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首页> 外文期刊>Antioxidants and redox signalling >Unconventional Splicing of XBP-1 mRNA in the Unfolded Protein Response.
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Unconventional Splicing of XBP-1 mRNA in the Unfolded Protein Response.

机译:XBP-1 mRNA在非折叠蛋白反应中的非常规剪接。

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摘要

Cytoplasmic splicing is one of the major regulatory mechanisms of the unfolded protein response (UPR). The molecular mechanism of cytoplasmic splicing is unique and completely different from that of conventional nuclear splicing. The mammalian substrate of cytoplasmic splicing is XBP1 pre-mRNA, which is converted to spliced mRNA in response to UPR, leading to the production of an active transcription factor [pXBP1(S)] responsible for UPR. Interestingly, XBP1 pre-mRNA is also translated into a functional protein [pXBP1(U)] that negatively regulates the UPR. Thus, mammalian cells can quickly adapt to a change in conditions in the endoplasmic reticulum by switching proteins encoded in the mRNA from a negative regulator to an activator. This elaborate system contributes to various cellular functions, including plasma cell differentiation, viral infections, and carcinogenesis. In this short review, I briefly summarize research on cytoplasmic splicing and focus on current hot topics.
机译:细胞质剪接是未折叠的蛋白质反应(UPR)的主要调节机制之一。细胞质剪接的分子机制是独特的,与常规核剪接的分子机制完全不同。胞质剪接的哺乳动物底物是XBP1 pre-mRNA,它响应UPR而转换为剪接的mRNA,从而导致产生负责UPR的活性转录因子[pXBP1(S)]。有趣的是,XBP1 pre-mRNA也被翻译成对UPR负调控的功能蛋白[pXBP1(U)]。因此,哺乳动物细胞可以通过将mRNA中编码的蛋白质从负调节剂切换为激活剂,来快速适应内质网条件的变化。这个精心设计的系统有助于各种细胞功能,包括浆细胞分化,病毒感染和致癌作用。在这篇简短的评论中,我简要总结了关于细胞质剪接的研究,并将重点放在当前的热门话题上。

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