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相关概念视频

Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

10.7K
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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Translation01:31

Translation

15.0K
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
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Leaky Scanning02:28

Leaky Scanning

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During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.2K
Termination of Translation01:44

Termination of Translation

25.6K
The large ribosomal subunit has several important structures essential to translation. These include the peptidyl transferase center (PTC) - which is the site where the peptide bond is formed - and a large, internal, water-filled tube through which the nascent polypeptide moves. This latter structure is called the Peptide Exit Tunnel, and it begins at the PTC and spans the body of the large ribosomal subunit. During translation, as the nascent polypeptide chain is synthesized, it passes through...
25.6K
Improving Translational Accuracy02:07

Improving Translational Accuracy

11.7K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.7K
Initiation of Translation02:33

Initiation of Translation

34.3K
Initiating translation is complex because it involves multiple molecules. Initiator tRNA, ribosomal subunits, and eukaryotic initiation factors (eIFs) are all required to assemble on the initiation codon of mRNA. This process consists of several steps that are mediated by different eIFs.
First, the initiator tRNA must be selected from the pool of elongator tRNAs by eukaryotic initiation factor 2 (eIF2). The initiator tRNA (Met-tRNAi) has conserved sequence elements including modified bases at...
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相关实验视频

Updated: Aug 3, 2025

Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems
06:18

Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems

Published on: April 26, 2019

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非编码翻译缓解

Jordan S Kesner1,2, Ziheng Chen1,2,3, Peiguo Shi1,2

  • 1Cardiometabolic Genomics Program, Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.

Nature
|April 12, 2023
PubMed
概括
此摘要是机器生成的。

从非编码DNA区域的翻译经常发生,特别是在癌症等疾病中. 这项研究揭示了一种涉及疏水性C终端尾巴的监控机制,该尾巴针对异常多的降解或膜局部化.

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De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
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De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data

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Xenopus laevis as a Model to Identify Translation Impairment
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Xenopus laevis as a Model to Identify Translation Impairment

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相关实验视频

Last Updated: Aug 3, 2025

Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems
06:18

Measurement of Specific Mycobacterial Mistranslation Rates with Gain-of-function Reporter Systems

Published on: April 26, 2019

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De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
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De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data

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Xenopus laevis as a Model to Identify Translation Impairment
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科学领域:

  • 遗传学
  • 分子生物学
  • 生物化学

背景情况:

  • 翻译发生在规范编码区域之外,包括长非编码RNA,未翻译区域和内子.
  • 这种非正规的转化与衰老,神经退化和癌症有关,许多瘤特异性抗原由此产生的.
  • 监测非编码转化和产生的多的功能演变的机制在很大程度上是未知的.

研究的目的:

  • 研究非编码翻译监控的机制.
  • 了解非编码区域中的多如何获得新的功能.
  • 阐明这些新型多的定位的生物化学途径.

主要方法:

  • 整合了超过1万个人类基因组和数百万个随机序列的大量并行分析.
  • 在全基因组的CRISPR屏幕上.
  • 进行深入的遗传和生化表征.

主要成果:

  • 在非编码基因组和遗传密码中的内在核酸偏差通常会产生具有疏水性C端尾的多.
  • BAG6膜蛋白分类复合物捕获这些疏水尾巴,引导聚进行降解或向膜.
  • 规范性蛋白质已经进化为缺乏C端的疏水残留物,使其与非编码转化产品区别开来.

结论:

  • 针对来自不同非编码基因组区域的不必要翻译存在安全监控机制.
  • 这种机制涉及BAG6复合体和疏水性C端尾部识别.
  • 确定了新进化的蛋白质偏好的膜定位的潜在生化途径.