非酵素的なRNA複製と互換性のある潜在的に前生物活性化化学
Stephanie J Zhang1, Daniel Duzdevich2, Jack W Szostak1,2
1Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, United States.
Journal of the American Chemical Society
|August 16, 2020
まとめ
この研究では,ブリッジ形成活性化を用いたリボ核酸 (RNA) 核酸の活性化のための新しい方法が導入されています. この進歩は 生命の起源を理解する上で 極めて重要な 非酵素型RNA複製を サポートしています
科学分野:
- 生命 研究 の 起源
- 前生物化学
- 分子 進化
背景:
- 非酵素リボ核酸 (RNA) 複製は,初期の遺伝情報の伝播のための提案されたメカニズムである.
- 継続的なRNA複製には,先行生物学的化学でこれまで解決されていない課題である核酸の活性化が必要です.
- シアノスルフィド化学は,プレバイオティックヌクレオチド活性化のための潜在的な経路を提供しているが,RNA複製との統合は証明されていない.
研究 の 目的:
- 非酵素複製と互換性のあるRNA核酸を活性化するための新しい経路を実証する.
- 継続的なRNA複製にプリバイオティックシアノスルフィド化学の適用を調査する.
- 早期のRNA伝播のより現実的なシミュレーションを可能にします.
主な方法:
- 新しい"ブリッジ形成活性化"経路の開発
- シアノスルフィド条件を用いたRNA核酸の化学活性化.
- 活性化ヌクレオチドを用いたテンプレート指向の非酵素RNA複製の実証
主要な成果:
- 新しい経路は,選択的に必要なイミダゾリウム・ブリッジド・ディヌクレオチドを生成する.
- 非酵素複製に適合する方法でRNA核酸の成功活性化.
- 核酸活性化による連続的なRNA複製の実証
結論:
- ブリッジ形成活性化は,継続的な非酵素RNA複製のための有効なメカニズムを提供します.
- この経路は前生物化学と 初期の遺伝物質の増殖の要件を結びつけています
- この発見により RNAベースの生命の起源の より正確なモデル化が容易になりました
関連する概念動画
Bacterial RNA Polymerase
32.1K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
32.1K
Bacterial RNA Polymerase
11.3K
11.3K
Bacterial Transcription
34.6K
RNA polymerase (RNAP) carries out DNA-dependent RNA synthesis in both bacteria and eukaryotes. Bacteria do not have a membrane-bound nucleus. So, transcription and translation occur simultaneously, on the same DNA template.
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
Transcription can be divided into three main stages, each involving distinct DNA sequences to guide the polymerase. These are:
34.6K
RNA Polymerase II Accessory Proteins
10.5K
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...
10.5K
Transcription Initiation
19.2K
Initiation is the first step of transcription in eukaryotes. Prokaryotic RNA Polymerase (RNAP) can bind to the template DNA and start transcribing. On the other hand, transcription in eukaryotes requires additional proteins, called transcription factors, to first bind to the promoter region in the DNA template. This binding helps recruit the specific RNAP that can assemble on the DNA and start transcription.
The promoters and enhancers and their accessory proteins allow tight regulation of...
The promoters and enhancers and their accessory proteins allow tight regulation of...
19.2K
Ribozymes
13.1K
The term ribozyme is used for RNA that can act as an enzyme. Ribozymes are mainly found in selected viruses, bacteria, plant organelles, and lower eukaryotes. Ribozymes were first discovered in 1982 when Tom Cech’s laboratory observed Group I introns acting as enzymes. This was shortly followed by the discovery of another ribozyme, Ribonulcease P, by Sid Altman’s laboratory. Both Cech and Altman received the Nobel Prize in chemistry in 1989 for their work on ribozymes.
Ribozymes can...
Ribozymes can...
13.1K


