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检测芽殖酵母中HAC1的非常规mRNA剪接和翻译激活

Detecting the Non-conventional mRNA Splicing and Translational Activation of HAC1 in Budding Yeast.

作者信息

Li Weihan, Singer Robert H

机构信息

Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

Methods Mol Biol. 2022;2378:113-120. doi: 10.1007/978-1-0716-1732-8_8.

Abstract

Protein-folding homeostasis in the endoplasmic reticulum (ER) is maintained by the unfolded protein response (UPR). UPR in Saccharomyces cerevisiae is regulated by a bZIP transcription factor, Hac1p. Under non-stress condition, HAC1 mRNA is translationally repressed. When un- or mis-folded proteins accumulate in the ER, HAC1 mRNA undergoes non-conventional mRNA splicing. The spliced HAC1 mRNA is translationally active and produces functional Hac1p, which initiates a transcriptional response that restores ER protein-folding homeostasis. Thus, the activation of yeast UPR is tightly regulated by HAC1 mRNA splicing. Here, we describe two methods that are used to monitor the splicing and translational status of HAC1 mRNA in budding yeast.

摘要

内质网(ER)中的蛋白质折叠稳态由未折叠蛋白反应(UPR)维持。酿酒酵母中的UPR由bZIP转录因子Hac1p调控。在非应激条件下,HAC1 mRNA的翻译受到抑制。当未折叠或错误折叠的蛋白质在内质网中积累时,HAC1 mRNA会进行非常规的mRNA剪接。剪接后的HAC1 mRNA具有翻译活性,并产生功能性的Hac1p,后者启动转录反应以恢复内质网蛋白质折叠稳态。因此,酵母UPR的激活受到HAC1 mRNA剪接的严格调控。在此,我们描述了两种用于监测芽殖酵母中HAC1 mRNA剪接和翻译状态的方法。

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