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

Cloning embryos by nuclear transfer.

R S Prather1, N L First

  • 1Department of Meat and Animal Science, College of Agricultural and Life Sciences, University of Wisconsin, Madison 53706.

Journal of Reproduction and Fertility. Supplement
|January 1, 1990
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

Knockout of SIGLEC1 in pigs reduces porcine reproductive and respiratory syndrome-1 (PRRSV-1) virus infection in primary macrophage cultures, but not in pigs.

Virology journal·2026
Same author

Effect of FGF2, LIF, IGF1 supplementation on pregnancy success following embryo transfer of in vitro derived embryos.

Theriogenology·2025
Same author

Effects of RAD51-stimulatory compound 1 (RS-1) and its vehicle, DMSO, on pig embryo culture.

Reproductive toxicology (Elmsford, N.Y.)·2021
Same author

A novel swine sex-linked marker and its application across different mammalian species.

Transgenic research·2020
Same author

Emerging applications of sperm, embryo and somatic cell cryopreservation in maintenance, relocation and rederivation of swine genetics.

Theriogenology·2012
Same author

Regulation of oocyte mitochondrial DNA copy number by follicular fluid, EGF, and neuregulin 1 during in vitro maturation affects embryo development in pigs.

Theriogenology·2012
Same journal

Effect of transport on the intensity of stress reactions in mares and foals.

Journal of reproduction and fertility. Supplement·2010
Same journal

Gastrointestinal and endocrine function during 'foal heat diarrhoea' in healthy foals.

Journal of reproduction and fertility. Supplement·2010
Same journal

Response of newborn foals with thyroid musculoskeletal disease to adrenocorticotrophic hormone (ACTH).

Journal of reproduction and fertility. Supplement·2010
Same journal

Maternal influence on pre- and postnatal growth of foals born after embryo transfer.

Journal of reproduction and fertility. Supplement·2010
Same journal

Developmental changes in blood pressure and the renin-angiotensin system in pony fetuses during the second half of gestation.

Journal of reproduction and fertility. Supplement·2010
Same journal

The effects of oxytocin and progestagens on myometrial contractility in vitro during equine pregnancy.

Journal of reproduction and fertility. Supplement·2010
See all related articles

Nuclear transfer enables studying embryogenesis and creating identical individuals. Nuclear reprogramming in oocytes is key for development, but cell cycle asynchronies can limit success.

Area of Science:

  • Developmental biology
  • Cell biology
  • Reproductive biology

Background:

  • Nuclear transfer is a technique to study cell differentiation and produce cloned organisms.
  • Transferred nuclei undergo significant changes within the oocyte cytoplasm, including swelling and protein exchange.

Purpose of the Study:

  • To investigate the genomic modifications occurring after nuclear transfer.
  • To understand the limitations in development associated with differentiated donor nuclei.

Main Methods:

  • Analysis of nuclear changes (swelling, DNA synthesis, protein exchange) post-transfer.
  • Comparison of nuclear reprogramming efficiency in different species (amphibians, mammals).

Main Results:

  • Nuclear transfer induces swelling, DNA synthesis, and protein exchange, aiming for zygotic nucleus behavior.

Related Experiment Videos

  • Developmental limitations are linked to cell cycle asynchronies and incomplete genomic reprogramming.
  • Incomplete DNA synthesis and reprogramming precede the first cell division.
  • Conclusions:

    • Genomic modifications are crucial for successful nuclear reprogramming after transfer.
    • Cell cycle asynchronies and insufficient reprogramming limit developmental potential.
    • Understanding these nuclear modifications is vital for improving cloning efficiency and developmental studies.