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人类TATA结合蛋白基因的转录调控

Transcriptional regulation of the human TATA binding protein gene.

作者信息

Harland Lee, Crombie Robert, Anson Simon, deBoer Jasper, Ioannou Panayiotis A, Antoniou Michael

机构信息

Nuclear Biology Group, Division of Medical and Molecular Genetics, GKT School of Medicine, 8(th) Floor Guy's Tower, Guy's Hospital, London Bridge, London, SE1 9RT, UK.

出版信息

Genomics. 2002 Apr;79(4):479-82. doi: 10.1006/geno.2002.6728.

Abstract

The human TATA binding protein (TBP) locus consists of a functional domain of three closely linkedhousekeeping genes (TBP, PSMB1 (proteasomal C5 subunit), and PDCD2 (programmed cell death-2)) within a 50-kb interval at chromosome position 6q27. Here we demonstrate that a genomic clone spanning the 20-kb TBP gene, with 12 kb 5' and 3' flanking sequences, was fully functional in stable, transfected L-cells harboring a single copy of this transgene, including after long-term (60 day) culture in the absence of drug selective pressure. Furthermore, we were only able to detect DNaseI hypersensitive sites at the TBP and PSMB1 promoters present within this 44-kb fragment. Our data suggest that this 44-kb genomic region possesses genetic regulatory elements that not only drive ubiquitous expression of TBP but also negate chromatin and DNA methylation induced silencing, which is normally associated with transgenes stably integrated into tissue culture cells.

摘要

人类TATA结合蛋白(TBP)基因座由三个紧密相连的管家基因(TBP、PSMB1(蛋白酶体C5亚基)和PDCD2(程序性细胞死亡2))的功能域组成,位于6号染色体6q27位置的一个50 kb区间内。在此,我们证明了一个跨越20 kb TBP基因且带有12 kb 5'和3'侧翼序列的基因组克隆,在携带该转基因单拷贝的稳定转染L细胞中具有完全功能,包括在无药物选择压力的长期(60天)培养后。此外,我们仅能在这个44 kb片段内的TBP和PSMB1启动子处检测到DNaseI超敏位点。我们的数据表明,这个44 kb的基因组区域拥有遗传调控元件,这些元件不仅驱动TBP的普遍表达,还能消除通常与稳定整合到组织培养细胞中的转基因相关的染色质和DNA甲基化诱导的沉默。

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