The Effect of the aPKC Gene Encoding Atypical Protein Kinase C on the Lifespan of Drosophila melanogaster Depends on the Expression Level of Protein Kinase GSK3

被引:0
|
作者
Trostnikov, M. V. [1 ]
Veselkina, E. R. [1 ]
Andreev, Y. A. [1 ]
Khryachkova, A. Y. [1 ]
Roshina, N. V. [1 ,2 ]
Pasyukova, E. G. [1 ]
机构
[1] Kurchatov Inst, Inst Mol Genet, Natl Res Ctr, Moscow 123182, Russia
[2] Russian Acad Sci, Vavilov Inst Gen Genet, Moscow 119991, Russia
基金
俄罗斯基础研究基金会;
关键词
lifespan; nervous system; protein kinase aPKC; protein kinase GSK3; Drosophila melanogaster; GLYCOGEN-SYNTHASE KINASE-3; NEUROMUSCULAR-JUNCTION; POLARITY; GSK-3-BETA; SHAGGY; ESTABLISHMENT; GSK3-BETA; INTEGRITY; PAR-1; DEATH;
D O I
10.1134/S102279542301012X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Drosophila melanogastershaggy and aPKC genes encode highly conserved GSK3 (Glycogen Syntase Kinase 3) and aPKC (Protein Kinase C) protein kinases that play key roles in many cellular processes. We previously demonstrated that changes in shaggy expression in neurons affect lifespan. In this article, we show that changing the expression of the aPKC gene in neurons also affects lifespan. Changing the expression of the two protein kinases in all male or female neurons and in male motoneurons led to changes in lifespan, indicating that aPKC has no effect on GSK3 and GSK3 has a possible inhibitory effect on aPKC. At the same time, changes in the expression of two protein kinases in female motor neurons led to changes in lifespan, indicating the existence of a still unclear mechanism of interaction between these proteins. The elucidation of the mechanisms of interaction between aPKC, GSK3, and their other partners will deepen and expand our understanding of the causes of longevity and the ways to extend life.
引用
收藏
页码:18 / 29
页数:12
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