在Dictyostelium中的结尾是由cAMP依赖的蛋白激酶调节的
A J Harwood1, N A Hopper, M N Simon
1Imperial Cancer Research Fund, Clare Hall Laboratories, South Mimms, Herts, England.
Cell
|May 15, 1992
概括
在Dictyostelium discoideum前茎细胞中抑制循环AMP依赖蛋白激酶 (PKA) 延长了的迁移并阻止了茎细胞的分化. PKA活动对于调节细胞运动和在结尾期间的分化至关重要.
科学领域:
- 细胞和分子生物学 细胞和分子生物学
- 发育生物学 发展生物学
- 生物化学 生物化学
背景情况:
- 细胞分化和形态发生是通过信号通路调节的复杂过程.
- 迪西奥斯蒂 (Dictyostelium discoideum) 作为研究多细胞发育的模型生物.
- 循环AMP依赖蛋白激酶 (PKA) 在各种细胞过程中发挥作用,包括发育.
研究的目的:
- 为了研究PKA活动在前细胞分化和Dictyostelium discoideum的高潮中的作用.
- 确定PKA对于调节细胞运动和分化在高潮阶段的必要性.
主要方法:
- 一个特定的PKA抑制剂被置于Dictyostelium discoideum中一个前特异性促进物的控制之下.
- 在通常引发结尾的环境条件下观察到突变的.
- 进行了与野生类型细胞的共同开发测试.
- 通过DIF (差异化诱导因子),茎细胞形态原,评估了诱导性.
主要成果:
- 突变的牛表现出长期的迁移,而不是立即的高潮.
- 达到顶点,一旦启动,就会产生长长的结构,缺乏茎和子细胞.
- 突变细胞在与野生类型细胞共同发展时,向茎入口的迁移减少.
- 在突变细胞中,DIF的诱导性显著降低.
结论:
- 在结尾过程中,PKA活动对于预茎细胞的特征性细胞运动至关重要.
- 对于茎细胞的分化,PKA是必要的.
- 提出了一个模型,其中PKA调节的抑制器控制了DIF诱导的茎细胞分化,平衡迁移和结尾.
相关概念视频
Positive Regulator Molecules
100.8K
To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
100.8K
Positive Regulator Molecules
5.3K
Mitotic cell division results in daughter cells that exactly resemble the parent cell. However, errors in the DNA replication or distribution of genetic material may lead to genetic mutations that may be passed down to every new cell formed from the resulting abnormal cell. Propagation of such mutant cells is restricted through checkpoint mechanisms present at different stages of the cell cycle. These checkpoints involve regulator molecules that either promote or demote cell cycle events.
5.3K
Anaphase Promoting Complex
2.5K
The stepwise destruction of specific proteins is necessary for the progression and completion of the cell cycle. Such proteins are ubiquitinated by ubiquitin ligases and then subsequently destroyed by the proteasome. The SCF (Skp1/Cullin/F-box) and the anaphase-promoting complex (APC) are two important ubiquitin ligases involved in cell cycle progression. While SCF is active throughout the cell cycle, APC gets activated during metaphase to anaphase transition. Cdc20 or Cdh1 binds to APC and...
2.5K
cAMP-dependent Protein Kinase Pathways
7.3K
Cyclic Adenosine Monophosphate (cAMP) is an essential second messenger that activates protein kinase A (PKA) and regulates various biological processes. A single epinephrine molecule binds to GPCR and activates several heterotrimeric G proteins, each stimulating multiple adenylyl cyclase, amplifying the signal, and synthesizing large numbers of cAMP molecules. Small changes in cAMP concentration affect PKA activity. The binding of four cAMP molecules induces a conformational change in PKA,...
7.3K
IP3/DAG Signaling Pathway
12.5K
Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and...
12.5K
Calmodulin-dependent Signaling
5.0K
Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
5.0K


