丢失TDP-43诱导突触功能障碍,由UNC13A拼接切换ASOs进行挽救
Matthew J Keuss1, Peter Harley1, Eugeni Ryadnov1
1UCL Queen Square Motor Neuron Disease Centre and Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology, University College London; London, WC1N 3BG, UK.
bioRxiv : the preprint server for biology
|July 9, 2024
概括
失去TDP-43会导致UNC13A的拼接错误,这是与ALS和FTLD相关的基因. 用反感性寡核酸向这个错误恢复了UNC13A蛋白和突触功能,提供了一个潜在的治疗方法.
科学领域:
- 神经科学是一个神经科学.
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- TDP-43蛋白质功能障碍与ALS和FTLD等神经退行性疾病有关.
- UNC13A对突触传播至关重要,其基因是ALS/FTLD的风险因素.
研究的目的:
- 研究TDP-43损失对UNC13A拼接和突触功能的功能后果.
- 探索针对已确定拼接缺陷的治疗策略.
主要方法:
- 细胞或动物模型中的TDP-43耗尽.
- 对UNC13A拼接模式和蛋白质水平的分析.
- 电生理学记录以评估突触传输.
- 反感性寡核酸 (ASO) 处理以纠正拼接.
主要成果:
- 在UNC13A中,TDP-43的枯竭导致了神秘的外基因被纳入,导致了转录分解和蛋白质损失.
- 突触传输严重受损,以异步网络活动为特征.
- 针对密码外子的ASO疗法成功恢复了UNC13A蛋白水平和突触功能.
结论:
- 在UNC13A中,TDP-43依赖的密码表因子是TDP-43蛋白质病变中突触功能障碍的关键驱动因素.
- 通过ASOs准这个神秘的外显子,代表了对ALS和相关疾病的有希望的治疗途径.
相关概念视频
Nonsense-mediated mRNA Decay
10.6K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.6K
Alternative RNA Splicing
21.1K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
21.1K
RNA Splicing
56.3K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
56.3K
Regulation of the Unfolded Protein Response
2.4K
Inositol-requiring kinase one or IRE1 is the most conserved eukaryotic unfolded protein response (UPR) receptor. It is a type I transmembrane protein kinase receptor with a distinctive site-specific RNase activity. As the binding mechanics of the misfolded proteins with the N-terminal domain of IRE-1 are unclear, three binding models — direct, indirect, and allosteric -- are proposed for receptor activation. Nevertheless, it is known that once a misfolded protein associates with IRE1, it...
2.4K


