関連する実験動画
Updated: Jan 23, 2026

12:26
Optical Tweezers to Study RNA-Protein Interactions in Translation Regulation
Published on: February 12, 2022
5.7K
プログラム可能なRNA誘導型RNAエフェクタータンパク質
Simone Rauch1, Emily He2, Michael Srienc3
1Department of Chemistry, The University of Chicago, Chicago, Illinois, USA; Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, Illinois, USA.
Cell
|June 25, 2019
まとめ
研究者はCRISPR-CasにインスパイアされたRNAターゲティングシステム (CIRTS) を開発し,プログラム可能なRNA操作を行いました. この新しいシステムは 特定のトランスクリプトを標的とした様々なエフェクタータンパク質を 提供し 新しい治療戦略を提供します
科学分野:
- 分子生物学
- RNA 生物学
- 遺伝子規制
背景:
- エピトランスクリプトミックの調節は 細胞の情報流動に不可欠です
- 特定のRNAをエフェクタータンパク質で標的化することは限られており,研究と治療を妨げています.
研究 の 目的:
- 特定のRNA分子を標的とする新しいプログラム可能なシステムを開発する.
- RNAレベルで 細胞のプロセスを正確に操作できるように
主な方法:
- CRISPR-CasにインスパイアされたRNAターゲティングシステム (CIRTS) を作成するためのタンパク質エンジニアリング戦略.
- CIRTSが様々なエフェクタータンパク質 (核酶,分解機構,アクティベーター,塩基エディター) を供給する能力を実証する.
主要な成果:
- CIRTSはシンプルで一般化可能なRNAターゲティングアプローチです.
- CIRTSは既存のCRISPR-CasRNA結合システムよりも小さい.
- CIRTSはヒトのタンパク質成分を用いて作ることができる.
結論:
- CIRTSはRNAの調節過程を研究するための汎用的なプラットフォームを提供します.
- ヒト由来CIRTSは,表表写体調節療法において免疫反応を緩和する可能性があります.
関連する概念動画
RNA Polymerase II Accessory Proteins
10.8K
Proteins that regulate transcription can do so either via direct contact with RNA Polymerase or through indirect interactions facilitated by adaptors, mediators, histone-modifying proteins, and nucleosome remodelers. Direct interactions to activate transcription is seen in bacteria as well as in some eukaryotic genes. In these cases, upstream activation sequences are adjacent to the promoters, and the activator proteins interact directly with the transcriptional machinery. For example, in...
10.8K
RNA Interference
27.9K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
27.9K
Eukaryotic RNA Polymerases
26.8K
RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
All three eukaryotic RNAPs require specific transcription factors, of which the...
All three eukaryotic RNAPs require specific transcription factors, of which the...
26.8K
RNA Stability
35.6K
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...
35.6K
RNA Splicing
60.4K
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...
60.4K
RNA Editing
9.8K
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...
9.8K

