结合活性在LPS刺激下受到抑制。从其组织分布和结合特异性来看,该因子似乎与淋巴样特异性蛋白LEF-1相同。LEF-1结合位点在3'增强子中的位置及其对LPS的反应提示,LEF-1可能是能够介导LPS诱导免疫球蛋白κ基因转录的第二条信号通路的作用靶点。