核活性蛋白调节SRF辅因子MAL的动态亚细胞定位和活性
Maria K Vartiainen1, Sebastian Guettler, Banafshe Larijani
1Transcription Laboratory, Cancer Research UK, London Research Institute, Lincoln's Inn Fields Laboratories, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
概括
核活性蛋白通过控制MAL - - 血清反应因子 (SRF) 的联合激活剂来调节基因表达. 血清刺激触发了actin聚合,阻断了MAL核出口并激活了转录.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 转录条例 转录条例 转录条例
背景情况:
- 动氨酸主要被称为细胞骨蛋白.
- 乙烯酸还在调节基因表达方面发挥作用.
- 同激活剂MAL与活性蛋白和转录因子SRF相互作用.
研究的目的:
- 研究核活性蛋白在调节基因表达中的作用.
- 阐明MAL被actin控制的机制.
主要方法:
- 光共振能量转移 (FRET) 分析.
- MAL的细胞局部化研究.
- 对SRF目标基因活性的分析.
主要成果:
- 在未受刺激的细胞中,MAL在细胞质和细胞核之间穿.
- 血清刺激诱导了actin聚合,导致ALM在核中的积累.
- MAL-actin相互作用对于阻断核出口和使转录活动成为可能至关重要.
结论:
- 核活性蛋白作为一个信号枢纽,集成细胞外线索来调节转录调节.
- MAL-actin相互作用是SRF介导转录的关键调节点.
- 动氨酸聚合动态控制了像MAL这样的转录协活性剂的定位和活性.
相关概念视频
Regulation of Nuclear Protein Sorting
Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
Cell Polarization by Rho Proteins
Cell polarity is the asymmetric distribution of cellular and membrane components, making one side of the cell different from the other. This polarity is essential to many processes such as embryogenesis, axon migration, glucose transport across epithelial cells, and directional cell migration. A migrating cell responds to intracellular or extracellular signals via molecular cascades that reorganize the actin cytoskeleton to establish this polarity. In these cells, the Rho family proteins Cdc42,...
Protein Dynamics in Living Cells
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...


