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相关概念视频

Ribozymes02:47

Ribozymes

11.2K
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...
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RNA Splicing01:32

RNA Splicing

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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...
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Experimental RNAi02:15

Experimental RNAi

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RNA interference (RNAi) is a cellular mechanism that inhibits gene expression by suppressing its transcription or activating the RNA degradation process. The mechanism was discovered by Andrew Fire and Craig Mello in 1998 in plants. Today, it is observed in almost all eukaryotes, including protozoa, flies, nematodes, insects, parasites, and mammals. This precise cellular mechanism of gene silencing has been developed into a technique that provides an efficient way to identify and determine the...
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RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

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Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
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相关实验视频

Updated: Jun 13, 2025

Use of Alu Element Containing Minigenes to Analyze Circular RNAs
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Use of Alu Element Containing Minigenes to Analyze Circular RNAs

Published on: March 10, 2020

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在体外自循环化方法基于自剪接的Ribozyme.

Kyung Hyun Lee1, Nan-Ee Lee1, Seong-Wook Lee1,2

  • 1R&D Center, Rznomics Inc., Seongnam 13486, Republic of Korea.

International journal of molecular sciences
|September 14, 2024
PubMed
概括
此摘要是机器生成的。

在体外循环RNA (circRNA) 制备方法对于生物医学应用至关重要,因为其增强了稳定性. 自剪接的 ribozymes 提供高效的 circRNA 生成,本综述详细介绍了 I 组和 II 组的 内子方法.

关键词:
对于RNA疗法来说,它是非常重要的.这是一种RNA疫苗.圆形的RNARNA是一个圆形的RNA.组I 内子 组I 内子第2组 内部 内部 内部里博酶里博酶是什么意思自己循环化的自我循环化.自动拼接的自己拼接.

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Large-scale Production of Recombinant RNAs on a Circular Scaffold Using a Viroid-derived System in Escherichia coli
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Large-scale Production of Recombinant RNAs on a Circular Scaffold Using a Viroid-derived System in Escherichia coli

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Chemical Triphosphorylation of Oligonucleotides
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相关实验视频

Last Updated: Jun 13, 2025

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科学领域:

  • 分子生物学分子生物学
  • 生物化学 生化学

背景情况:

  • 循环RNAs (circRNAs) 在生物医学应用中表现出比线性RNAs更高的稳定性和性能.
  • 在体外生成的circRNA对研究和治疗越来越重要.

研究的目的:

  • 审查和更新基于 ribozyme 的自剪接 in vitro circRNA 制剂的最新进展.
  • 讨论用于circRNA合成的不同 ribozyme 方法的优缺点.

主要方法:

  • 专注于自我拼接的 ribozymes,特别是 I 组和 II 组内子.
  • 总结了最近开发的自循环化技术,用于体外circRNA生成.

主要成果:

  • 自剪接的 ribozymes 提供了一个简单而有效的方法,用于 in vitro circRNA 生产.
  • 不同的 ribozyme 策略为特定应用提供了不同的优缺点.

结论:

  • 自剪接的 ribozymes 是一种关键的技术,用于产生高质量的 circRNAs 在体外.
  • 了解I组和II组内子方法的细微差别对于优化circRNA制备至关重要.