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相关概念视频

Transfer RNA Synthesis02:36

Transfer RNA Synthesis

11.9K
One of the unique features of tRNA is the presence of modified bases. In some tRNAs, modified bases account for nearly 20% of the total bases in the molecule. Altogether, these unusual bases protect the tRNA from enzymatic degradation by RNases.
Each of these chemical modifications is carried by a specific enzyme, post-transcription. All of these enzymes have unique base and site-specificity. Methylation, the most common chemical modification, is carried by at least nine different enzymes, with...
11.9K
Tail-anchoring of Proteins in the ER Membrane01:45

Tail-anchoring of Proteins in the ER Membrane

3.1K
Tail-anchored, or TA, proteins are estimated to make up to 3-5% of membrane proteins found in the eukaryotic cell. Such proteins have a single transmembrane domain located approximately 30 amino acid residues upstream from the C-terminal end. As a result, the signal recognition particle (SRP) cannot guide a TA protein to the ER membrane for cotranslational insertion. Hence, they are integrated into the ER membrane post-translationally using their C-terminal end as the anchor. TA proteins...
3.1K
tRNA Activation02:26

tRNA Activation

19.0K
Aminoacyl-tRNA synthetases are present in both eukaryotes and bacteria. Though eukaryotes have 20 different aminoacyl-tRNA synthetases to couple to 20 amino acids, many bacteria do not have genes for all of these aminoacyl-tRNA synthetases. Despite this, they still use all 20 amino acids to synthesize their proteins. For instance, some bacteria do not have the gene encoding the enzyme that couples glutamine with its partner tRNA. In these organisms, one enzyme adds glutamic acid to all of the...
19.0K
Leaky Scanning02:28

Leaky Scanning

5.1K
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...
5.1K
RNA Structure01:19

RNA Structure

4.7K
The basic structure of RNA consists of a string of ribonucleotides attached by phosphodiester bonds. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
There are three main types of ribonucleic acid (RNA) involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). All three...
4.7K
Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

23.7K
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...
23.7K

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相关实验视频

Updated: Jun 8, 2025

Analysis of RNA Processing Reactions Using Cell Free Systems: 3' End Cleavage of Pre-mRNA Substrates in vitro
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Analysis of RNA Processing Reactions Using Cell Free Systems: 3' End Cleavage of Pre-mRNA Substrates in vitro

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对人类ELAC2作为tRNA 3'处理酶的结构见解.

Chenyang Xue1,2, Junshan Tian1,2, Yanhong Chen3

  • 1Shenzhen Key Laboratory of Biomolecular Assembling and Regulation, School of Life Sciences, Southern University of Science and Technology, Shenzhen 518055 Guangdong, China.

Nucleic acids research
|November 4, 2024
PubMed
概括

人类elaC核糖核酶Z 2 (ELAC2) 酶的人类elaC核糖核酶Z 2 (ELAC2) 酶

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Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events
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Quantification of the Abundance and Charging Levels of Transfer RNAs in Escherichia coli
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Quantification of the Abundance and Charging Levels of Transfer RNAs in Escherichia coli

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相关实验视频

Last Updated: Jun 8, 2025

Analysis of RNA Processing Reactions Using Cell Free Systems: 3' End Cleavage of Pre-mRNA Substrates in vitro
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Analysis of RNA Processing Reactions Using Cell Free Systems: 3' End Cleavage of Pre-mRNA Substrates in vitro

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Artificial RNA Polymerase II Elongation Complexes for Dissecting Co-transcriptional RNA Processing Events
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Quantification of the Abundance and Charging Levels of Transfer RNAs in Escherichia coli
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科学领域:

  • 生物化学 生物化学
  • 结构生物学 结构生物学
  • 分子生物学分子生物学

背景情况:

  • 人类elaC核糖核酶Z 2 (ELAC2) 对于前体转移核糖核酸 (tRNA前) 处理至关重要.
  • ELAC2中的突变与前列腺癌和多变性心肌病相关.
  • 对于ELAC2的催化机制,人们对它的理解仍然不足.

研究的目的:

  • 阐明ELAC2在tRNA前结合和分裂活动的结构基础.
  • 了解ELAC2结构在疾病相关突变中的作用.

主要方法:

  • 低温电子显微镜 (cryo-EM) 用于确定人类ELAC2在apo,tRNA前结合和tRNA结合状态中的结构.
  • 生物化学测试分析疾病相关突变的影响.

主要成果:

  • 详细的结构揭示了ELAC2如何通过其灵活的臂域结合前tRNA.
  • 形状的变化,特别是C端螺旋,使3'拖车更容易进入活性部位.
  • 疾病相关突变的结构性影响的特征.

结论:

  • 该研究提供了对ELAC2在tRNA前处理中的机制的全面结构理解.
  • 这些发现提供了关于ELAC2突变如何促进疾病发展的见解.
  • 这项工作为未来针对ELAC2.2的治疗策略奠定了基础.