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Changes in the number of binding sites for ribonucleic acid polymerase in chromatin of WI-38 fibroblasts stimulated to proliferate

机译:刺激增殖的WI-38成纤维细胞染色质中核糖核酸聚合酶结合位点数目的变化

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p1. When WI-38 human diploid fibroblasts form confluent monolayers, DNA synthesis and cell division almost completely cease. A change of medium causes these density-inhibited cells to proliferate and within 1h after the application of the stimulus there is an increase in template activity of the chromatin isolated from stimulated cells. 2. The number of binding sites for iEscherichia coli/i RNA polymerase was determined on chromatin from WI-38 cells by two different methods, i.e. incorporation of [sup3/supH]UTP into RNA in the absence of reinitiation, and incorporation of [γ-sup32/supP]GTP into chain termini. 3. Both methods indicate that the capacity of chromatin to bind iE. coli/i RNA polymerase is increased in WI-38 cells stimulated to proliferate. 4. The increase in the number of binding sites for iE. coli/i RNA polymerase parallels the increase in chromatin template activity and suggests that the latter reflects an increase in the number of initiation sites, rather than an increase in the rate of transcription./p
机译:> 1。当WI-38人二倍体成纤维细胞形成融合单层时,DNA合成和细胞分裂几乎完全停止。更换培养基会导致这些抑制密度的细胞增殖,并且在施加刺激后1小时内,从刺激细胞中分离的染色质的模板活性会增加。 2.通过两种不同的方法,即将[ 3 H] UTP掺入RNA,测定WI-38细胞染色质上大肠埃希氏大肠杆菌RNA聚合酶的结合位点数目。在没有重新初始化的情况下,并将[γ- 32 P] GTP掺入链末端。 3.两种方法均表明染色质结合E的能力。刺激增殖的WI-38细胞中大肠杆菌RNA聚合酶增加。 4. E的结合位点数量增加。大肠杆菌RNA聚合酶与染色质模板活性的增加平行,并表明后者反映了起始位点数量的增加,而不是转录速率的增加。

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