热休克蛋白70
基因敲除
激活剂(遗传学)
荧光素酶
生物
高铁F1
热休克蛋白
基因表达
细胞生物学
基因
分子生物学
报告基因
生物化学
转染
作者
Youhei Saito,Takanobu Nakagawa,Ayana Kakihana,Yoshia Nakamura,Tomomi Nabika,Michihiro Kasai,Mai Takamori,Nobuyuki Yamagishi,Takahisa Kuga,Takumi Hatayama,Yuji Nakayama
摘要
The mammalian stress protein Hsp105β, which is specifically expressed during mild heat shock and localizes to the nucleus, induces the major stress protein Hsp70. In the present study, we performed yeast two-hybrid and one-hybrid screenings to identify the regulators of Hsp105β-mediated hsp70 gene expression. Six and two proteins were detected as Hsp105β- and hsp70 promoter-binding proteins, respectively. A luciferase reporter gene assay revealed that hsp70 promoter activation is enhanced by the transcriptional co-activator AF9 and splicing mediator SNRPE, but suppressed by the coiled-coil domain-containing protein CCDC127. Of these proteins, the knockdown of SNRPE suppressed the expression of Hsp70 irrespective of the presence of Hsp105β, indicating that SNRPE essentially functions as a transcriptional activator of hsp70 gene expression. The overexpression of HSP70 in tumor cells has been associated with cell survival and drug resistance. We here identified novel regulators of Hsp70 expression in stress signaling and also provided important insights into Hsp70-targeted anti-cancer therapy. J. Cell. Biochem. 117: 2109-2117, 2016. © 2016 Wiley Periodicals, Inc.
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