Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

RNA Interference01:23

RNA Interference

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...
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...
Experimental RNAi02:15

Experimental RNAi

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...
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

[Research progress on the World Health Organization's priority pathogen list].

Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi·2025
Same author

[Research progress of chimeric antigen receptor T-cell therapy in the treatment of neuroblastoma].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2025
Same author

[Two cases of interstitial pneumonia with autoimmune features in children].

Zhonghua er ke za zhi = Chinese journal of pediatrics·2025
Same author

[A comprehensive review and future prospects of biobanking pathogenic microorganisms causing human infections in China].

Zhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]·2024
Same author

[Construction and application of standard system for the preservation of pathogenic microorganism resources].

Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi·2024
Same author

Effects of different mesh materials on complications after prophylactic placement for stoma formation: a systematic review and network meta-analysis.

Hernia : the journal of hernias and abdominal wall surgery·2024

相关实验视频

Updated: May 11, 2026

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
13:16

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA

Published on: January 22, 2018

作为随机降解PCR的RNAi:siRNA原料将mRNA转化为dRNAs,这些dRNAs被降解以产生新的siRNAs.

C Lipardi1, Q Wei, B M Paterson

  • 1Laboratory of Biochemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Cell
|November 10, 2001
PubMed
概括

短干扰RNAs (siRNAs) 通过向mRNA进行降解来启动RNA干扰 (RNAi). 这些siRNAs作为原始酶,通过RNA依赖RNA聚合酶 (RdRP) 活性将目标mRNA转化为双链RNA (dsRNA),从而产生新的siRNAs.

科学领域:

  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.
  • 在RNA生物学,RNA生物学.

背景情况:

  • 转录后基因沉默 (PTGS),抑制和RNA干扰 (RNAi) 涉及21-25个核酸RNA片段,这些片段来自双链RNA (dsRNA).
  • 短干扰RNAs (siRNAs) 是RNAi的关键介质,但它们的确切作用机制在很大程度上仍然未知.

研究的目的:

  • 阐明siRNAs调解RNA干扰和向mRNA降解的机制.
  • 研究蛋白质复合体在siRNA介导的基因沉默中的作用.
  • 为了确定负责dsRNA合成和siRNA生成的酶活性.

主要方法:

  • 从Drosophila胚胎提取物中分离siRNA-蛋白质复合体.
  • 在体外测定使用GFP和Pp-LucsiRNAs来评估mRNA降解.
  • 在目标mRNA转换实验中使用合成的21核酸GFP siRNA复合体.

主要成果:

  • 从Drosophila胚胎提取物中分离的siRNA直接向mRNA进行体外降解.
  • siRNAs,包括合成的 siRNAs,作为起始剂,将目标mRNA转化为dsRNA.
  • 这种dsRNA中间体被降解,在由RNA依赖RNA聚合酶 (RdRP) 活性介导的循环过程中产生新的siRNA.

更多相关视频

AQRNA-seq for Quantifying Small RNAs
05:12

AQRNA-seq for Quantifying Small RNAs

Published on: February 2, 2024

Isolation and Quantification of Axonal mRNAs Using Porous Membrane Inserts and RTddPCR
07:06

Isolation and Quantification of Axonal mRNAs Using Porous Membrane Inserts and RTddPCR

Published on: February 6, 2026

相关实验视频

Last Updated: May 11, 2026

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA
13:16

Assessment of DNA Contamination in RNA Samples Based on Ribosomal DNA

Published on: January 22, 2018

AQRNA-seq for Quantifying Small RNAs
05:12

AQRNA-seq for Quantifying Small RNAs

Published on: February 2, 2024

Isolation and Quantification of Axonal mRNAs Using Porous Membrane Inserts and RTddPCR
07:06

Isolation and Quantification of Axonal mRNAs Using Porous Membrane Inserts and RTddPCR

Published on: February 6, 2026

结论:

  • siRNAs通过一个依赖RdRP的机制直接准并将mRNA转化为dsRNA来启动RNAi.
  • 这一过程导致目标mRNA的降解和siRNA生产的放大,建立了一个自我维持的循环.
  • 这些发现揭示了一种新的mRNA沉默和drosophila中的siRNA生成机制.