首页> 外文期刊>Biological & pharmaceutical bulletin >Identification of active substances from Streptomyces culture fluids using p53-independent expression of p21/WAF1/Cip1 gene and their mode of action.
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Identification of active substances from Streptomyces culture fluids using p53-independent expression of p21/WAF1/Cip1 gene and their mode of action.

机译:使用不依赖p53的p21 / WAF1 / Cip1基因表达及其作用方式从链霉菌培养液中鉴定活性物质。

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摘要

An assay system was constructed to identify chemicals that have a potential to induce p21/WAF1 gene, a target of the tumor suppressor p53 critical for negative growth regulation. Screening of about 1300 culture fluids of Streptomyces resulted in identification of active substances which induced the p21 gene in a p53-independent manner; one was a mixture of four members of the actinomycin group, and the other was trichostatin A. Transcriptional regulatory regions of p21 gene for induction by actinomycin D and trichostatin A were determined by transient expression of luciferase constructs in cells which are p53-deficient (Saos-2) or express a mutated form of p53 (TMK-1). The essential transcriptional elements for the response to these drugs localize within 210 bp of the 5'-upstream region of human p21 gene, and Sp1 elements were determined to be critical for the induction. DNA-binding activity of Sp1 was not increased in cells treated with these drugs, but kinase inhibitors such as staurosporin and wortmannin inhibited the induction.
机译:构建了一个分析系统,以鉴定具有潜在诱导p21 / WAF1基因的化学物质,p21 / WAF1基因是抑制肿瘤生长的负向调控因子p53的靶标。筛选约1300种链霉菌培养液可鉴定出以p53非依赖性方式诱导p21基因的活性物质。一个是放线菌素组的四个成员的混合物,另一个是曲古抑菌素A。通过荧光素酶构建体在p53缺陷型(Saos)细胞中的瞬时表达来确定由放线菌素D和曲古抑菌素A诱导的p21基因的转录调控区域。 -2)或表达p53(TMK-1)的突变形式。对这些药物的反应所必需的转录元件位于人类p21基因5'上游区域的210 bp之内,并且确定Sp1元件对于诱导至关重要。在用这些药物处理的细胞中,Sp1的DNA结合活性没有增加,但是激酶抑制剂(如星形孢菌素和渥曼青霉素)抑制了诱导。

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