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在伯基特淋巴瘤中,免疫球蛋白重链基因增强子对c-myc表达的失调需要一个与Myc相关的锌指蛋白相关因子结合位点。

A Myc-associated zinc finger protein-related factor binding site is required for the deregulation of c-myc expression by the immunoglobulin heavy chain gene enhancers in Burkitt's lymphoma.

作者信息

Hu Hsien-Ming, Arcinas Magdalena, Boxer Linda M

机构信息

Center for Molecular Biology in Medicine, Veterans Affairs Palo Alto Health Care System, Stanford University School of Medicine, Stanford, California 94305, USA.

出版信息

J Biol Chem. 2002 Mar 22;277(12):9819-24. doi: 10.1074/jbc.M111426200. Epub 2002 Jan 3.

Abstract

The deregulation of expression of the c-myc gene in Burkitt's lymphoma results from the translocation that links one c-myc allele to one of the immunoglobulin genes. This physical linkage promotes interactions between c-myc and immunoglobulin gene regulatory elements that affect c-myc transcription initiation and elongation. We have located a region in the c-myc promoter that is required for the complete activation by the immunoglobulin heavy chain gene enhancer. This regulatory element contains a core sequence, GGGAGG, similar to the GA box recognized by the transcription factor Myc-associated zinc finger protein (MAZ). UV cross-link analysis indicated that the mass of this protein did not correspond to that of MAZ, suggesting that a protein related to but distinct from MAZ bound to this site. Mutation of this regulatory element resulted in a loss of promoter activity induced by the immunoglobulin heavy chain gene enhancer. This site was also required for the c-myc promoter shift from P2 to P1. In vivo footprinting revealed that this site was occupied on the translocated c-myc allele but not on the untranslocated allele. Taken together, these findings suggest that this regulatory element is required for the full activation of c-myc promoter activity by the immunoglobulin heavy chain gene enhancer.

摘要

伯基特淋巴瘤中c-myc基因表达的失调是由一种易位导致的,这种易位将一个c-myc等位基因与一个免疫球蛋白基因连接在一起。这种物理连接促进了c-myc与免疫球蛋白基因调控元件之间的相互作用,从而影响c-myc转录的起始和延伸。我们在c-myc启动子中定位到了一个区域,该区域是免疫球蛋白重链基因增强子完全激活所必需的。这个调控元件包含一个核心序列GGGAGG,类似于转录因子Myc相关锌指蛋白(MAZ)识别的GA盒。紫外线交联分析表明,该蛋白的分子量与MAZ不符,这表明与MAZ相关但不同的一种蛋白结合到了这个位点。这个调控元件的突变导致免疫球蛋白重链基因增强子诱导的启动子活性丧失。这个位点对于c-myc启动子从P2向P1的转变也是必需的。体内足迹分析表明,这个位点在易位的c-myc等位基因上被占据,但在未易位的等位基因上未被占据。综上所述,这些发现表明这个调控元件是免疫球蛋白重链基因增强子完全激活c-myc启动子活性所必需的。

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