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Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
Role of Hematopoietic Growth Factors01:28

Role of Hematopoietic Growth Factors

Hematopoietic growth factors are molecules that regulate the differentiation rate of hematopoietic stem cells (HSCs). Erythropoietin (EPO), primarily produced by the kidneys, plays a crucial role in erythrocyte production. When oxygen levels in the blood are low, EPO is released into the bloodstream, reaching the bone marrow, where it stimulates HSCs to differentiate and mature into erythrocytes, which are vital for oxygen transport.
Thrombopoietin (TPO), mainly released by the liver,...
Regulation of Angiogenesis and Blood Supply01:24

Regulation of Angiogenesis and Blood Supply

Rapidly dividing tumors, embryos, and wounded tissues require more oxygen than usual, lowering the oxygen concentration in the blood. At low oxygen or hypoxic conditions, an oxygen-sensitive transcription factor called the hypoxia-inducible factor 1 or HIF1 is activated. HIF1 is a dimeric protein of alpha (ɑ) and beta (β) subunits.  Under optimal oxygen conditions, HIF1β is present in the nucleus while HIF1ɑ remains in the cytosol. HIF1ɑ is hydroxylated by prolyl hydroxylase and factor...
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...
mTOR Signaling and Cancer Progression03:03

mTOR Signaling and Cancer Progression

The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
The mTOR pathway or the...
Epigenetic Regulation01:37

Epigenetic Regulation

Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...

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Related Experiment Video

Updated: Jul 10, 2026

Efficient Purification and LC-MS/MS-based Assay Development for Ten-Eleven Translocation-2 5-Methylcytosine Dioxygenase
10:33

Efficient Purification and LC-MS/MS-based Assay Development for Ten-Eleven Translocation-2 5-Methylcytosine Dioxygenase

Published on: October 15, 2018

Regulation of TET function by PROSER1 in development and hematologic malignancies.

Xiang Li1, Kasper D Rasmussen1

  • 1Division of Molecular, Cellular, and Developmental Biology, University of Dundee, Dundee, UK.

Epigenomics
|July 9, 2026
PubMed
Summary
This summary is machine-generated.

The Ten eleven translocation (TET) protein complex, including OGT, PROSER1, and DBHS, regulates DNA methylation and epigenetic homeostasis. This TOPD complex is crucial for development and preventing hematologic disorders.

Keywords:
PROSER1TET1TET2TET3hematopoiesisneurodevelopment

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Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
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Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells

Published on: February 21, 2018

Related Experiment Videos

Last Updated: Jul 10, 2026

Efficient Purification and LC-MS/MS-based Assay Development for Ten-Eleven Translocation-2 5-Methylcytosine Dioxygenase
10:33

Efficient Purification and LC-MS/MS-based Assay Development for Ten-Eleven Translocation-2 5-Methylcytosine Dioxygenase

Published on: October 15, 2018

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
10:21

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells

Published on: February 21, 2018

Area of Science:

  • Epigenetics and Molecular Biology
  • DNA Methylation Dynamics
  • Protein-Protein Interactions

Background:

  • Ten eleven translocation (TET) proteins are key regulators of DNA methylation homeostasis, essential for development and implicated in hematopoietic malignancies.
  • Mutations in TET2 are common in hematologic disorders, underscoring the importance of TET protein function.
  • TET enzymes mediate DNA demethylation through oxidation of 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) and further derivatives.

Purpose of the Study:

  • To review the assembly and function of the TOPD (TET-OGT-PROSER1-DBHS) complex.
  • To elucidate the role of the TOPD complex in multicomponent regulation of TET proteins.
  • To discuss the implications of the TOPD complex in epigenetic homeostasis and disease.

Main Methods:

  • Literature review of studies on TET proteins, OGT, PROSER1, and DBHS proteins.
  • Analysis of protein-protein interactions and complex formation.
  • Integration of findings to propose the TOPD complex as a regulatory unit.

Main Results:

  • TET proteins, OGT, PROSER1, and DBHS proteins form a higher-order regulatory unit called the TOPD complex.
  • The TOPD complex integrates enzymatic and non-enzymatic functions of TET proteins.
  • This complex provides a framework for understanding spatial control of DNA demethylation.

Conclusions:

  • The TOPD complex offers a new perspective on the regulation of TET protein function and epigenetic homeostasis.
  • Understanding the TOPD complex is vital for comprehending developmental syndromes and hematopoiesis.
  • Further research into the TOPD complex could reveal therapeutic targets for hematologic disorders.