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相关概念视频

RNA Interference01:23

RNA Interference

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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...
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CRISPR/Cas9 Genome Editing01:28

CRISPR/Cas9 Genome Editing

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The CRISPR-Cas system serves as a bacterial defense mechanism against invading genetic elements such as viruses and plasmids, forming the foundation for its adaptation as a powerful genome-editing tool. Originally discovered in prokaryotes, this system has been repurposed to revolutionize genetic engineering across a wide range of organisms, including plants, animals, and humans. The core component, Cas9, is an endonuclease derived from Streptococcus pyogenes, capable of introducing...
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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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CRISPR and crRNAs02:53

CRISPR and crRNAs

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Bacteria and archaea are susceptible to viral infections just like eukaryotes; therefore, they have developed a unique adaptive immune system to protect themselves. Clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins (CRISPR-Cas) are present in more than 45% of known bacteria and 90% of known archaea.
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Types of RNA01:23

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Overview
Three main types of RNA are involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). These RNAs perform diverse functions and can be broadly classified as protein-coding or non-coding RNA. Non-coding RNAs play important roles in the regulation of gene expression in response to developmental and environmental changes. Non-coding RNAs in prokaryotes can be manipulated to develop more effective antibacterial drugs for human or animal use.
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Riboswitches01:56

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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.
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相关实验视频

Updated: Jul 11, 2025

CRISPR Guide RNA Cloning for Mammalian Systems
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工程CRISPR指导RNA用于可编程RNA传感器

Yang Liu1, Wei Liu1, Baojun Wang2,3

  • 1MRC Laboratory of Molecular Biology (LMB), Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, U.K.

Biochemical Society transactions
|November 13, 2023
PubMed
概括

克里斯普尔RNA传感器利用沃森-克里克基配对进行可编程RNA检测. 本综述阐明了基于CRISPR的RNA传感技术的指导RNA工程策略,局限性和未来应用.

关键词:
克里斯普尔是什么意思?克里斯普尔是什么意思?这是一个RNA传感器RNA传感器.在gRNARNA中.可以编程的可编程性.

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Dissection of Enhancer Function Using Multiplex CRISPR-based Enhancer Interference in Cell Lines
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Dual CRISPR-Interference Strategy for Targeting Synthetic Lethal Interactions Between Non-Coding RNAs in Cancer Cells
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Dual CRISPR-Interference Strategy for Targeting Synthetic Lethal Interactions Between Non-Coding RNAs in Cancer Cells

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相关实验视频

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科学领域:

  • 分子生物学分子生物学
  • 生物技术是生物技术.
  • 遗传学 是一个遗传学.

背景情况:

  • 克里斯普尔系统通过沃森-克里克基配对提供可编程RNA检测.
  • 这种机制将目标RNA与CRISPR效应器连接起来,以进行特定的检测.
  • RNA传感器是体内和体外应用的关键工具.

研究的目的:

  • 为工程CRISPR指导RNA (gRNA) 提供系统的概述,用于可编程RNA检测.
  • 为了澄清gRNA可编程性在当前基于CRISPR的RNA传感器中的作用.
  • 确定CRISPR启用RNA传感的局限性和未来方向.

主要方法:

  • 对基于CRISPR的RNA传感策略现有文献的审查.
  • 对设计CRISPR gRNA的不同方法的分析.
  • 评估CRISPRRNA检测中的可编程特性.

主要成果:

  • 克里斯普尔gRNA工程策略使可编程RNA检测成为可能.
  • gRNA的可编程性是CRISPRRNA传感器的特异性和多功能性的核心.
  • 已经开发出各种成功的RNA传感方法.

结论:

  • 基于CRISPR的RNA传感器代表了新功能和应用的一个有希望的领域.
  • 对CRISPR系统和gRNA工程的进一步了解将推动未来的发展.
  • 优化gRNA可编程性是克服CRISPRRNA传感当前局限性的关键.