Shaikho Sarah, Dobson Christine C, Naing Thet, Samanfar Bahram, Moteshareie Houman, Hajikarimloo Maryam, Golshani Ashkan, Holcik Martin
Molecular Biomedicine Program, Children's Hospital of Eastern Ontario Research Institute , Ottawa, Ontario, Canada.
Department of Biology and Ottawa Institute of Systems Biology, Carleton University , Ottawa, Ontario, Canada.
Translation (Austin). 2016 Oct 4;4(2):e1244395. doi: 10.1080/21690731.2016.1244395. eCollection 2016.
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.
哺乳动物90 kDa热休克蛋白(Hsp90)是一种普遍存在的分子伴侣,其表达在应激期间选择性上调,尽管这种增加的确切控制机制尚未完全阐明。我们使用多核糖体分析表明,Hsp90α mRNA在热应激期间被选择性翻译,而整体翻译受到抑制。此外,我们鉴定出2种核糖体蛋白,即eL36和eL42,它们在正常和热休克条件下均调节Hsp90α的表达。重要的是,我们注意到在一组人类横纹肌肉瘤中,eL36和eL42的表达升高,它们驱动Hsp90的高表达并调节这些细胞对Hsp90抑制剂17-AAG的敏感性。