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

Jumping translocations.

Roland Berger1, Olivier A Bernard

  • 1EMI 0210 INSERM, Hôpital Necker-Enfants Malades, Paris, France. berger@necker.fr

Genes, Chromosomes & Cancer
|April 21, 2007
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

<i>Tet2</i> deficiency promotes IgG1+ B-cell expansion and differentiation blockade through deregulation of the <i>Nfkbia</i>-c-Rel axis.

HemaSphere·2026
Same author

A multiomic analysis of Waldenström macroglobulinemia defines distinct disease subtypes.

Blood·2025
Same author

Progressive chromatin rewiring by ETO2::GLIS2 revealed in a genome-edited human iPSC model of pediatric leukemia initiation.

Blood·2024
Same author

The ETO2 transcriptional cofactor maintains acute leukemia by driving a MYB/EP300-dependent stemness program.

HemaSphere·2024
Same author

Prognostic impact of genetic abnormalities in 536 first-line chronic lymphocytic leukaemia patients without 17p deletion treated with chemoimmunotherapy in two prospective trials: Focus on IGHV-mutated subgroups (a FILO study).

British journal of haematology·2024
Same author

Precision Medicine Approach Based on Molecular Alterations for Patients with Relapsed or Refractory Multiple Myeloma: Results from the MM-EP1 Study.

Cancers·2023

Jumping translocations (JT) are rare chromosome rearrangements. Their breakpoints cluster in specific chromosome regions, differing between inherited and acquired forms, suggesting distinct formation mechanisms.

Area of Science:

  • Cytogenetics
  • Genetics
  • Molecular Biology

Background:

  • Jumping translocations (JT) are uncommon chromosome rearrangements involving one donor and multiple recipient chromosomes.
  • These rearrangements occur in various pathologic conditions, but their formation mechanism remains unclear.
  • Previous studies indicate breakpoints in JTs are nonrandomly localized in pericentromeric and telomeric chromosome regions.

Purpose of the Study:

  • To review the literature on jumping translocations.
  • To analyze the localization of chromosomal breakpoints in JTs.
  • To compare breakpoint localization and DNA repeat presence in constitutional versus acquired JTs to infer mechanistic differences.

Main Methods:

  • Literature review of human samples with jumping translocations.

Related Experiment Videos

  • Analysis of breakpoint localization within chromosome structures.
  • Comparison of breakpoint distribution and interstitial DNA repeat presence.
  • Main Results:

    • Breakpoint localizations for JTs were nonrandomly identified in pericentromeric and telomeric regions.
    • Differences in breakpoint localization and interstitial DNA repeat presence were observed between constitutional and acquired JTs.
    • These findings suggest distinct mechanisms underlying the genesis of constitutional and acquired JTs.

    Conclusions:

    • Jumping translocations exhibit nonrandom breakpoint clustering in specific chromosomal regions.
    • Distinct patterns in breakpoint localization and DNA repeat content differentiate constitutional and acquired JTs.
    • The observed differences suggest divergent molecular mechanisms drive the formation of constitutional and acquired jumping translocations.