相关实验视频
Updated: May 29, 2025

10:49
Measuring RAN Peptide Toxicity in C. elegans
Published on: April 30, 2020
6.6K
多氨酸通过稳定RNA的三级结构来增强来自CCUG重复的重复关联非AUG翻译
Akihiro Oguro1, Takeshi Uemura2, Kodai Machida3
1Division of Physical Fitness, Department of Molecular Physiology, The Jikei University School of Medicine, Tokyo, Japan.
The Journal of biological chemistry
|February 2, 2025
概括
多氨酸,特别是精氨酸,通过稳定RNA结构来促进CCUG重复的重复关联非AUG (RAN) 翻译. 这一发现揭示了重复膨胀障碍的分子机制.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 生物化学 生物化学
背景情况:
- 重复膨胀障碍是由异常的微卫星重复膨胀引起的.
- 重复关联的非AUG (RAN) 翻译是一种关键的致病机制,但其调节尚未完全理解.
- 多胺是重要的细胞胺,影响RNA-蛋白相互作用和细胞功能.
研究的目的:
- 研究聚胺在重复关联非AUG (RAN) 翻译中的作用.
- 探索聚氨酸与重复扩张障碍的致病机制之间的关系.
主要方法:
- 使用无细胞蛋白质合成系统和细胞培养.
- 评估CCUG重复RNA翻译在多氨酸的存在和缺乏的情况下.
- 进行了CCUG重复RNA的热稳定性分析.
主要成果:
- 多氨酸显著促进了CCUG重复RNA的RAN翻译.
- 聚胺枯竭抑制了CCUG-依赖的RAN转化,在聚胺添加后可以恢复.
- 精子在稳定CCUG重复RNA和增强RAN转化方面表现出最强的效果.
结论:
- 多氨酸通过稳定其三级结构来调节CCUG重复RNA RAN转化.
- 精子是CCUG重复RNA结构和RAN翻译的关键调节者.
- 这些发现为重复扩张障碍的分子基础和潜在的治疗点提供了洞察力.
相关概念视频
RNA Stability
33.2K
Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
33.2K
Chromatin Structure Regulates pre-mRNA Processing
6.9K
In eukaryotic cells, nascent mRNA transcripts need to undergo many post-transcriptional modifications to reach the cell cytoplasm and translate into functional proteins. For a long time, transcription and pre-mRNA processing were considered two independent events that occur sequentially in the cell. However, it has now been well established that transcription and pre-mRNA processing are two simultaneous processes that are precisely regulated inside the cell.
The chromatin structure, especially...
The chromatin structure, especially...
6.9K
Ribosomal RNA Synthesis
13.1K
Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
13.1K
Nonsense-mediated mRNA Decay
10.4K
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,...
10.4K
RNA Editing
8.9K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
8.9K
Nucleic Acid Structure
5.9K
The pentose sugar in DNA is deoxyribose, while in RNA the pentose sugar is ribose. The difference between the sugars is the presence of the hydroxyl group on the ribose's second carbon and a hydrogen on the deoxyribose's second carbon. The phosphate residue attaches to the hydroxyl group of the 5′ carbon of one sugar and the hydroxyl group of the 3′ carbon of the sugar of the next nucleotide, which forms a 5′ to 3′ phosphodiester linkage.
DNA Structure
DNA...
DNA Structure
DNA...
5.9K

