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

Sialylation is essential for early development in mice.

Martina Schwarzkopf1, Klaus-Peter Knobeloch, Elvira Rohde

  • 1Institut für Molekularbiologie und Biochemie, Fachbereich Humanmedizin, Freie Universität Berlin, Arnimallee 22, D-14195 Berlin-Dahlem, Germany.

Proceedings of the National Academy of Sciences of the United States of America
|April 4, 2002
PubMed
Summary

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

Csf1r-mediated depletion of myeloid cells prevents dopaminergic neuron loss during chronic colitis.

Journal of neuroinflammation·2026
Same author

USP24 is a cross-reactive DUB targeting MOV10 to regulate IFN-I production.

Nature communications·2026
Same author

Inflammatory stimulus enhances synaptic material uptake by adult APP microglia in a microfluidic neuron-microglia co-culture model.

Journal of neuroinflammation·2026
Same author

Proximity labeling reveals non-catalytic interactions between DPP9 and ubiquitin signaling complexes.

Cellular and molecular life sciences : CMLS·2026
Same author

Gne-Depletion in C2C12 Myoblasts Leads to Alterations in Glycosylation and Myopathogene Expression.

Cells·2026
Same author

High-Throughput Synthesis and Screening of a Cyanimide Library Identifies Selective Inhibitors of ISG15-Specific Protease mUSP18.

Angewandte Chemie (International ed. in English)·2025

Inactivation of the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (UDP-GlcNAc 2-epimerase) enzyme causes early embryonic lethality in mice. This highlights the critical role of sialylation in embryonic development.

Area of Science:

  • Biochemistry
  • Developmental Biology
  • Glycobiology

Background:

  • Sialic acids are terminal carbohydrates on eukaryotic cell glycoconjugates, essential for cellular functions like adhesion and signal recognition.
  • Sialylation regulates glycoprotein stability and is vital for various biological processes.
  • The bifunctional UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase (UDP-GlcNAc 2-epimerase) is the key enzyme in sialic acid biosynthesis.

Purpose of the Study:

  • To investigate the essential role of UDP-GlcNAc 2-epimerase in sialic acid biosynthesis and its impact on embryonic development.
  • To demonstrate the fundamental importance of sialylation during early development.

Main Methods:

  • Gene targeting was employed to inactivate the UDP-GlcNAc 2-epimerase gene in mice.

Related Experiment Videos

  • Embryonic stem cells were utilized to study the polysialylation of the neural cell adhesion molecule.
  • Main Results:

    • Inactivation of UDP-GlcNAc 2-epimerase resulted in early embryonic lethality in mice.
    • The study demonstrated the necessity of UDP-GlcNAc 2-epimerase for proper sialylation processes, exemplified by neural cell adhesion molecule polysialylation.

    Conclusions:

    • The bifunctional UDP-GlcNAc 2-epimerase is indispensable for embryonic development due to its role in sialic acid biosynthesis.
    • Sialylation, regulated by UDP-GlcNAc 2-epimerase, is fundamentally required for successful embryonic development.