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相关概念视频

Eukaryotic RNA Polymerases00:58

Eukaryotic RNA Polymerases

26.8K
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...
26.8K
RNA Editing02:23

RNA Editing

9.8K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
9.8K
tRNA Activation02:26

tRNA Activation

22.6K
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...
22.6K
Bacterial RNA Polymerase00:43

Bacterial RNA Polymerase

32.5K
Unlike eukaryotes, bacteria use a single RNA Polymerase (RNAP) to transcribe all genes. The different subunits of bacterial RNAPhave distinct functions. The multisubunit structure of the bacterial RNAP helps the enzyme to maintain catalytic function, facilitate assembly, interact with DNA and RNA, and self-regulate its activity.
In most genes, the transcription site is a single base present upstream of the coding sequence. Though RNAP is a catalytically efficient enzyme, it does not recognize...
32.5K
Transfer RNA Synthesis02:36

Transfer RNA Synthesis

13.2K
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...
13.2K
Transcription Initiation01:47

Transcription Initiation

20.3K
Initiation is the first step of transcription in eukaryotes. Prokaryotic RNA Polymerase (RNAP) can bind to the template DNA and start transcribing. On the other hand, transcription in eukaryotes requires additional proteins, called transcription factors, to first bind to the promoter region in the DNA template. This binding helps recruit the specific RNAP that can assemble on the DNA and start transcription.
The promoters and enhancers and their accessory proteins allow tight regulation of...
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Rerouting reductant flux via protein tethering enhances biohydrogen production in Thermococcus kodakarensis.

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相关实验视频

Updated: Jan 16, 2026

Site Specific Lysine Acetylation of Histones for Nucleosome Reconstitution using Genetic Code Expansion in Escherichia coli
07:26

Site Specific Lysine Acetylation of Histones for Nucleosome Reconstitution using Genetic Code Expansion in Escherichia coli

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一个特定序列的RNA乙化催化剂.

Supuni Thalalla Gamage1, Shereen Howpay Manage1, Aldema Sas-Chen2

  • 1Chemical Biology Laboratory, National Cancer Institute, Frederick, MD, 21702, USA.

bioRxiv : the preprint server for biology
|October 1, 2025
PubMed
概括
此摘要是机器生成的。

研究人员描述了Thermococcus kodakarensis Nat10 (TkNat10),这是一个对古人类耐热性至关重要的酶. TkNat10乙化RNA,这种修饰对于生物体在高温时的适应性至关重要.

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Antibody-Free Assay for RNA Methyltransferase Activity Analysis
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A Facile Protocol to Generate Site-Specifically Acetylated Proteins in Escherichia Coli
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相关实验视频

Last Updated: Jan 16, 2026

Site Specific Lysine Acetylation of Histones for Nucleosome Reconstitution using Genetic Code Expansion in Escherichia coli
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Site Specific Lysine Acetylation of Histones for Nucleosome Reconstitution using Genetic Code Expansion in Escherichia coli

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Antibody-Free Assay for RNA Methyltransferase Activity Analysis
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A Facile Protocol to Generate Site-Specifically Acetylated Proteins in Escherichia Coli
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科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 考古研究 考古研究

背景情况:

  • N4-乙基丁 (ac4C) 是一种广泛传播的RNA修饰.
  • 丁乙转移酶催化了ac4C的结合.
  • 古代生物拥有独特的耐热机制.

研究的目的:

  • 在生物化学上描述Thermococcus kodakarensis Nat10 (TkNat10).
  • 调查TkNat10在古人类耐热性中的作用.
  • 定义TkNat10的基质特异性和辅因子要求.

主要方法:

  • 净化和生物化学测定TkNat10.
  • 使用多种基质进行RNA乙化试验.
  • 对TkNat10目标的全转录组分析.
  • 对于基质识别研究的高通量突变发生.

主要成果:

  • 在高温下,TkNat10对于T. kodakarensis的健康状况至关重要.
  • TkNat10表现出强大的,独立的活动,取决于温度,ATP和乙-CoA.
  • TkNat10优先修改具有5'-CCG-3'序列的非结构化RNA.
  • TkNat10可以被设计为利用非本土的乙-CoA捐赠者.

结论:

  • TkNat10的催化活性对于古人类的耐热性至关重要.
  • 对于TkNat10基质识别的已确定的序列和结构决定因素.
  • TkNat10作为研究ac4C修饰和RNA-蛋白相互作用的工具.