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相关概念视频

Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

15.1K
Transposons make up a significant part of genomes of various organisms. Therefore, it is believed that transposition played a major evolutionary role in speciation by changing genome sizes and modifying gene expression patterns. For example, in bacteria, transposition can lead to conferring antibiotic resistance. Movement of transposable elements within the genetic pool of pathogenic bacteria can aid in transfer of antibiotic-resistant genetic elements. In eukaryotes, transposons can carry out...
15.1K
RNA Editing02:23

RNA Editing

8.8K
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...
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Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

5.9K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
5.9K
Proofreading01:31

Proofreading

6.1K
Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
6.1K
DNA-only Transposons02:57

DNA-only Transposons

14.3K
DNA-only transposons are called autonomous transposons since they code for the enzyme transposase that is required for the transposition mechanism. Insertion of transposons can alter gene functions in multiple ways. They can mutate the gene, alter gene expression by introducing a novel promoter or insulator sequence, introduce new splice sites, and change the mRNA transcripts produced, or remodel chromatin structure.
The donor site from where the transposon is excised is either degraded or...
14.3K
Mismatch Repair01:20

Mismatch Repair

4.7K
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...
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相关实验视频

Updated: May 21, 2025

A Nonsequencing Approach for the Rapid Detection of RNA Editing
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A Nonsequencing Approach for the Rapid Detection of RNA Editing

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使用协调转换反应编辑蛋白质

Yi Hua1, Nicholas E S Tay1, Xuanjia Ye1

  • 1Department of Chemistry, Princeton University, Princeton, NJ, USA.

Science (New York, N.Y.)
|April 3, 2025
PubMed
概括
此摘要是机器生成的。

这项研究引入了蛋白质转换,这是蛋白质工程的一种新方法. 它可以在本地折叠条件下直接替换内部蛋白质区域,扩大蛋白质半合成应用.

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CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.
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CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.

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Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
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A Nonsequencing Approach for the Rapid Detection of RNA Editing

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CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.
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CRISPR/Cas9 Editing of the C. elegans rbm-3.2 Gene using the dpy-10 Co-CRISPR Screening Marker and Assembled Ribonucleoprotein Complexes.

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Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
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Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms

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科学领域:

  • 生物化学
  • 分子生物学
  • 蛋白质工程

背景情况:

  • 通过聚结合的蛋白质工程是强大的,但需要最后一个折叠步骤.
  • 这种限制限制了能够进行蛋白质半合成的系统类型.

研究的目的:

  • 开发一种在单一操作中替换内部蛋白区域的方法.
  • 通过在原生蛋白折叠条件下进行编辑来扩大蛋白半合成的范围.

主要方法:

  • 开发了一种蛋白质转换系统,使用直角对的工程分裂.
  • 类似于DNA转换,这种方法调解蛋白质编辑.
  • 这项技术应用于各种系统, 包括折叠蛋白质复合体.

主要成果:

  • 在单个步骤中成功替换了目标蛋白的内部区域.
  • 有助于有效地将非编码元素引入蛋白质.
  • 证明了该方法对折叠蛋白质复合物的适用性.

结论:

  • 蛋白质转换为蛋白质工程提供了一种多功能方法.
  • 这种方法克服了传统的结合策略的局限性.
  • 显著扩大了蛋白质半合成和功能化的可能性.