Neuroserpin Inclusion Bodies in a FENIB Yeast Model.
Valentina VaporeCorrado MazzagliaDiego SibiliaMara Del VecchioGernot FruhmannMarta ValentiElena MirandaTeresa RinaldiJoris WinderickxCristina MazzoniPublished in: Microorganisms (2021)
FENIB (familial encephalopathy with neuroserpin inclusion bodies) is a human monogenic disease caused by point mutations in the SERPINI1 gene, characterized by the intracellular deposition of polymers of neuroserpin (NS), which leads to proteotoxicity and cell death. Despite the different cell and animal models developed thus far, the exact mechanism of cell toxicity elicited by NS polymers remains unclear. Here, we report that human wild-type NS and the polymerogenic variant G392E NS form protein aggregates mainly localized within the endoplasmic reticulum (ER) when expressed in the yeast S. cerevisiae. The expression of NS in yeast delayed the exit from the lag phase, suggesting that NS inclusions cause cellular stress. The cells also showed a higher resistance following mild oxidative stress treatments when compared to control cells. Furthermore, the expression of NS in a pro-apoptotic mutant strain-induced cell death during aging. Overall, these data recapitulate phenotypes observed in mammalian cells, thereby validating S. cerevisiae as a model for FENIB.
Keyphrases
- cell death
- dengue virus
- cell cycle arrest
- induced apoptosis
- oxidative stress
- endoplasmic reticulum
- endothelial cells
- wild type
- zika virus
- single cell
- early onset
- dna damage
- saccharomyces cerevisiae
- induced pluripotent stem cells
- diabetic rats
- anti inflammatory
- gene expression
- dna methylation
- aedes aegypti
- binding protein
- endoplasmic reticulum stress
- bone marrow
- amino acid
- cell proliferation
- pluripotent stem cells
- molecular dynamics
- copy number
- drug induced
- breast cancer cells