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相关概念视频

piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

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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...
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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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siRNA - Small Interfering RNAs02:30

siRNA - Small Interfering RNAs

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Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
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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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Bacterial Transcription01:53

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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:
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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.
The aptamer has high specificity for a particular metabolite which allows riboswitches to specifically regulate...
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相关实验视频

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Enhanced Crosslinking Immunoprecipitation eCLIP Method for Efficient Identification of Protein-bound RNA in Mouse Testis
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目标RNA识别驱动PIWI复杂组件用于转子子沉默

Júlia Portell-Montserrat1, Laszlo Tirian2, Changwei Yu2

  • 1Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna BioCenter (VBC), Dr. Bohr-Gasse 3, 1030 Vienna, Austria; Institute of Molecular Pathology (IMP), Campus Vienna BioCenter, 1030 Vienna, Austria; Vienna BioCenter PhD Program, Doctoral School of the University of Vienna, Medical University of Vienna, Vienna, Austria.

Molecular cell
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概括

与PIWI相互作用的RNAs (piRNAs) 和PIWI蛋白通过形成PIWI*复合体来沉默转子. 这些复合体作为招募下游效应者的平台,确保基因组完整性.

关键词:
阿尔戈纳特蛋白类植物通过PIWI-piRNA途径细菌系生物学异染色体的生物学皮RNA生物发生蛋白质结构预测小RNA路径转位子静音装置

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PAR-CliP - A Method to Identify Transcriptome-wide the Binding Sites of RNA Binding Proteins
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Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing RIPiT-Seq
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相关实验视频

Last Updated: Sep 8, 2025

Enhanced Crosslinking Immunoprecipitation eCLIP Method for Efficient Identification of Protein-bound RNA in Mouse Testis
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PAR-CliP - A Method to Identify Transcriptome-wide the Binding Sites of RNA Binding Proteins
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Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing RIPiT-Seq
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科学领域:

  • 分子生物学
  • 遗传学
  • 表观遗传学

背景情况:

  • 通过沉默可移植元素,PIWI蛋白和piRNA对基因组稳定性至关重要.
  • 沉默通过不同的核和细胞质路径发生,涉及异色素蛋白的形成和RNA裂变.

研究的目的:

  • 阐明PIWI介导沉默的效应器招募机制.
  • 确定参与PIWI-piRNA指导目标识别的分子复合体.

主要方法:

  • 蛋白质-RNA相互作用的生物化学分析.
  • 在Drosophila melanogaster的体内研究.
  • 进化的比较分析.

主要成果:

  • 通过PIWI-piRNA复合体的向,形成PIWI*复合体,包括GTSF蛋白和Maelstrom.
  • 核PIWI*复合体使用SFiNX形成异色素.
  • 细胞质白复合体使用Spindle-E进行piRNA放大.

结论:

  • PIWI*复合体作为保护的分子平台,将目标识别与效应器招募联系起来.
  • 这种机制为PIWI介导的跨细胞区间的沉默提供了一个统一的原则.
  • 识别了一个保存的基因组防御机制.