Elevated levels of ribosomal proteins eL36 and eL42 control expression of Hsp90 in rhabdomyosarcoma

Sarah Shaikho, C. Dobson, Thet Naing, Bahram Samanfar, H. Moteshareie, Maryam Hajikarimloo, A. Golshani, M. Holcik
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引用次数: 5

Abstract

ABSTRACT Mammalian 90 kDa heat shock protein (Hsp90) is a ubiquitous molecular chaperone whose expression is selectively upregulated during stress, although the precise control mechanism of this increase is yet to be fully elucidated. We used polysome profiling to show that Hsp90α mRNA is selectively translated, while global translation is inhibited during heat stress. Furthermore, we have identified 2 ribosomal proteins, eL36 and eL42 that modulate Hsp90α expression under both normal and heat shock conditions. Importantly, we noted that expression of eL36 and eL42 is elevated in a panel of human rhabdomyosarcomas where it drives high expression of Hsp90 and modulates sensitivity of these cells to an Hsp90 inhibitor 17-AAG.
高水平的核糖体蛋白eL36和eL42控制横纹肌肉瘤Hsp90的表达
哺乳动物90kda热休克蛋白(Hsp90)是一种普遍存在的分子伴侣蛋白,其表达在应激状态下选择性上调,尽管这种上调的精确控制机制尚未完全阐明。我们使用多聚体分析来证明Hsp90α mRNA是选择性翻译的,而热应激时全局翻译被抑制。此外,我们还鉴定了两个核糖体蛋白eL36和eL42,它们在正常和热休克条件下都能调节Hsp90α的表达。重要的是,我们注意到eL36和eL42的表达在人横纹肌肉瘤中升高,它驱动Hsp90的高表达,并调节这些细胞对Hsp90抑制剂17-AAG的敏感性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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