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细胞内同源结构域蛋白SATB1和CDP与人类巨细胞病毒UL127基因和主要立即早期基因之间的独特区域结合。

Cellular homeoproteins, SATB1 and CDP, bind to the unique region between the human cytomegalovirus UL127 and major immediate-early genes.

作者信息

Lee Jialing, Klase Zachary, Gao Xiaoqi, Caldwell Jeremy S, Stinski Mark F, Kashanchi Fatah, Chao Sheng-Hao

机构信息

Expression Engineering Group, Bioprocessing Technology Institute, 20 Biopolis Way, #06-01 Centros, Singapore 138668, Singapore.

出版信息

Virology. 2007 Sep 15;366(1):117-25. doi: 10.1016/j.virol.2007.04.024. Epub 2007 May 18.

Abstract

An AT-rich region of the human cytomegalovirus (CMV) genome between the UL127 open reading frame and the major immediate-early (MIE) enhancer is referred to as the unique region (UR). It has been shown that the UR represses activation of transcription from the UL127 promoter and functions as a boundary between the divergent UL127 and MIE genes during human CMV infection [Angulo, A., Kerry, D., Huang, H., Borst, E.M., Razinsky, A., Wu, J., Hobom, U., Messerle, M., Ghazal, P., 2000. Identification of a boundary domain adjacent to the potent human cytomegalovirus enhancer that represses transcription of the divergent UL127 promoter. J. Virol. 74 (6), 2826-2839; Lundquist, C.A., Meier, J.L., Stinski, M.F., 1999. A strong negative transcriptional regulatory region between the human cytomegalovirus UL127 gene and the major immediate-early enhancer. J. Virol. 73 (11), 9039-9052]. A putative forkhead box-like (FOX-like) site, AAATCAATATT, was identified in the UR and found to play a key role in repression of the UL127 promoter in recombinant virus-infected cells [Lashmit, P.E., Lundquist, C.A., Meier, J.L., Stinski, M.F., 2004. Cellular repressor inhibits human cytomegalovirus transcription from the UL127 promoter. J. Virol. 78 (10), 5113-5123]. However, the cellular factors which associate with the UR and FOX-like region remain to be determined. We reported previously that pancreatic-duodenal homeobox factor-1 (PDX1) bound to a 45-bp element located within the UR [Chao, S.H., Harada, J.N., Hyndman, F., Gao, X., Nelson, C.G., Chanda, S.K., Caldwell, J.S., 2004. PDX1, a Cellular Homeoprotein, Binds to and Regulates the Activity of Human Cytomegalovirus Immediate Early Promoter. J. Biol. Chem. 279 (16), 16111-16120]. Here we demonstrate that two additional cellular homeoproteins, special AT-rich sequence binding protein 1 (SATB1) and CCAAT displacement protein (CDP), bind to the human CMV UR in vitro and in vivo. Furthermore, CDP is identified as a FOX-like binding protein and a repressor of the UL127 promoter, while SATB1 has no effect on UL127 expression. Since CDP is known as a transcription repressor and a nuclear matrix-associated region binding protein, CDP may have a role in the regulation of human CMV transcription.

摘要

人巨细胞病毒(CMV)基因组中位于UL127开放阅读框与主要立即早期(MIE)增强子之间的富含AT的区域被称为独特区域(UR)。研究表明,UR可抑制UL127启动子的转录激活,并在人CMV感染期间作为UL127和MIE这两个方向相反基因之间的边界发挥作用[安古洛,A.,克里,D.,黄,H.,博斯特,E.M.,拉津斯基,A.,吴,J.,霍博姆,U.,梅塞尔勒,M.,加扎尔,P.,2000年。鉴定与强效人巨细胞病毒增强子相邻的边界结构域,该结构域可抑制方向相反的UL127启动子的转录。《病毒学杂志》74(6),2826 - 2839;伦德奎斯特,C.A.,迈尔,J.L.,斯廷斯基,M.F.,1999年。人巨细胞病毒UL127基因与主要立即早期增强子之间的一个强负转录调控区域。《病毒学杂志》73(11),9039 - 9052]。在UR中鉴定出一个假定的叉头框样(FOX样)位点,AAATCAATATT,并发现其在重组病毒感染细胞中对UL127启动子的抑制中起关键作用[拉什米特,P.E.,伦德奎斯特,C.A.,迈尔,J.L.,斯廷斯基,M.F.,2004年。细胞抑制因子抑制人巨细胞病毒从UL127启动子的转录。《病毒学杂志》78(10),5113 - 5123]。然而,与UR和FOX样区域相关的细胞因子仍有待确定。我们之前报道过胰腺十二指肠同源盒因子1(PDX1)与位于UR内的一个45碱基对元件结合[赵,S.H.,原田,J.N.,海因德曼,F.,高,X.,纳尔逊,C.G.,钱达,S.K.,考德威尔,J.S.,2004年。PDX1,一种细胞同源结构域蛋白,与人巨细胞病毒立即早期启动子结合并调节其活性。《生物化学杂志》279(16),16111 - 16120]。在此我们证明,另外两种细胞同源结构域蛋白,富含特殊AT序列结合蛋白1(SATB1)和CCAAT置换蛋白(CDP),在体外和体内均可与人CMV的UR结合。此外,CDP被鉴定为一种FOX样结合蛋白和UL127启动子的抑制因子,而SATB1对UL127的表达没有影响。由于CDP是一种已知的转录抑制因子和核基质相关区域结合蛋白,CDP可能在人CMV转录调控中发挥作用。

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