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

Cellular identity and lineage choice.

Amanda G Fisher1

  • 1Lymphocyte Development Group, Medical Research Council Clinical Sciences Centre, Faculty of Medicine, Imperial College of Science, Technology and Medicine, Hammersmith Campus, Du Cane Road, London W12 0NN, UK. amanda.fisher@csc.mrc.ac.uk

Nature Reviews. Immunology
|December 4, 2002
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

SOX2 phosphorylation during mitosis limits genomic damage.

Genes & development·2025
Same author

PBK/TOPK mediates Ikaros, Aiolos and CTCF displacement from mitotic chromosomes and alters chromatin accessibility at selected C2H2-zinc finger protein binding sites.

Nature communications·2025
Same author

Hbo1 and Msl complexes preserve differential compaction and H3K27me3 marking of active and inactive X chromosomes during mitosis.

Nature cell biology·2025
Same author

Editorial: 10 years of Frontiers in cell and developmental biology: past discoveries, current challenges and future perspectives.

Frontiers in cell and developmental biology·2025
Same author

Extensive folding variability between homologous chromosomes in mammalian cells.

Molecular systems biology·2025
Same author

Competition shapes the landscape of X-chromosome-linked genetic diversity.

Nature genetics·2024
Same journal

A guide to CAR T cell therapies: development, current status and future prospects.

Nature reviews. Immunology·2026
Same journal

Macrophages in embryonic development.

Nature reviews. Immunology·2026
Same journal

Glycolytic capacity instructs tumour vasculature and response to immunotherapy.

Nature reviews. Immunology·2026
Same journal

Vaginal NK cells limit epithelial barrier disruption during infection.

Nature reviews. Immunology·2026
Same journal

New insights into progenitor exhausted T cell populations.

Nature reviews. Immunology·2026
Same journal

T cell engagers in autoimmune diseases.

Nature reviews. Immunology·2026
See all related articles

Somatic cells remember their developmental history through epigenetic mechanisms, influencing how they respond to signals. This

Area of Science:

  • Cell Biology
  • Developmental Biology
  • Epigenetics

Background:

  • Multicellular organisms exhibit cell-specific responses to external stimuli.
  • Cellular responses are influenced by developmental history, not solely by genome.
  • Somatic cells possess a 'working memory' of their lineage, passed via epigenetic information.

Purpose of the Study:

  • To explore how chromatin biology and gene silencing offer insights into cell fate determination.
  • To understand the mechanisms maintaining cell identity during development.

Main Methods:

  • Review of recent advances in chromatin biology.
  • Analysis of gene silencing mechanisms.
  • Discussion of epigenetic information inheritance.

Related Experiment Videos

Main Results:

  • Epigenetic information, including chromatin modifications and gene silencing, plays a crucial role in cell fate.
  • Cellular 'working memory' is maintained through epigenetic inheritance during cell division.
  • Advances in chromatin biology provide new perspectives on cell identity maintenance.

Conclusions:

  • Cell fate choice and maintenance are intricately linked to epigenetic mechanisms.
  • Understanding chromatin dynamics and gene silencing is key to deciphering cell lineage.
  • Epigenetic memory ensures developmental consistency and cell specialization.