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Ribozymes02:47

Ribozymes

12.5K
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...
12.5K
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

30.3K
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...
30.3K
Riboswitches01:56

Riboswitches

8.5K
Riboswitches are non-coding mRNA domains that regulate the transcription and translation of downstream genes without the help of proteins. Riboswitches bind directly to a metabolite and can form unique stem-loop or hairpin structures in response to the amount of the metabolite present. They have two distinct regions – a metabolite-binding aptamer and an expression platform.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
8.5K
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

3.3K
3.3K
Bacterial Transcription01:53

Bacterial Transcription

29.4K
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:
29.4K
Leaky Scanning02:28

Leaky Scanning

5.2K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.2K

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関連する実験動画

Updated: Sep 10, 2025

Chemical Triphosphorylation of Oligonucleotides
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Chemical Triphosphorylation of Oligonucleotides

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生成モデルを用いた自己複製リボ酵素の空間を探索

Camille N Lambert1, Vaitea Opuu1,2, Francesco Calvanese1,3

  • 1Laboratoire de Biophysique et Evolution, UMR CNRS-ESPCI 8231 Chimie Biologie Innovation, ESPCI Paris, Université PSL, Paris, France.

Nature communications
|August 22, 2025
PubMed
まとめ

この研究は生命の起源に関する理論にとって 極めて重要なRNAの自己複製を 探求しています 研究者は1039の自己複製リボ酵素を発見し アビオゲネシスの理解を広げました

さらに関連する動画

Substrate Generation for Endonucleases of CRISPR/Cas Systems
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Substrate Generation for Endonucleases of CRISPR/Cas Systems

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Reverse Genetics to Engineer Positive-Sense RNA Virus Variants
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Reverse Genetics to Engineer Positive-Sense RNA Virus Variants

Published on: June 9, 2022

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関連する実験動画

Last Updated: Sep 10, 2025

Chemical Triphosphorylation of Oligonucleotides
13:19

Chemical Triphosphorylation of Oligonucleotides

Published on: June 2, 2022

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Substrate Generation for Endonucleases of CRISPR/Cas Systems
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Substrate Generation for Endonucleases of CRISPR/Cas Systems

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Reverse Genetics to Engineer Positive-Sense RNA Virus Variants
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Reverse Genetics to Engineer Positive-Sense RNA Virus Variants

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科学分野:

  • 生命 研究 の 起源
  • 分子生物学
  • 生物化学

背景:

  • RNAの自己複製はアビオゲネシスを理解する鍵です
  • この特性を示した触媒RNAは少ない.
  • RNA配列の探索は 生命の起源の研究に不可欠です

研究 の 目的:

  • 参考リボ酵素の多様化における生成力のモデルを比較する.
  • 高通量配列を用いてモデルの予測を実験的にテストする.
  • アビオゲネシスにおけるRNAの自己複製の可能性を定量的に評価する.

主な方法:

  • 統計的共変数と二次構造予測がRNA多様化のモデルに使用された.
  • 高通量シーケンシングは,モデル予測を実験的に検証するために使用されました.
  • 統計物理学の方法を使用して,自己複製リボ酵素の数を計算した.

主要な成果:

  • 10^39以上の自己触媒的自己複製を可能にするリボ酵素が計算された.
  • オリジナルから最大65の変異と99の変異のシーケンスが特定されました.
  • これはRNA配列の宇宙探査に 大きな可能性を秘めています

結論:

  • RNA 配列空間を探索するための効率的な方法が示されました.
  • 自己複製RNAに関する定量的なデータが提供された.
  • この発見は,アビオゲネシスの潜在的な経路を明らかにしています.