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The effect of heat stress on frame switch splicing of X-box binding protein 1 gene in horse

机译:热应激对马X-box结合蛋白1基因框架开关剪接的影响

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摘要

ObjectiveAmong stress responses, the unfolded protein response (UPR) is a well-known mechanism related to endoplasmic reticulum (ER) stress. ER stress is induced by a variety of external and environmental factors such as starvation, ischemia, hypoxia, oxidative stress, and heat stress. Inositol requiring enzyme 1α (IRE1α)-X-box protein 1 (XBP1) is the most conserved pathway involved in the UPR and is the main component that mediates IRE1α signalling to downstream ER-associated degradation (ERAD)- or UPR-related genes. XBP1 is a transcription factor synthesised via a novel mechanism called ‘frame switch splicing’, and this process has not yet been studied in the horse XBP1 gene. Therefore, the aim of this study was to confirm the frame switch splicing of horse XBP1 and characterise its dynamics using Thoroughbred muscle cells exposed to heat stress.
机译:目的在应激反应中,未折叠蛋白反应(UPR)是与内质网(ER)应激相关的众所周知的机制。内质网应激是由多种外部和环境因素引起的,例如饥饿,局部缺血,缺氧,氧化应激和热应激。需要肌醇的酶1α(IRE1α)-X-box蛋白1(XBP1)是UPR中最保守的途径,并且是介导IRE1α信号传导下游ER相关降解(ERAD)或UPR相关基因的主要成分。 XBP1是一种通过称为“框架开关剪接”的新型机制合成的转录因子,目前尚未在马XBP1基因中研究此过程。因此,本研究的目的是确定马XBP1的帧切换剪接并使用暴露于热应激的纯种肌肉细胞表征其动态。

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