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盒状DNA:一种与胚胎癌细胞分化相关的新型调控元件。

BOX DNA: a novel regulatory element related to embryonal carcinoma cell differentiation.

作者信息

Kihara-Negishi F, Tsujita R, Negishi Y, Ariga H

机构信息

Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.

出版信息

Mol Cell Biol. 1993 Dec;13(12):7747-56. doi: 10.1128/mcb.13.12.7747-7756.1993.

Abstract

BOX DNA was previously isolated from the DNA sequence inserted in the enhancer B domain of mutant polyomavirus (fPyF9) DNA. We also reported that BOX DNA functioned negatively on DNA replication and transcription of another polyomavirus mutant (PyhrN2) in F9-28 cells, a subclone of mouse F9 embryonal carcinoma (EC) cells expressing the polyomavirus large T antigen. In this study, we demonstrate that BOX DNA enhances transcription from the thymidine kinase (TK) promoter in various EC cells. One or three copies of BOX DNA, linked to the bacterial chloramphenicol acetyltransferase gene under the control of the herpes simplex virus TK promoter, activated promoter activity in F9, P19, and ECA2 cells. Band shift assays using BOX DNA as a probe revealed that specific binding proteins were present in all EC cells examined; the patterns of BOX DNA-protein complexes were the same among them. A mutation introduced within BOX DNA abolished enhancer activity as well as the formation of specific DNA-protein complexes. In non-EC cells, including L and BALB/3T3 cells, the enhancer activity of BOX DNA on the TK promoter was not observed, although binding proteins specific to the sequence exist. In band shift assays, the patterns of the DNA-protein complexes of either L or BALB/3T3 cells were different from those of EC cells. Furthermore, the enhancer activity of BOX DNA decreased upon differentiation induction in all EC cells examined, of different origins and distinct differentiation ability. In parallel with the loss of enhancer activity, the binding proteins specific for BOX DNA decreased in these cells. Moreover, we cloned a genomic DNA of F9, termed BOXF1, containing BOX DNA sequence approximately 400 bp upstream from the RNA start site of the gene. BOXF1, containing a TATA-like motif and the binding elements for Sp1 and Oct in addition to BOX DNA, possessed promoter activity deduced by a BOXF1-chloramphenicol acetyltransferase construct. Deletion analyses of the construct revealed that the transcription of BOXF1 gene is regulated by BOX DNA, preferentially in undifferentiated EC cells versus differentiated cells. Hence, BOX DNA is probably a novel transcriptional element related to EC cell differentiation.

摘要

BOX DNA 先前是从插入突变多瘤病毒(fPyF9)DNA 增强子 B 结构域的 DNA 序列中分离出来的。我们还报道过,在表达多瘤病毒大 T 抗原的小鼠 F9 胚胎癌细胞的亚克隆 F9 - 28 细胞中,BOX DNA 对另一种多瘤病毒突变体(PyhrN2)的 DNA 复制和转录起负向作用。在本研究中,我们证明 BOX DNA 可增强多种胚胎癌细胞中胸苷激酶(TK)启动子的转录。与单纯疱疹病毒 TK 启动子控制下的细菌氯霉素乙酰转移酶基因相连的一份或三份 BOX DNA,激活了 F9、P19 和 ECA2 细胞中的启动子活性。用 BOX DNA 作为探针进行的凝胶迁移试验表明,在所检测的所有胚胎癌细胞中均存在特异性结合蛋白;它们之间的 BOX DNA - 蛋白质复合物模式相同。在 BOX DNA 内引入的一个突变消除了增强子活性以及特异性 DNA - 蛋白质复合物的形成。在包括 L 细胞和 BALB / 3T3 细胞在内的非胚胎癌细胞中,未观察到 BOX DNA 对 TK 启动子的增强子活性,尽管存在该序列的特异性结合蛋白。在凝胶迁移试验中,L 细胞或 BALB / 3T3 细胞的 DNA - 蛋白质复合物模式与胚胎癌细胞不同。此外,在所检测的所有不同来源和不同分化能力的胚胎癌细胞中,BOX DNA 的增强子活性在诱导分化后降低。与增强子活性丧失同时,这些细胞中对 BOX DNA 特异的结合蛋白减少。此外,我们克隆了 F9 的一个基因组 DNA,称为 BOXF1,它在该基因的 RNA 起始位点上游约 400 bp 处含有 BOX DNA 序列。BOXF1 除了含有 BOX DNA 外,还含有一个类似 TATA 的基序以及 Sp1 和 Oct 的结合元件,由一个 BOXF1 - 氯霉素乙酰转移酶构建体推断其具有启动子活性。对该构建体的缺失分析表明,BOXF1 基因的转录受 BOX DNA 调控,在未分化的胚胎癌细胞中比在分化细胞中调控更为优先。因此,BOX DNA 可能是一种与胚胎细胞分化相关的新型转录元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6fe/364846/ba69ba19ec57/molcellb00024-0560-a.jpg

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