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Related Concept Videos

DNA-only Transposons02:57

DNA-only Transposons

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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...
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Overview of Transposition and Recombination02:13

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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...
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DNA as a Genetic Template02:05

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Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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DNA Topoisomerases02:02

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Topoisomerases are enzymes that relax overwound DNA molecules during various cell processes, including DNA replication and transcription. These enzymes regulate positive and negative DNA supercoiling without changing the nucleotide sequence. DNA overwinding in a clockwise direction results in positively supercoiled DNA, whereas underwinding in a counterclockwise direction produces negatively supercoiled DNA.
Types and Mechanism of action
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Conservative Site-specific Recombination and Phase Variation02:53

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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.
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Design and Synthesis of a Reconfigurable DNA Accordion Rack
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Reconfigurable T-junction DNA Origami.

Katherine G Young1, Behnam Najafi1, William M Sant2

  • 1Department of Physics, University of Oxford, Parks Road, Oxford, OX1 3PU, UK.

Angewandte Chemie (International Ed. in English)
|June 12, 2020
PubMed
Summary
This summary is machine-generated.

This study introduces a new DNA origami method for exploring DNA self-assembly mechanisms. This technique uses programmable DNA linkers and loops, enabling room-temperature assembly of nanostructures with simple interaction rules.

Keywords:
DNA nanotechnologyDNA origamiT-junctionsself-assembly

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Area of Science:

  • Nanotechnology
  • Molecular Biology
  • Biophysics

Background:

  • DNA self-assembly is a powerful technique for creating nanoscale structures and devices.
  • Current methods often rely on empirical design rules, limiting mechanistic understanding.
  • Exploring the fundamental mechanisms of DNA assembly is crucial for advancing the field.

Purpose of the Study:

  • To develop a DNA origami model system for investigating DNA self-assembly mechanisms.
  • To demonstrate a programmable approach to controlling DNA origami folding and assembly.
  • To explore the minimum requirements for successful DNA nanostructure formation.

Main Methods:

  • Utilized a DNA origami technique controlled by single-stranded loops within a DNA template.
  • Employed double-stranded DNA linkers to program pairwise interactions between loop sequences.
  • Assembly occurred via T-junctions formed by hybridization of linker overhangs with template loops.

Main Results:

  • Demonstrated that the DNA origami system allows for easy reconfiguration of template loops and linker interaction rules.
  • Showcased the assembly of simple T-junction origami motifs using only two interaction rules.
  • Confirmed that the assembly process can be effectively performed at room temperature.

Conclusions:

  • The developed DNA origami model system provides a versatile platform for studying DNA assembly mechanisms.
  • Programmable interactions through DNA linkers and loops offer precise control over nanostructure formation.
  • The ability to assemble structures with minimal rules at room temperature signifies a step towards more efficient DNA nanotechnology.