Yoshida Hiderou
Department of Biophysics, Graduate School of Science, Kyoto University, Kyoto, Japan., PRESTO-SORST, Japan Science and Technology Agency, Kyoto, Japan.
Antioxid Redox Signal. 2007 Dec;9(12):2323-33. doi: 10.1089/ars.2007.1800.
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.
细胞质剪接是未折叠蛋白反应(UPR)的主要调控机制之一。细胞质剪接的分子机制独特,与传统的核剪接完全不同。细胞质剪接的哺乳动物底物是XBP1前体mRNA,它在UPR的作用下转化为剪接后的mRNA,从而产生负责UPR的活性转录因子[pXBP1(S)]。有趣的是,XBP1前体mRNA也被翻译成一种功能性蛋白[pXBP1(U)],它对UPR起负调控作用。因此,哺乳动物细胞可以通过将mRNA中编码的蛋白从负调控因子切换为激活因子,快速适应内质网条件的变化。这个精细的系统有助于多种细胞功能,包括浆细胞分化、病毒感染和癌症发生。在这篇简短的综述中,我简要总结了关于细胞质剪接的研究,并重点关注当前的热点话题。