首页> 外文期刊>The biochemical journal >Characterization of the interaction between the transcription factors human polyamine modulated factor (PMF-1) and NF-E2-related factor 2 (Nrf-2) in the transcriptional regulation of the spermidine/spermine N1-acetyltransferase (SSAT) gene
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Characterization of the interaction between the transcription factors human polyamine modulated factor (PMF-1) and NF-E2-related factor 2 (Nrf-2) in the transcriptional regulation of the spermidine/spermine N1-acetyltransferase (SSAT) gene

机译:转录因子人类多胺调节因子(PMF-1)与NF-E2相关因子2(Nrf-2)之间的相互作用在亚精胺/亚精胺N1-乙酰基转移酶(SSAT)基因的转录调控中的表征

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pPolyamines and polyamine analogues have been demonstrated to modulate the transcription of various genes. Spermidine/spermine iN/isup1/sup-acetyltransferase (SSAT) is transcriptionally regulated through the interaction of at least two itrans/i-acting transcription factors, NF-E2-related factor 2 (Nrf-2) and PMF-1 (polyamine modulated factor-1). Nrf-2has previously been shown to regulate transcription of other genes through interactions between its C-terminal leucine zipper and the leucine-zipper region of other members of the small Maf protein family (the term ‘Maf’ is derived from bm/busculoba/bponeurotic-bf/bibrosarcoma virus). Here it is demonstrated that the interaction between Nrf-2 and PMF-1 is mediated through the binding of the leucine-zipper region of Nrf-2 and a C-terminal coiled-coil region of PMF-1 that does not contain a leucine zipper. Mutations that interrupt either the leucine zipper of Nrf-2 or the coiled-coil region of PMF-1 are demonstrated to alter the ability of these factors to interact, thus their ability to regulate the transcription of the SSAT gene is lost./p
机译:已证明多胺和多胺类似物可调节各种基因的转录。亚精胺/亚精胺 N 1 -乙酰基转移酶(SSAT)通过至少两个反式作用转录因子NF-E2的相互作用进行转录调控相关因子2(Nrf-2)和PMF-1(多胺调节因子-1)。先前已显示Nrf-2通过其C末端亮氨酸拉链与小黑手党蛋白家族其他成员的亮氨酸拉链区之间的相互作用来调节其他基因的转录(术语“ Maf”源自 m < / b> usculo a poneurotic- f ibrosarcoma病毒)。在此证明,Nrf-2和PMF-1之间的相互作用是通过Nrf-2的亮氨酸拉链区和PMF-1的C末端卷曲螺旋区(不含亮氨酸拉链)的结合而介导的。突变中断了Nrf-2的亮氨酸拉链或PMF-1的卷曲螺旋区域,这些突变会改变这些因子相互作用的能力,从而失去调节SSAT基因转录的能力。

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