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相关概念视频

Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

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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,...
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Mismatch Repair

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Overview
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DNA Topoisomerases02:02

DNA Topoisomerases

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Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
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Restarting Stalled Replication Forks02:37

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DNA replication is initiated at sites containing predefined DNA sequences known as origins of replication. DNA is unwound at these sites by the minichromosome maintenance (MCM) helicase and other factors such as Cdc45 and the associated GINS complex.The unwound single strands are protected by replication protein A (RPA) until DNA polymerase starts synthesizing DNA at the 5’ end of the strand in the same direction as the replication fork. To prevent the replication fork from falling apart,...
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RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
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相关实验视频

Updated: May 21, 2025

Nanomanipulation of Single RNA Molecules by Optical Tweezers
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Nanomanipulation of Single RNA Molecules by Optical Tweezers

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解结RNA:一种解决计算工件的方法.

Simón Poblete1,2, Mikolaj Mlynarczyk3, Marta Szachniuk3,4

  • 1Facultadde Ingeniería, Arquitectura y Diseño, Universidad San Sebastián, Santiago, Chile.

PLoS computational biology
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概括
此摘要是机器生成的。

这项研究引入了一个新的协议来解开复杂的RNA结构,解决常见的计算工件. 该方法有效地完善RNA模型,使其适合进一步分析.

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Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
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相关实验视频

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Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
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科学领域:

  • 计算生物学 计算生物学
  • 结构生物学 结构生物学
  • 生物物理学的生物物理.

背景情况:

  • RNA 3D 结构预测经常产生纠,这是复杂模型的计算工件.
  • 这些文物往往导致其他准确的RNA结构预测被排除在进一步研究之外.

研究的目的:

  • 介绍一种用于解决RNA3D模型中纠的新方案.
  • 在人工物移除过程中保护RNA模型的整体3D折叠和结构完整性.

主要方法:

  • 使用了SPQR粗粒度模型和短分子动力学模拟.
  • 实施的能源条款用于选择性修改,以在没有显著扭曲的情况下解开结构.

主要成果:

  • 在195个纠的RNA模型中成功解决了70%以上的交织和约40%的拉索.
  • 实现了81%的效率在解的形状被归类为文物,对原始几何最小的影响.
  • 在精细的RNA模型的ClashScore中表现出显著的改进.

结论:

  • 开发的协议提供了一种可行的方法来改进以前由于拓文物而被认为不适合的RNA模型.
  • 这种方法通过解决常见的计算问题来提高预测RNA结构的可用性.