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

Are there any normal clones?

Ian Wilmut1

  • 1Department of Gene Function and Development, Roslin Institute, Roslin, Midlothian, UK.

Methods in Molecular Biology (Clifton, N.J.)
|September 22, 2006
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

Endothelial Progenitor Cells Do Not Originate From the Bone Marrow.

Circulation·2019
Same author

Cloning After Dolly.

Cellular reprogramming·2018
Same author

C9ORF72 repeat expansion causes vulnerability of motor neurons to Ca<sup>2+</sup>-permeable AMPA receptor-mediated excitotoxicity.

Nature communications·2018
Same author

Towards the isolation of embryonal stem cell lines from the sheep.

Roux's archives of developmental biology : the official organ of the EDBO·2017
Same author

Development of an inducible platform for intercellular protein delivery.

International journal of pharmaceutics·2017
Same author

Chondrocytes Derived From Mesenchymal Stromal Cells and Induced Pluripotent Cells of Patients With Familial Osteochondritis Dissecans Exhibit an Endoplasmic Reticulum Stress Response and Defective Matrix Assembly.

Stem cells translational medicine·2016
Same journal

Mapping the 3D Chromosome Organization of a Biosynthetic Gene Cluster by Capture Hi-C (CHi-C).

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Mapping the 3D Chromosome Organization of Streptomyces by Hi-C.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

CUT&Tag Epigenomic Profiling of Biosynthetic Gene Clusters in Arabidopsis thaliana.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Rhizobium rhizogenes-Mediated Hairy Root Transformation Protocol for Lotus japonicus and Other Legumes.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Characterization of Bioactive Saponins from Sea Cucumbers.

Methods in molecular biology (Clifton, N.J.)·2026
Same journal

Methods for Functional Validation of Terpenoid Metabolic Clusters in Nicotiana benthamiana and Aspergillus oryzae.

Methods in molecular biology (Clifton, N.J.)·2026
See all related articles

Clone development shows prevalent abnormalities and variation compared to parents, often exceeding expectations. This highlights inherent stochasticity in nuclear transfer, necessitating careful documentation of observational data.

Area of Science:

  • Reproductive biology
  • Developmental biology
  • Genetics

Background:

  • Assessing clone fidelity to parent is challenging due to cost and experimental scope.
  • Existing observational data lack standardization, hindering definitive analysis of clone abnormalities and variation.
  • Literature surveys are crucial for gathering evidence on clone infidelity.

Purpose of the Study:

  • To survey and document clone developmental abnormalities and variation.
  • To identify factors influencing clone infidelity, such as nuclear donor cell choice and stochastic nuclear transfer responses.
  • To emphasize the value of meticulous observational data collection in the absence of controlled hypothesis testing.

Main Methods:

  • Literature survey of existing observational evidence on clone fidelity.

Related Experiment Videos

  • Analysis of reported abnormalities and variations across developmental stages (cleavage, placental, fetal, neonatal, maturity).
  • Identification of potential sources of variation, including study protocols and nuclear donor cell selection.
  • Main Results:

    • Clone developmental abnormalities and variation are prevalent at most stages.
    • Observed variations occasionally greatly exceed expected levels.
    • Differences in study protocols and nuclear donor cell choice influence observed variation.

    Conclusions:

    • Nuclear transfer inherently involves stochastic responses leading to clone infidelity and variation.
    • Meticulous documentation of observational evidence is valuable for understanding clone health and fidelity.
    • Future studies should contribute to a comprehensive record of clone abnormalities and variations.