未折叠蛋白反应
RNA剪接
内质网
细胞生物学
信使核糖核酸
酿酒酵母
化学
生物
分子生物学
酵母
基因
遗传学
核糖核酸
作者
Weihan Li,Robert H. Singer
出处
期刊:Methods in molecular biology
日期:2022-01-01
卷期号:: 113-120
被引量:2
标识
DOI:10.1007/978-1-0716-1732-8_8
摘要
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.
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