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相关概念视频

Initiation of Translation02:33

Initiation of Translation

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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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Improving Translational Accuracy02:07

Improving Translational Accuracy

11.9K
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...
11.9K
Leaky Scanning02:28

Leaky Scanning

5.2K
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
Transcription Elongation Factors02:35

Transcription Elongation Factors

11.2K
Transcription elongation is a dynamic process that alters depending upon the sequence heterogeneity of the DNA being transcribed. Hence, it is not surprising that the elongation complex's composition also varies along the way while transcribing a gene.
The transcription elongation is regulated via pausing of RNA polymerase on several occasions during transcription. In bacteria, these halts are necessary because the transcription of DNA into mRNA is coupled to the translation of that mRNA...
11.2K
Translation in Prokaryotes01:29

Translation in Prokaryotes

177
Prokaryote translation is a complex, highly coordinated process that converts genetic information from mRNA into functional proteins. It involves three stages: initiation, elongation, and termination, each facilitated by specific molecular components.Initiation of TranslationThe process begins with the assembly of the ribosomal subunits and initiation factors on the mRNA. In bacteria, the 30S ribosomal subunit recognizes the Shine-Dalgarno sequence in the mRNA, a conserved region upstream of...
177
Regulated mRNA Transport02:22

Regulated mRNA Transport

6.4K
In eukaryotes, transcription and translation are compartmentalized; an mRNA is first synthesized in the nucleus and then selectively transported to the cytoplasm for protein synthesis. Before transport, a pre-mRNA undergoes several steps of post-transcriptional modifications including splicing, 5' capping, and the addition of a poly-adenine tail. Various proteins bind to the pre-mRNA during these modifications. The mRNA transport takes place with the help of multiple proteins playing...
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相关实验视频

Updated: Sep 13, 2025

Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs
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Toeprinting Analysis of Translation Initiation Complex Formation on Mammalian mRNAs

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eIF1和eIF5动态控制翻译开始站点保真

Rosslyn Grosely1, Carlos Alvarado1, Ivaylo P Ivanov2

  • 1Dept. of Structural Biology, Stanford University School of Medicine, Stanford, CA, USA.

Nature structural & molecular biology
|July 28, 2025
PubMed
概括

人类翻译启动依赖于开始位置的识别. 这项研究揭示了启动因子eIF1和eIF5如何竞争控制启动地点的选择,确保准确的翻译并影响健康和疾病.

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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: Sep 13, 2025

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Monitoring eIF4F Assembly by Measuring eIF4E-eIF4G Interaction in Live Cells
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科学领域:

  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.
  • 生物化学 生物化学

背景情况:

  • 准确的翻译启动对于人类的蛋白质合成至关重要.
  • 虽然AUG是正规的起始编码子,但非AUG编码子也被识别,尽管效率较低.
  • 启动因子:真核细胞启动因子1 (eIF1) 和eIF5在开始地点的选择中起着关键作用,但它们的确切机制尚不清楚.

研究的目的:

  • 阐明eIF1和eIF5调节翻译开始地点选择的分子机制.
  • 了解这些因素如何区分正规的AUG和非AUG启动站点.
  • 揭示eIF1和eIF5在控制翻译准确度方面的动态相互作用.

主要方法:

  • 使用实时单分子测试.
  • 采用了体外复制的人体翻译系统.
  • 在人类细胞中证实了这一发现.

主要成果:

  • eIF1以两种不同的模式绑定启动复合体:在扫描期间稳定,在启动位置识别后暂时.
  • 需要eIF5结合才能终止eIF1重新结合,从而使转化能力强的核糖体形成.
  • 非AUG启动站改变了eIF1和eIF5的绑定动态,导致启动阻塞.

结论:

  • eIF1和eIF5直接竞争绑定到翻译启动复合体.
  • 它们的动态互动精确地调整了开始位置识别的保真度.
  • 这个过程的失调对人类健康和疾病有重大影响.