Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Overproduction of Sch9 leads to its aggregation and cell elongation in Saccharomyces cerevisiae. / Drozdova, Polina; Lipaeva, Polina; Рогоза, Татьяна; Zhouravleva, Galina; Bondarev, Stanislav.
в: PLoS ONE, Том 13, № 3, e0193726, 01.03.2018, стр. e0193726.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Overproduction of Sch9 leads to its aggregation and cell elongation in Saccharomyces cerevisiae
AU - Drozdova, Polina
AU - Lipaeva, Polina
AU - Рогоза, Татьяна
AU - Zhouravleva, Galina
AU - Bondarev, Stanislav
PY - 2018/3/1
Y1 - 2018/3/1
N2 - The Sch9 kinase of Saccharomyces cerevisiae is one of the major TOR pathway effectors and regulates diverse processes in the cell. Sch9 belongs to the AGC kinase family. In human, amplification of AGC kinase genes is connected with cancer. However, not much is known about the effects of Sch9 overproduction in yeast cells. To fill this gap, we developed a model system to monitor subcellular location and aggregation state of overproduced Sch9 or its regions fused to a fluorescent protein. With this system, we showed that Sch9-YFP forms detergent-resistant aggregates, and multiple protein regions are responsible for this. This finding corroborated the fact that Sch9-YFP is visualized as various fluorescent foci. In addition, we found that Sch9 overproduction caused cell elongation, and this effect was determined by its C-terminal region containing kinase domains. The constructs we present can be exploited to create superior yeast-based model systems to study processes behind kinase overproduction in cancers.
AB - The Sch9 kinase of Saccharomyces cerevisiae is one of the major TOR pathway effectors and regulates diverse processes in the cell. Sch9 belongs to the AGC kinase family. In human, amplification of AGC kinase genes is connected with cancer. However, not much is known about the effects of Sch9 overproduction in yeast cells. To fill this gap, we developed a model system to monitor subcellular location and aggregation state of overproduced Sch9 or its regions fused to a fluorescent protein. With this system, we showed that Sch9-YFP forms detergent-resistant aggregates, and multiple protein regions are responsible for this. This finding corroborated the fact that Sch9-YFP is visualized as various fluorescent foci. In addition, we found that Sch9 overproduction caused cell elongation, and this effect was determined by its C-terminal region containing kinase domains. The constructs we present can be exploited to create superior yeast-based model systems to study processes behind kinase overproduction in cancers.
KW - Gene Expression Regulation, Fungal
KW - Protein Aggregates
KW - Protein Domains
KW - Protein-Serine-Threonine Kinases/chemistry
KW - Saccharomyces cerevisiae/metabolism
KW - Saccharomyces cerevisiae Proteins/chemistry
KW - MULTIPLE-MYELOMA
KW - TARGET
KW - MECHANISM
KW - PRIONS
KW - SHUTTLE VECTORS
KW - PROTEIN-KINASES
KW - BREAST-CANCER
KW - YEAST
KW - GROWTH
KW - STRESS
UR - http://www.scopus.com/inward/record.url?scp=85042794021&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/overproduction-sch9-leads-aggregation-cell-elongation-saccharomyces-cerevisiae
U2 - 10.1371/journal.pone.0193726
DO - 10.1371/journal.pone.0193726
M3 - Article
C2 - 29494682
VL - 13
SP - e0193726
JO - PLoS ONE
JF - PLoS ONE
SN - 1932-6203
IS - 3
M1 - e0193726
ER -
ID: 36220387