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人类SMARCE1r高迁移率族蛋白的特性分析

Characterization of human SMARCE1r high-mobility-group protein.

作者信息

Lee Young Mi, Shin Hyunjin, Choi Wonja, Ahn Sungmin, Kim Wankee

机构信息

Institute for Medical Sciences, Ajou University, Suwon 442-749, South Korea.

出版信息

Biochim Biophys Acta. 2002 Apr 12;1574(3):269-76. doi: 10.1016/s0167-4781(01)00373-6.

Abstract

The high-mobility-group (HMG) proteins are chromatin-associated proteins that are common to all higher organisms. They bind DNA in a sequence-specific or non-sequence-specific way to induce DNA bending, and regulate chromatin function and gene expression. Here we report the characterization of an HMG box-containing gene, designated human Smarce1r gene. It contained an open reading frame (ORF) encoding 317 amino acids and had 86% and 94% identity with the murine Smarce1r ORF at the nucleic acid and amino acid level, respectively. A putative nuclear localization signal, one HMG domain, and a coiled-coil domain were localized. A single transcript of 1.6 kb was ubiquitously expressed in various human tissues except for the fetal brain in which the transcript was barely detected. Western blot analysis revealed that human SMARCE1r was expressed in specific tissues such as colon and placenta. Subcellular fractionation, DNA-affinity column chromatography, and electrophoretic mobility shift assays showed that human SMARCE1r was associated with the nuclear matrix and that it possessed DNA binding activity, as expected.

摘要

高迁移率族(HMG)蛋白是所有高等生物共有的染色质相关蛋白。它们以序列特异性或非序列特异性方式结合DNA以诱导DNA弯曲,并调节染色质功能和基因表达。在此,我们报告了一个含HMG盒基因(命名为人类Smarce1r基因)的特征。它包含一个编码317个氨基酸的开放阅读框(ORF),在核酸和氨基酸水平上与小鼠Smarce1r ORF的同源性分别为86%和94%。定位了一个假定的核定位信号、一个HMG结构域和一个卷曲螺旋结构域。除了在胎儿脑中几乎检测不到该转录本外,1.6 kb的单一转录本在各种人体组织中广泛表达。蛋白质免疫印迹分析显示,人类SMARCE1r在结肠和胎盘等特定组织中表达。亚细胞分级分离、DNA亲和柱层析和电泳迁移率变动分析表明,人类SMARCE1r与核基质相关,并且如预期的那样具有DNA结合活性。

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