Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele

中國醫藥大學機構典藏 China Medical University Repository, Taiwan > 台中附設醫院 > 期刊論文 > Item 310903500/30055

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題名:	Prenatal diagnosis of oculocutaneous albinism two mutations located at the same allele
作者:	Hsieh, YY;Wu, JY;Chang, CC;Tsai, FJ;Lee, CC;Tsai, HD;Tsai, CH
貢獻者:	附設醫院婦產部;China Med Coll Hosp, Dept Obstet & Gynecol, Taichung, Taiwan;China Med Coll Hosp, Dept Pediat & Med Genet, Taichung, Taiwan;China Med Coll Hosp, Dept Med Res, Taichung, Taiwan
日期:	2001
上傳時間:	2010-09-24 14:48:24 (UTC+8)
出版者:	JOHN WILEY & SONS LTD
摘要:	E2F-1 regulates the transcription of genes required for DNA synthesis. Previously, we have reported that UCN-01 suppresses E2F-1 protein expression without any noticeable effect on its mRNA level in gastric cancer cell line SK-GT5 (Clin. Cancer Res., 4: 2201-2206, 1998), In this study, we investigated the mechanism responsible for the suppression of E2F-1 expression by UCN-01 in SK-GT5 cells. After 24-h exposure to 1 muM UCN-01, E2F-1 protein expression was decreased by >99%, The suppressive effect of UCN-01 could be reversed by ubiquitin-dependent proteasome inhibitors such as calpain inhibitor I and lactacystin. Transfection experiments using expression plasmids encoding full-length E2F-1 or truncated E2F-1 with deletion of the COOH-terminal region (which is required for eliciting ubiquitination and protein degradation) revealed that the expression of truncated E2F-1 was not affected by UCN-01, Other cell-cycle-related and ubiquitin-proteasome-regulated proteins such as p21, p27, and cyclin B1 were not repressed by UCN-01 in E2F-1-overexpressing cells. In vitro-translated, full-length E2F-1 degraded more rapidly upon incubation with extracts from UCN-01-treated cells when compared with truncated E2F-1. Taken together, these data indicate that UCN-01 suppresses E2F-1 protein expression mediated by the ubiquitin-proteasome pathway in a specific manner.
關聯:	PRENATAL DIAGNOSIS 21(3):200-201
顯示於類別:	[台中附設醫院] 期刊論文

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