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Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
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Hedgehog Signaling Pathway

The Hedgehog gene (Hh) was first discovered due to its control of the growth of disorganized, hair-like bristles phenotype in Drosophila, much like hedgehog spines. Hh plays a crucial role in the development of organs and the maintenance of homeostasis in both invertebrates and vertebrates. However, while Drosophila has only one Hh protein, mammals have multiple functional Hedgehog proteins - Sonic (Shh), Desert (Dhh), and Indian Hedgehog (Ihh). All of these homologous proteins have adapted to...
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
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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...
Epigenetic Regulation01:46

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Target Cell Response to Hormones01:22

Target Cell Response to Hormones

Hormones intricately bind to receptors on the surface or within target cells, initiating a cascade of cellular responses.
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Related Experiment Video

Updated: Jul 7, 2026

Assessment of the Effects of Endocrine Disrupting Compounds on the Development of Vertebrate Neural Network Function Using Multi-electrode Arrays
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Endocrine disruptors affect developmental programming of HOX gene expression.

Hugh S Taylor1

  • 1Division of Reproductive Endocrinology and Infertility, Department of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, Connecticut 06520, USA. hugh.taylor@yale.edu

Fertility and Sterility
|March 20, 2008
PubMed
Summary

HOX gene expression guides Müllerian duct development. Environmental chemicals like diethylstilbestrol disrupt this process by altering HOX genes, causing reproductive tract defects.

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Area of Science:

  • Reproductive biology
  • Developmental biology
  • Endocrinology

Background:

  • Müllerian duct development establishes the female reproductive tract.
  • HOX genes are critical regulators of embryonic development and tissue patterning.
  • Exposure to endocrine-disrupting chemicals can interfere with normal development.

Purpose of the Study:

  • To investigate the role of HOX gene expression in Müllerian duct development.
  • To determine how environmental xenoestrogens, such as diethylstilbestrol, affect HOX gene expression and reproductive tract development.

Main Methods:

  • Analysis of HOX gene expression patterns during Müllerian duct development.
  • In vivo and in vitro studies exposing reproductive tissues to diethylstilbestrol and other xenoestrogens.
  • Assessment of structural and functional outcomes in the female reproductive tract following chemical exposure.

Main Results:

  • HOX gene expression profiles define the specific developmental fate of the Müllerian duct.
  • Diethylstilbestrol and other environmental xenoestrogens significantly alter HOX gene expression.
  • Altered HOX gene expression leads to structural malformations and functional impairments of the female reproductive tract.

Conclusions:

  • HOX gene expression is a key determinant of Müllerian duct identity.
  • Environmental xenoestrogens pose a risk to female reproductive tract development by disrupting critical HOX gene regulation.
  • Understanding these mechanisms is crucial for addressing reproductive health issues linked to environmental exposures.