AMPD2 调节 GTP 合成,并发生突变成为一种可能可治疗的神经退行性脑干疾病
Naiara Akizu1, Vincent Cantagrel, Jana Schroth
1Neurogenetics Laboratory, Institute for Genomic Medicine, Rady Children's Hospital, Howard Hughes Medical Institute, University of California, San Diego, La Jolla, CA 92093, USA.
Cell
|August 6, 2013
概括
腺单酸脱氨酶2基因 (AMPD2) 的突变会导致神经退行性疾病. 这种状况的特征是点脑小细胞低成形 (PCH),可以通过补充纯素前体来治疗.
科学领域:
- 生物化学 生物化学
- 遗传学 是一个遗传学.
- 神经科学是一个神经科学.
背景情况:
- 纯素生物合成对于细胞能量和核酸合成至关重要.
- 新生合成受到腺和关氨酸核酸的严格调节.
- 在AMPD2的突变导致一个神经退行性状况,带有点脑小细胞低成形 (PCH).
研究的目的:
- 调查AMPD2在纯素代谢和神经退行症中的作用.
- 了解与AMPD2相关的PCH背后的分子机制.
- 探索AMPD2相关的PCH的潜在治疗策略.
主要方法:
- 早期发病的神经退行症患者的遗传分析.
- 生物化学试验以评估AMPD2在纯素代谢中的功能.
- 细胞和动物模型研究AMPD2缺乏的影响.
主要成果:
- 通过调节氨酸合成反,AMPD2对于维持氨酸核酸池至关重要.
- 缺少AMPD2会影响依赖GTP的蛋白质的翻译启动.
- 精氨酸前体的使用挽救了细胞模型中观察到的缺陷.
结论:
- AMPD2在氨酸代谢和神经发育中起着保留作用.
- 缺乏AMPD2会导致可治疗的脑小细胞缺血症 (PCH).
- 向精氨酸代谢为AMPD2相关的神经退行性疾病提供了潜在的治疗途径.
相关概念视频
GTPases and their Regulation
7.9K
Guanine nucleotide-binding proteins (G-proteins), also known as GTPases, are a superfamily of proteins that regulate many cellular processes, such as cell signaling, vesicular transport, and the regulation of cell shape and motility. Mutation or dysfunction of these proteins can lead to disease. There are around 40,000 known G-proteins that can broadly be classified into two groups ‒ small G-proteins consisting of a single domain and large multi-domain G-proteins.
Large G-proteins,...
Large G-proteins,...
7.9K
ATP Synthase: Mechanism
16.0K
In animals, the mitochondrial F1F0 ATP synthase is the key protein that synthesizes ATP molecules through a complex catalytic mechanism. While the nuclear genome encodes the majority of ATP synthase subunits, the mitochondrial genome encodes some of the enzyme's most critical components. The formation of this multi-subunit enzyme is a complex multi-step process regulated at the level of transcription, translation, and assembly. Defects in one or more of these steps can result in decreased...
16.0K
ATP Synthase: Structure
16.3K
ATP synthase or ATPase is among the most conserved proteins found in bacteria, mammals, and plants. This enzyme can catalyze a forward reaction in response to the electrochemical gradient, producing ATP from ADP and inorganic phosphate. ATP synthase can also work in a reverse direction by hydrolyzing ATP and generating an electrochemical gradient. Different forms of ATP synthases have evolved special features to meet the specific demands of the cell. Based on their specific feature, ATP...
16.3K
Activation and Inactivation of G Proteins
8.9K
Heterotrimeric G proteins are guanine nucleotide-binding proteins. As the name suggests, heterotrimeric G proteins are composed of three subunits: alpha, beta, and gamma. They remain GDP-bound or GTP-bound inside the cells and switch between inactive/active states. The Gα subunit possesses the nucleotide-binding pocket that binds guanine nucleotides and switches between GDP or GTP-bound states. In contrast, the Gꞵ and Gγ subunits are always bound together with high...
8.9K
GPCRs Regulate Adenylyl Cylase Activity
6.9K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
6.9K
Biosynthesis of Nucleic Acids
1.7K
Nucleic acid biosynthesis is a fundamental biochemical process that produces the purine and pyrimidine nucleotides essential for DNA and RNA synthesis. This pathway maintains a balanced nucleotide pool, preventing imbalances that could jeopardize genetic integrity and cellular function. Given the crucial role of nucleotides, their synthesis is tightly regulated to ensure proper cellular homeostasis.Purine BiosynthesisThe biosynthesis of purine nucleotides begins with ribose-5-phosphate, a...
1.7K


