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利用p21/WAF1/Cip1基因的p53非依赖性表达从链霉菌培养液中鉴定活性物质及其作用方式。

Identification of active substances from Streptomyces culture fluids using p53-independent expression of p21/WAF1/Cip1 gene and their mode of action.

作者信息

Egawa K, Nishigori H, Kunimoto S, Takeuchi T, Nose K

机构信息

Department of Microbiology, Showa University School of Pharmaceutical Sciences, Tokyo, Japan.

出版信息

Biol Pharm Bull. 1998 Sep;21(9):899-904. doi: 10.1248/bpb.21.899.

Abstract

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.

摘要

构建了一种检测系统,用于鉴定有可能诱导p21/WAF1基因的化学物质,p21/WAF1基因是肿瘤抑制因子p53的一个靶点,对负生长调节至关重要。对约1300种链霉菌培养液进行筛选,结果鉴定出以p53非依赖方式诱导p21基因的活性物质;一种是放线菌素组四个成员的混合物,另一种是曲古抑菌素A。通过在p53缺陷型细胞(Saos-2)或表达p53突变形式的细胞(TMK-1)中瞬时表达荧光素酶构建体,确定了放线菌素D和曲古抑菌素A诱导p21基因的转录调控区域。对这些药物产生应答的必需转录元件定位于人p21基因5'上游区域的210 bp内,并且已确定Sp1元件对诱导至关重要。在用这些药物处理的细胞中,Sp1的DNA结合活性并未增加,但诸如星形孢菌素和渥曼青霉素等激酶抑制剂可抑制诱导作用。

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