Baldwin A S, LeClair K P, Singh H, Sharp P A
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Mol Cell Biol. 1990 Apr;10(4):1406-14. doi: 10.1128/mcb.10.4.1406-1414.1990.
A cDNA from a B-cell library was previously isolated that encodes a sequence-specific DNA-binding protein with affinities for related sites in a class I major histocompatibility complex (MHC) and kappa immunoglobulin gene enhancers. We report here approximately 6.5 kilobases of sequence of the MBP-1 (MHC enhancer binding protein 1) cDNA. MBP-1 protein has a molecular weight predicted to be greater than 200,000. A DNA-binding domain with high affinity for the MHC enhancer sequence TGGGGATTCCCCA was localized to an 118-amino-acid protein fragment containing two zinc fingers of the class Cys2-X12-His2. Analysis of expression of MBP-1 mRNA revealed relatively high expression in HeLa cells and in a human retinal cell line, with lower levels in Jurkat T cells and in two B-cell lines. Interestingly, expression of MBP-1 mRNA was inducible by mitogen and phorbol ester treatment of Jurkat T cells and by serum treatment of confluent serum-deprived human fibroblasts.
先前从一个B细胞文库中分离出一个cDNA,它编码一种序列特异性DNA结合蛋白,该蛋白对I类主要组织相容性复合体(MHC)和κ免疫球蛋白基因增强子中的相关位点具有亲和力。我们在此报告MBP-1(MHC增强子结合蛋白1)cDNA约6.5千碱基的序列。MBP-1蛋白的分子量预计大于200,000。对MHC增强子序列TGGGGATTCCCCA具有高亲和力的DNA结合结构域定位于一个118个氨基酸的蛋白质片段,该片段包含两个Cys2-X12-His2类锌指。对MBP-1 mRNA表达的分析显示,HeLa细胞和一种人视网膜细胞系中表达相对较高,而在Jurkat T细胞和两种B细胞系中表达水平较低。有趣的是,用丝裂原和佛波酯处理Jurkat T细胞以及用血清处理汇合的血清饥饿的人成纤维细胞可诱导MBP-1 mRNA的表达。