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人类ZFM1蛋白是一种转录抑制因子,它与阶段特异性激活蛋白的转录激活结构域相互作用。

Human ZFM1 protein is a transcriptional repressor that interacts with the transcription activation domain of stage-specific activator protein.

作者信息

Zhang D, Childs G

机构信息

Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

出版信息

J Biol Chem. 1998 Mar 20;273(12):6868-77. doi: 10.1074/jbc.273.12.6868.

Abstract

Stage-specific activator protein (SSAP) is the transcription factor responsible for the activation of the sea urchin late H1 gene at the mid-blastula stage of embryogenesis. SSAP contains an extremely potent transcription activation domain that functions 4-5-fold better than VP16 in a variety of mammalian cell lines. We used the two-hybrid screening technique to identify human cDNAs from an HL60 cell-derived cDNA library that encode proteins that interact with the transcription activation domain of SSAP. One of these cDNAs encodes ZFM1, a protein previously identified at the locus linked to multiple endocrine neoplasia type 1 (MEN1) and as presplicing factor SF1. Functional assays establish the ZFM1 protein as a transcriptional repressor. ZFM1 protein represses Gal4-GQC-mediated transcription, and this activity requires both a repression domain found in the N-terminal 137 amino acids of the protein, as well as a GQC interaction region. The physiological significance of repression mediated by ZFM1 comes from the ability of its specific repression domain to function when fused to Gal4 and tethered to promoters containing Gal4 binding sites. The activity is unique in that activated but not basal transcription levels are affected.

摘要

阶段特异性激活蛋白(SSAP)是一种转录因子,负责在胚胎发育的囊胚中期激活海胆晚期H1基因。SSAP包含一个极强的转录激活结构域,在多种哺乳动物细胞系中,其功能比VP16强4至5倍。我们利用双杂交筛选技术,从HL60细胞来源的cDNA文库中鉴定出编码与SSAP转录激活结构域相互作用的蛋白质的人类cDNA。其中一个cDNA编码ZFM1,该蛋白先前在与1型多发性内分泌肿瘤(MEN1)相关的位点被鉴定出来,并作为剪接前体因子SF1。功能分析确定ZFM1蛋白是一种转录抑制因子。ZFM1蛋白抑制Gal4 - GQC介导的转录,这种活性既需要该蛋白N端137个氨基酸中发现的抑制结构域,也需要一个GQC相互作用区域。ZFM1介导的抑制作用的生理意义在于,其特定的抑制结构域与Gal4融合并与含有Gal4结合位点的启动子相连时能够发挥作用。这种活性的独特之处在于它影响的是激活转录水平而非基础转录水平。

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