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Related Concept Videos

DNA Topoisomerases02:02

DNA Topoisomerases

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
Topoisomerases are divided into two main types.  Type I...
Translesion DNA Polymerases02:10

Translesion DNA Polymerases

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...
Overview of Transposition and Recombination02:13

Overview of Transposition and Recombination

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...
DNA-only Transposons02:57

DNA-only Transposons

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...
Transcription Attenuation in Prokaryotes02:42

Transcription Attenuation in Prokaryotes

Transcriptional attenuation occurs when RNA transcription is prematurely terminated due to the formation of a terminator mRNA hairpin structure.  Bacteria use these hairpins to regulate the transcription process and control the synthesis of several amino acids including histidine, lysine, threonine, and phenylalanine. Transcription attenuation takes place in the non-coding regions of mRNA.
There are several different mechanisms used to attenuate transcription. In ribosome mediated...
RNA Structure01:19

RNA Structure

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...

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Related Experiment Video

Updated: Jul 25, 2026

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling
08:04

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling

Published on: October 8, 2019

Tn7 recognizes transposition target structures associated with DNA replication using the DNA-binding protein TnsE.

J E Peters1, N L Craig

  • 1Howard Hughes Medical Institute, Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

Genes & Development
|March 29, 2001
PubMed
Summary

The bacterial transposon Tn7 uses the TnsE protein to target DNA replication sites for insertion. This process, guided by DNA binding, reveals insights into replication fork progression in bacteria.

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Last Updated: Jul 25, 2026

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling
08:04

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Published on: October 8, 2019

DNA-Tethered RNA Polymerase for Programmable In vitro Transcription and Molecular Computation
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Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity
04:04

Real-Time Quantification of the Effects of IS200/IS605 Family-Associated TnpB on Transposon Activity

Published on: January 20, 2023

Area of Science:

  • Molecular Biology
  • Genetics
  • Microbiology

Background:

  • Bacterial transposons are mobile genetic elements that can alter host genomes.
  • Transposon Tn7 utilizes the TnsE protein for site-specific integration.
  • Understanding Tn7's targeting mechanism is crucial for genetic engineering and microbial genetics.

Purpose of the Study:

  • To elucidate the mechanism by which the bacterial transposon Tn7 selects its insertion targets.
  • To investigate the role of the transposon-encoded DNA-binding protein TnsE in target recognition and transposition.
  • To determine how Tn7's insertion orientation relates to chromosomal DNA replication.

Main Methods:

  • Characterization of TnsE DNA-binding properties using wild-type and mutant proteins.
  • In vitro assays to assess TnsE interaction with various DNA structures.
  • Analysis of Tn7 insertion patterns around the Escherichia coli chromosome in vivo.

Main Results:

  • Tn7 transposition mediated by TnsE occurs with a specific orientation relative to DNA replication.
  • Mutant TnsE proteins with higher transposition activity exhibit enhanced DNA binding affinity.
  • TnsE preferentially interacts with specific DNA structures in vitro, guiding insertion.
  • Tn7 insertion patterns provide insights into DNA replication fork dynamics.

Conclusions:

  • The bacterial transposon Tn7 targets DNA replication machinery via the TnsE protein.
  • TnsE's DNA-binding affinity and specificity are critical for Tn7's site selection and orientation.
  • The study offers a model for how DNA replication influences transposon integration and provides insights into replication fork progression.