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Related Concept Videos

Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012 for this...
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The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...
Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for injury repair.
Combinatorial Gene Control02:33

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Combinatorial gene control is the synergistic action of several transcriptional factors to regulate the expression of a single gene. The absence of one or more of these factors may lead to a significant difference in the level of gene expression or repression.
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Zygotic Development And Stem Cell Formation01:10

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The development of all multicellular organisms starts with the fusion of haploid cells called sperm and egg to form a diploid zygote. A zygote is a totipotent cell that can develop into a complete organism. The zygote undergoes cell division or cleavage to form an 8-cell mass. Until this stage, the cells are spherical, loosely attached, and remain totipotent. Totipotent cells are capable of developing both the embryonic and the extraembryonic tissues. However, as they continue to divide, they...
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Related Experiment Video

Updated: Jul 6, 2026

Generation of Human Primordial Germ Cell-like Cells at the Surface of Embryoid Bodies from Primed-pluripotency Induced Pluripotent Stem Cells
12:06

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Requirement of Oct3/4 function for germ cell specification.

Daiji Okamura1, Yuko Tokitake, Hitoshi Niwa

  • 1Cell Resource Center for Biomedical Research, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-machi, Sendai 980-8575, Japan.

Developmental Biology
|April 9, 2008
PubMed
Summary
This summary is machine-generated.

The transcription factor Oct3/4 is essential for primordial germ cell (PGC) specification in mammalian embryos. Loss of Oct3/4 prevents PGC formation, but restoring its expression allows PGC development.

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Generation of Human Primordial Germ Cell-like Cells at the Surface of Embryoid Bodies from Primed-pluripotency Induced Pluripotent Stem Cells
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Oct4GiP Reporter Assay to Study Genes that Regulate Mouse Embryonic Stem Cell Maintenance and Self-renewal

Published on: May 30, 2012

Area of Science:

  • Developmental Biology
  • Genetics
  • Stem Cell Biology

Background:

  • Primordial germ cells (PGCs) are the precursors to gametes.
  • PGC specification in mammals occurs post-implantation from epiblast cells.
  • The transcription factor Oct3/4 is crucial for maintaining pluripotency.

Purpose of the Study:

  • To investigate the role of Oct3/4 in PGC specification.
  • To determine if Oct3/4 is essential for mammalian PGC development.

Main Methods:

  • Generation of chimeric embryos using Oct3/4-deficient ES cells with a suppressible Oct3/4 transgene.
  • Manipulation of Oct3/4 expression using doxycycline (Dox) and dexamethasone (Dex).
  • Analysis of ES cell contribution to PGC precursors and PGCs in chimeric embryos.

Main Results:

  • ES cells lacking Oct3/4 failed to form PGCs, even when contributing to PGC precursors.
  • Constitutive suppression of Oct3/4 transgene in chimeric embryos without Dox prevented PGC formation.
  • Restoring Oct3/4 expression via an additional transgene or Dex-dependent system rescued PGC specification.

Conclusions:

  • Oct3/4 is indispensable for the specification of primordial germ cells from epiblast-derived cells.
  • The study confirms the critical role of Oct3/4 in germline development.
  • Conditional rescue experiments validate Oct3/4's necessity for PGC formation.