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相关概念视频

Lagging Strand Synthesis01:59

Lagging Strand Synthesis

50.5K
During replication, the complementary strands in double-stranded DNA are synthesized at different rates. Replication first begins on the leading strand. Replication starts later, occurs more slowly, and proceeds discontinuously on the lagging strand.
There are several major differences between synthesis of the leading strand and synthesis of the lagging strand. 1) Leading strand synthesis happens in the direction of replication fork opening, whereas lagging strand synthesis happens in the...
50.5K
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

10.6K
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,...
10.6K
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

9.9K
Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
9.9K
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
Homologous Recombination02:31

Homologous Recombination

50.3K
The basic reaction of homologous recombination (HR) involves two chromatids that contain DNA sequences sharing a significant stretch of identity. One of these sequences uses a strand from another as a template to synthesize DNA in an enzyme-catalyzed reaction. The final product is a novel amalgamation of the two substrates. To ensure an accurate recombination of sequences, HR is restricted to the S and G2 phases of the cell cycle. At these stages, the DNA has been replicated already and the...
50.3K
Mismatch Repair01:20

Mismatch Repair

4.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
4.8K

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相关实验视频

Updated: Jun 16, 2025

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
09:04

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids

Published on: September 21, 2017

9.5K

通过一个切断的循环进行RNA导向的合成.

Meng Su1, Samuel J Roberts1, John D Sutherland1

  • 1MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge CB2 0QH, UK.

Nucleic acids research
|August 20, 2024
PubMed
概括

研究人员探索了早期生命的RNA模板氨基化,证明了序列性形成. N-保护可以防止不必要的键,但立体选择性仍然是这种翻译前体的挑战.

科学领域:

  • 生命的起源研究 生命的起源研究
  • RNA 生物化学 生物化学
  • 益生菌化学 益生菌化学

背景情况:

  • 控制转移RNA (tRNA) 的氨基化对核糖体翻译至关重要.
  • 早期生活可能涉及更简单的基于RNA的氨基酸激活和转移系统.

研究的目的:

  • 为了研究 RNA 模板机制的序列氨基酸形成.
  • 探索非酶性氨基酸转移在前生物场景中的潜力.

主要方法:

  • 使用了短RNA寡核酸和氨基酸混合无水化物.
  • 研究了对接受器RNA链进行顺序转移的暂时化.
  • 采用N-受保护的氨基酸以控制反应通路.

主要成果:

  • 证明了氨基酸残留的顺序转移到RNA突起的二醇.
  • 观察到氨基和基的形成.
  • N-保护成功地防止了过早的乙烯形成.
  • 在N-acyl-aminoacyl转移步骤中发现了立体选择性的缺乏.

结论:

  • RNA模板系统可以促进序列氨基酸的形成,模仿早期的翻译步骤.

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Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures
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Self-Assembly of Gamma-Modified Peptide Nucleic Acids into Complex Nanostructures in Organic Solvent Mixtures

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Chemical Triphosphorylation of Oligonucleotides
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Chemical Triphosphorylation of Oligonucleotides

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Last Updated: Jun 16, 2025

Sequence-specific and Selective Recognition of Double-stranded RNAs over Single-stranded RNAs by Chemically Modified Peptide Nucleic Acids
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Chemical Triphosphorylation of Oligonucleotides

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  • 在前生物化学中,N-保护提供了一种控制雌性化的策略.
  • N-acyl-aminoacyl转移的非刻板选择性凸显了早期合成的关键挑战.