在小鼠雌激素受体中的类固醇结合和二元化活动的表征和局部化
S E Fawell1, J A Lees, R White
1Molecular Endocrinology Laboratory, Imperial Cancer Research Fund, Lincoln's Inn Fields, England.
Cell
|March 23, 1990
概括
鼠标雌激素受体中的一个特定区域对于DNA结合和二分化至关重要. 这一区域具有保存的疏水性重复,对核受体功能至关重要.
科学领域:
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
- 生物化学 生物化学
背景情况:
- 雌激素受体 (ERs) 是基因表达的关键调节者.
- 核受体构成了参与各种生物过程的超级家族.
- 蛋白质与蛋白质的相互作用和DNA结合对受体功能至关重要.
研究的目的:
- 为了确定小鼠雌激素受体内负责二分化和DNA结合的区域.
- 为了研究一个保存的疏水性七度重复在核受体功能中的作用.
主要方法:
- 鼠标雌激素受体的局部导向突变发生.
- 对受体二分化和DNA结合亲缘关系的分析.
- 对整个核受体超级家族中保存区域的序列分析.
主要成果:
- 类固醇结合域内的特定区域对于二分化和高亲和度DNA结合都至关重要.
- 在该地区确定了防水性残留物的一种保存的七度重复.
- 重复的N端半部分的突变破坏了二分化,而中心的突变取消了类固醇结合,表明重叠的域.
结论:
- 鉴定的区域及其保存的疏水性重复在雌激素受体功能中起着关键作用.
- 在雌激素受体内,类固醇结合和二元化域似乎重叠.
- 这些发现为核受体二分化和DNA结合的机制提供了洞察力.
更多相关视频
09:07Detecting the Ligand-binding Domain Dimerization Activity of Estrogen Receptor Alpha Using the Mammalian Two-Hybrid Assay
Published on: December 19, 2018
5.8K
08:02Visualization of Estrogen Receptors in Colons of Mice with TNBS-Induced Crohn's Disease using Immunofluorescence
Published on: March 12, 2020
6.1K
相关概念视频
Internal Receptors
57.4K
Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
57.4K
Types of Receptors: Internal Receptors
24.6K
Many cellular signals are hydrophilic and cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind intracellular receptors that reside within the cell cytoplasm or nucleus. Many mammalian steroid hormones and nitric oxide (NO) gas use this cell signaling mechanism.
Similar to membrane-bound receptors, the binding of a ligand to the intracellular receptor of causes a conformational change in the...
Similar to membrane-bound receptors, the binding of a ligand to the intracellular receptor of causes a conformational change in the...
24.6K
Transducer Mechanism: Nuclear Receptors
6.6K
Nuclear receptors, or NRs, are unique transcription factors that regulate gene transcription and affect the cellular pathways involved in reproduction, development, or metabolism. Their ability to be stimulated by small lipophilic ligands and control vital cellular processes makes them ideal drug targets. Nearly 10-15% of currently prescribed drugs target these receptors.
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
About 48 different soluble family members of nuclear receptors are identified that can be divided into two main classes:
6.6K
The Two-State Receptor Model
3.5K
The two-state receptor model explains a drug's interaction with receptors, such as G protein-coupled receptors and ligand-gated ion channels, to induce or inhibit a biological response. When no natural ligands are present, a receptor exists in an equilibrium of inactive (Ri) and active (Ra) conformations. The inactive form does not produce a response, while the active form generates a basal effect known as constitutive activity.
The binding affinity of a drug determines its interaction with...
The binding affinity of a drug determines its interaction with...
3.5K
