Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Insertion element IS102 resides in plasmid pSC101.

H Ohtsubo, M Zenilman, E Ohtsubo

    Journal of Bacteriology
    |October 1, 1980
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Clinical and ultrasound features of difficult-to-treat rheumatoid arthritis: A multicenter RA ultrasound cohort study.

    Scandinavian journal of rheumatology·2023
    Same author

    [Comparison of medical and social support system for children with severe disabilities in Toronto and Tokyo].

    No to hattatsu = Brain and development·2009
    Same author

    A new class of LINEs (ATLN-L) from Arabidopsis thaliana with extraordinary structural features.

    DNA research : an international journal for rapid publication of reports on genes and genomes·2002
    Same author

    Identification and structural analysis of SINE elements in the Arabidopsis thaliana genome.

    Genes & genetic systems·2001
    Same author

    Connectivity perception of partly occluded gratings in 4-month-old infants.

    Perception·2001
    Same author

    Structural and functional characterization of IS679 and IS66-family elements.

    Journal of bacteriology·2001

    Researchers discovered a novel 1-kilobase insertion sequence, IS102, during plasmid recombination studies. This sequence duplicated at recombination junctions and showed structural similarities to known mobile genetic elements.

    Area of Science:

    • Molecular Biology
    • Genetics
    • Microbiology

    Background:

    • Plasmid recombination is a key mechanism for genetic exchange in bacteria.
    • Understanding the molecular basis of recombination is crucial for microbial genetics.
    • Previous studies suggested that insertion sequences can mediate plasmid recombination.

    Purpose of the Study:

    • To investigate the mechanism of in vivo recombination between plasmid pHS1 and ColE1.
    • To characterize the structure and properties of recombinant plasmids.
    • To identify and define novel insertion sequences involved in recombination.

    Main Methods:

    • In vivo selection for tetracycline resistance at restrictive temperature.
    • Restriction endonuclease digestion and electron microscopy heteroduplex analysis.

    Related Experiment Videos

  • Nucleotide sequence analysis of parental and recombinant plasmids.
  • Main Results:

    • In vivo recombination occurred between pHS1 and ColE1, forming recombinant plasmids.
    • A unique 1-kilobase sequence from pHS1 was duplicated at the junctions of integrated pHS1 within ColE1.
    • This 1-kilobase sequence was identified as a novel insertion sequence, IS102, with terminal inverted repeats and similarities to Tn903.
    • Recombination was RecA-independent.

    Conclusions:

    • The 1-kilobase sequence, IS102, is a novel insertion sequence mediating plasmid recombination.
    • IS102 exhibits characteristics of mobile genetic elements, including duplication and terminal repeats.
    • The findings contribute to the understanding of plasmid evolution and genetic diversity in bacteria.