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Related Concept Videos

Embryonic Stem Cells00:58

Embryonic Stem Cells

Embryonic stem (ES) cells are undifferentiated pluripotent cells, meaning they can produce any cell type in the body. This gives them tremendous potential in science and medicine since they can generate specific cell types for use in research or to replace body cells lost due to damage or disease.
Embryonic Stem Cells00:57

Embryonic Stem Cells

Embryonic stem (ES) cells were first discovered in mice in 1981 by Martin Evans. In 1998, James Thomson identified a method to isolate embryonic stem cells from humans. Human embryonic stem cells (hESCs) are obtained from 3-5 day old embryos that remain unused after an in vitro fertilization procedure.
ES cells are grown in a culture medium where they can divide indefinitely, creating ES cell lines. Under certain conditions, ES cells can differentiate, either spontaneously into a variety of...
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...
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.
Gastrulation01:56

Gastrulation

Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of intricate cellular movements, which in humans transforms a flat, “bilaminar disc” composed of two cell sheets into a three-tiered structure. In the resulting embryo, the endoderm serves as the bottom layer, and stacked directly above it is the intermediate mesoderm, and then the uppermost ectoderm. Respectively, these tissue strata will form...

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Related Experiment Video

Updated: May 27, 2026

Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation
09:07

Prediction and Validation of Gene Regulatory Elements Activated During Retinoic Acid Induced Embryonic Stem Cell Differentiation

Published on: June 21, 2016

Embryonic stem cell-based mapping of developmental transcriptional programs.

Esteban O Mazzoni1, Shaun Mahony, Michelina Iacovino

  • 1Departments of Pathology, Neurology and Neuroscience, Center for Motor Neuron Biology and Disease and Columbia Stem Cell Initiative, Columbia University Medical Center, New York, New York, USA.

Nature Methods
|November 15, 2011
PubMed
Summary

Researchers developed a new method to map transcription factor binding sites using stem cell differentiation and inducible protein expression. This technique overcomes challenges in antibody availability and cell numbers for ChIP-seq studies.

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Last Updated: May 27, 2026

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Area of Science:

  • Developmental biology
  • Genomics
  • Molecular biology

Background:

  • Chromatin immunoprecipitation and deep sequencing (ChIP-seq) is crucial for studying transcription factor binding.
  • Current ChIP-seq methods face limitations due to antibody availability and cell number requirements.

Purpose of the Study:

  • To develop a versatile method for genome-wide analysis of transcription-factor binding sites.
  • To overcome existing obstacles in ChIP-seq studies of developmentally regulated factors.

Main Methods:

  • Combining directed differentiation of embryonic stem cells with inducible expression of tagged proteins.
  • Utilizing the developed method for mapping DNA-binding sites.

Main Results:

  • Successfully mapped DNA-binding sites of transcription factors involved in motor neuron specification.
  • Demonstrated the utility of the combined approach.

Conclusions:

  • The described method provides a versatile approach for genome-wide transcription factor analysis.
  • This technique enhances ChIP-seq applicability, particularly for developmentally regulated factors and limited cell samples.