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相关概念视频

Improving Translational Accuracy02:07

Improving Translational Accuracy

11.6K
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...
11.6K
Initiation of Translation02:33

Initiation of Translation

24.7K
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...
24.7K
Leaky Scanning02:28

Leaky Scanning

4.5K
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...
4.5K
Post-translational Translocation of Proteins to the RER01:27

Post-translational Translocation of Proteins to the RER

5.6K
A sizable fraction of proteins destined for ER are first synthesized in the cell cytosol and then transported across the ER membrane–a process called post-translational translocation. Similar to cotranslationally translocated proteins, these proteins also use the Sec translocon complex to enter the ER lumen.
Targeting proteins to the ER
Hsp40 and Hsp70 chaperone molecules bind the translated proteins in the cytosol to prevent their folding. The chaperone binding helps to keep the signal...
5.6K
Translation in Prokaryotes01:29

Translation in Prokaryotes

2.8K
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...
2.8K
Diversity of Protists I01:15

Diversity of Protists I

2.3K
Excavata is a diverse group of protists that includes both chemoorganotrophic and phototrophic species, with some thriving in anaerobic environments. Among the key groups within Excavata are diplomonads and parabasalids, which are flagellated protists that lack mitochondria and chloroplasts. These microorganisms typically inhabit anoxic environments, such as the intestines of animals, where they exist either symbiotically or as parasites, relying on fermentation for energy production. Some...
2.3K

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Guidelines for minimal reporting requirements, design and interpretation of experiments involving the use of eukaryotic dual gene expression reporters (MINDR).

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An evolutionarily conserved phosphoserine-arginine salt bridge in the interface between ribosomal proteins uS4 and uS5 regulates translational accuracy in Saccharomyces cerevisiae.

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相关实验视频

Updated: May 4, 2026

Xenopus laevis as a Model to Identify Translation Impairment
10:24

Xenopus laevis as a Model to Identify Translation Impairment

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移动的状动物:在euplotids中经常发生编程的翻译框架移动.

Lawrence A Klobutcher1, Philip J Farabaugh

  • 1Department of Biochemistry, University of Connecticut Health Center, Farmington, CT 06032, USA. klobutcher@nso2.uchc.edu

Cell
|January 16, 2003
PubMed
概括

编程的+1转换框架移动在Euplotes ciliates中很常见. 这种高频率可能与它们独特的停止密码重新分配有关,影响遗传代码演变.

科学领域:

  • 分子生物学分子生物学
  • 遗传学 是一个遗传学.
  • 进化生物学 进化生物学

背景情况:

  • 类动物,特别是Euplotes属,表现出独特的遗传特征.
  • 翻译框架转移是一种已知的影响基因表达的生物机制.

研究的目的:

  • 调查Euplotes中编程+1转换移的频率.
  • 为了探索框架转移和阻止这个属中的子重新分配之间的潜在联系.

主要方法:

  • 对Euplotes物种的基因组和转录组数据的分析.
  • 生物信息学方法用于识别和量化框架转移事件.
  • 与其他状动物物种进行比较分析.

主要成果:

  • 有证据表明,Euplotes中编程+1转化移的发生率很高.
  • 频繁的移和停止子重新分配的发生之间的相关性.

结论:

  • 编程的+1框架转移是Euplotes基因表达的一个重要特征.
  • 停止编码子重新分配可能会加强Euplotes中频繁的移的演变.

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