TY - JOUR

T1 - A set of Saccharomyces cerevisiae strains possessing [PSI+] prion formed by Sup35 protein with various deletions in prionogenic domain

AU - Куличихин, Константин Юрьевич

AU - Сопова, Юлия Викторовна

AU - Рубель, Александр Анатольевич

N1 - Conference code: 3

PY - 2023/12/4

Y1 - 2023/12/4

N2 - Amyloid aggregation is a key factor for the development of several lethal and incurable diseases, commonly named amyloidoses. The development of various pathologies might be caused by the aggregation of the same protein. This can be due to the ability of any particular protein to adopt several amyloid conformations, specific for the exact disease (Pick’s and Alzheimer’s disease-specific forms of tau protein). How the specific amyloid conformation is formed in each case is not fully understood.In yeast, translation termination factor Sup35 is one of the most extensively studied amyloidogenic proteins. Sup35 aggregation (induction of [PSI+] prion) inactivates the protein and leads to the suppression of nonsense-mutation as the result of read-through.Prionogenic domain of Sup35 protein (Sup35N) has several specific regions: N-terminal QN-rich region (QN), oligopeptide repeats (NR) and C-terminal region (CTN). Sup35 can form various strains of [PSI+] with predominant involvement of different regions of Sup35N into amyloid core thus mimicking disease-specific strains of amyloids described for human amyloidogenic proteins.We implemented the deletions of fragments encoding 1-39 a.a. (QN region) or 75-123/98-123 a.a. (CTN region) into SUP35 gene of yeast Saccharomyces cerevisiae. Then, we induced aggregation of Sup35 protein in the strains carrying mutated SUP35 gene and got the strains possessing [PSIΔ39+], [PSIΔ75-123+], or [PSIΔ98-123+] prion. A set of strains possessing [PSI+] formed by Sup35 protein with various deletions in Sup35N may be convenient model to study disease-specific strains of amyloids formed by human proteins.This research was funded by Russian Science Foundation (grant 20-14-00148-П) and by the St. Petersburg State University (project 94031363).

AB - Amyloid aggregation is a key factor for the development of several lethal and incurable diseases, commonly named amyloidoses. The development of various pathologies might be caused by the aggregation of the same protein. This can be due to the ability of any particular protein to adopt several amyloid conformations, specific for the exact disease (Pick’s and Alzheimer’s disease-specific forms of tau protein). How the specific amyloid conformation is formed in each case is not fully understood.In yeast, translation termination factor Sup35 is one of the most extensively studied amyloidogenic proteins. Sup35 aggregation (induction of [PSI+] prion) inactivates the protein and leads to the suppression of nonsense-mutation as the result of read-through.Prionogenic domain of Sup35 protein (Sup35N) has several specific regions: N-terminal QN-rich region (QN), oligopeptide repeats (NR) and C-terminal region (CTN). Sup35 can form various strains of [PSI+] with predominant involvement of different regions of Sup35N into amyloid core thus mimicking disease-specific strains of amyloids described for human amyloidogenic proteins.We implemented the deletions of fragments encoding 1-39 a.a. (QN region) or 75-123/98-123 a.a. (CTN region) into SUP35 gene of yeast Saccharomyces cerevisiae. Then, we induced aggregation of Sup35 protein in the strains carrying mutated SUP35 gene and got the strains possessing [PSIΔ39+], [PSIΔ75-123+], or [PSIΔ98-123+] prion. A set of strains possessing [PSI+] formed by Sup35 protein with various deletions in Sup35N may be convenient model to study disease-specific strains of amyloids formed by human proteins.This research was funded by Russian Science Foundation (grant 20-14-00148-П) and by the St. Petersburg State University (project 94031363).

KW - Saccharomyces cerevisiae

KW - Sup35

KW - deletion analysis

UR - https://www.mendeley.com/catalogue/2b0f48c4-f26c-3d39-8d49-446b6b544e75/

U2 - 10.17816/ecogen567848

DO - 10.17816/ecogen567848

M3 - тезисы

VL - 21

SP - 16

EP - 16

JO - ЭКОЛОГИЧЕСКАЯ ГЕНЕТИКА

JF - ЭКОЛОГИЧЕСКАЯ ГЕНЕТИКА

SN - 1811-0932

IS - 3

T2 - 3rd International Conference “Genetically modified organism. The Нistory, Achievements, Social and Environmental Risks”

Y2 - 3 October 2023 through 5 October 2023

ER -