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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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Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

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RNA Polymerase (RNAP) is conserved in all animals, with bacterial, archaeal, and eukaryotic RNAPs sharing significant sequence, structural, and functional similarities. Among the three eukaryotic RNAPs, RNA Polymerase II is most similar to bacterial RNAP in terms of both structural organization and folding topologies of the enzyme subunits. However, these similarities are not reflected in their mechanism of action.
All three eukaryotic RNAPs require specific transcription factors, of which the...
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RNA Stability01:53

RNA Stability

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Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
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Alternative RNA Splicing02:18

Alternative RNA Splicing

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Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
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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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Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

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Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
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相关实验视频

Updated: Feb 16, 2026

Author Spotlight: A Computational Pipeline for Analyzing Chimeric Noncoding RNA-Target RNA Interactions in High-Throughput Sequencing Data
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Author Spotlight: A Computational Pipeline for Analyzing Chimeric Noncoding RNA-Target RNA Interactions in High-Throughput Sequencing Data

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一个针对单细胞RNA测序技术的实用指南.

Giulia Moro1, Erich Brunner2, Konrad Basler2

  • 1Department of Molecular Life Sciences, University of Zurich, Zurich, Switzerland. giulia.moro2@uzh.ch.

Communications biology
|February 14, 2026
PubMed
概括
此摘要是机器生成的。

单细胞RNA测序 (scRNA-seq) 偏差限制了转录检测. 本综述详细介绍了这些局限性,并介绍了有针对性的测序解决方案,以改善研究人员的转录和区域识别.

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科学领域:

  • 分子生物学分子生物学
  • 基因组学就是基因组学.
  • 生物信息学是一种生物信息学.

背景情况:

  • 目前的单细胞RNA测序 (scRNA-seq) 方法只能检测到10-40%的细胞转录.
  • 现有的高通量scRNA-seq方法主要捕获未翻译的区域,失去内部转录细节.

研究的目的:

  • 概述scRNA-seq协议中限制转录和区域检测的偏差.
  • 审查有针对性的测序解决方案,以增强scRNA-seq数据.
  • 为选择适当的目标方法提供决策树.

主要方法:

  • 对scRNA-seq协议偏差的审查.
  • 基于协议步骤的目标测序解决方案的分类.
  • 为方法选择制定决策框架的开发.

主要成果:

  • 在scRNA-seq协议步骤中识别关键偏差.
  • 将目标测序方法分为五个类别.
  • 一个决策树的演示,以指导实验设计.

结论:

  • 有针对性的测序提供了克服scRNA-seq限制的解决方案.
  • 了解协议偏差对于选择最佳方法至关重要.
  • 决策树有助于研究人员在scRNA-seq研究中改进转录和区域检测.