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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...
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.
Introduction to Nuclear Reprogramming01:14

Introduction to Nuclear Reprogramming

Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Combinatorial Gene Control02:33

Combinatorial Gene Control

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.
The expression of more than 30,000 genes is controlled by approximately 2000-3000 transcription factors. This is possible because a single transcription factor can recognize more than one regulatory sequence. The specificity in gene...

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Related Experiment Video

Updated: Jun 4, 2026

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans
07:53

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

Published on: January 1, 2018

A germ cell-specific gene, Prmt5, works in somatic cell reprogramming.

Go Nagamatsu1, Takeo Kosaka, Miyuri Kawasumi

  • 1Department of Cell Differentiation, The Sakaguchi Laboratory, School of Medicine, Keio University, Tokyo 160-8582, Japan. gonag@sc.itc.keio.ac.jp

The Journal of Biological Chemistry
|January 29, 2011
PubMed
Summary

Primordial germ cells (PGCs) hold keys to reprogramming. Factors like Prmt5, crucial for PGC development, can efficiently convert somatic cells into pluripotent stem cells, similar to embryonic stem cells.

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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
12:06

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

Published on: January 11, 2019

Related Experiment Videos

Last Updated: Jun 4, 2026

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans
07:53

Application of RNAi and Heat-shock-induced Transcription Factor Expression to Reprogram Germ Cells to Neurons in C. elegans

Published on: January 1, 2018

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

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

Published on: January 11, 2019

Area of Science:

  • Stem cell biology
  • Developmental biology
  • Epigenetics

Background:

  • Germ cells exhibit unique totipotency and can generate pluripotent stem cells.
  • Genes like Oct3/4, Sox2, and Lin28, active in primordial germ cells (PGCs), are implicated in somatic cell reprogramming.
  • PGCs may offer insights into factors for efficient somatic cell reprogramming.

Purpose of the Study:

  • To investigate the potential of PGC development factors in reprogramming somatic cells.
  • To identify specific factors that can efficiently convert somatic cells into pluripotent stem cells.

Main Methods:

  • Expression analysis of PGC development factors (Blimp-1, Prdm14, Prmt5).
  • Introduction of Prmt5, Klf4, and Oct3/4 into mouse embryonic fibroblasts (MEFs).
  • Assessment of reprogrammed cell pluripotency through gene expression, teratoma formation, and germline transmission in chimeric mice.

Main Results:

  • Blimp-1, Prdm14, and Prmt5 demonstrate potential for somatic cell reprogramming.
  • Prmt5, in combination with Klf4 and Oct3/4, achieved remarkable reprogramming of MEFs.
  • Reprogrammed cells displayed characteristics indistinguishable from embryonic stem cells, including pluripotent gene expression, teratoma formation, and germline transmission.

Conclusions:

  • Factors essential for germ cell development, such as Prmt5, are active in somatic cell reprogramming.
  • PGC development factors represent a promising avenue for efficient somatic cell reprogramming strategies.
  • This study highlights the conserved roles of germ cell factors in developmental plasticity and reprogramming.