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

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.

Keywords: Budding yeast; ER stress; HAC1; Non-conventional mRNA splicing; Unfolded protein response.

MeSH terms

  • Basic-Leucine Zipper Transcription Factors* / genetics
  • Basic-Leucine Zipper Transcription Factors* / metabolism
  • RNA Splicing
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Repressor Proteins* / genetics
  • Repressor Proteins* / metabolism
  • Saccharomyces cerevisiae Proteins* / genetics
  • Saccharomyces cerevisiae Proteins* / metabolism
  • Saccharomycetales* / genetics
  • Saccharomycetales* / metabolism
  • Unfolded Protein Response

Substances

  • Basic-Leucine Zipper Transcription Factors
  • HAC1 protein, S cerevisiae
  • RNA, Messenger
  • Repressor Proteins
  • Saccharomyces cerevisiae Proteins