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Gene-Environment Interactions01:20

Gene-Environment Interactions

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Gene expression is a dynamic process that is significantly influenced by environmental factors. This interaction underlies the complex nature of biological development and the phenotypic differences observed among individuals, even among those with identical genetic makeups. Factors such as radiation, temperature, behavior, nutrition, and stress play pivotal roles in determining how genes are expressed. The concept of the reaction range is central to understanding this interaction. It posits...
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Background and Environment Affect Phenotype02:27

Background and Environment Affect Phenotype

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Although the genetic makeup of an organism plays a major role in determining the phenotype, there are also several environmental factors, such as temperature, oxygen availability, presence of mutagens, that can alter an organism’s phenotype.
An example of how genetic background affects phenotype can be seen in horses. The Extension gene in horses is responsible for their coat color. A wild-type gene (EE) produces black pigment in the coat, while a mutant gene (ee) produces red pigment. A...
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Behavioral Genetics and Its Designs01:23

Behavioral Genetics and Its Designs

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Behavior genetics explores how genetic inheritance influences human behavior. It focuses on how genes, passed from parents to offspring, contribute to the development of behavioral traits and tendencies. This branch of genetics seeks to understand the complex interplay between inherited genetic factors and environmental influences in shaping our behaviors.
The primary methodologies used in behavior genetics include family studies, twin studies, and adoption studies, each providing unique...
857
Epistasis Analysis01:09

Epistasis Analysis

5.5K
Although Mendel chose seven unrelated traits in peas to study gene segregation, most traits involve multiple gene interactions that create a spectrum of phenotypes. When the interaction of various genes or alleles at different locations influences a phenotype, this is called epistasis. Epistasis often involves one gene masking or interfering with the expression of another (antagonistic epistasis). Epistasis often occurs when different genes are part of the same biochemical pathway. The...
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Teratogenicity01:07

Teratogenicity

3.8K
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...
3.8K
Genomic Imprinting and Inheritance02:30

Genomic Imprinting and Inheritance

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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.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
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Related Experiment Video

Updated: Dec 14, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

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Gene-environment interactions: aligning birth defects research with complex etiology.

Tyler G Beames1,2, Robert J Lipinski3,2

  • 1Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI 53706, USA.

Development (Cambridge, England)
|July 19, 2020
PubMed
Summary
This summary is machine-generated.

Gene-environment interactions significantly influence congenital abnormalities, impacting genetic disorder severity. Understanding these complex relationships is crucial for identifying and mitigating avoidable risks in vulnerable populations.

Keywords:
Birth defectGene-environment interactionHoloprosencephalyMicrophysiological modelOrganoidOrofacial cleftsSonic hedgehog

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Area of Science:

  • Developmental biology
  • Genetics
  • Environmental health

Background:

  • Genomics advances facilitate gene-disease relationship studies.
  • Nonsyndromic birth defects often display complex inheritance patterns.
  • Genotype-phenotype discordance highlights the role of extrinsic factors.

Purpose of the Study:

  • To illustrate the importance of gene-environment interactions in birth defect etiology.
  • To address challenges in resolving these interactions.
  • To propose strategies for improved understanding and intervention.

Main Methods:

  • Utilizing mouse models of sonic hedgehog signaling and craniofacial malformations.
  • Investigating gene-environment interactions in congenital abnormalities.
  • Proposing the use of genetically tractable and environmentally responsive in vitro systems.

Main Results:

  • Mouse models demonstrate the impact of gene-environment interactions on craniofacial development.
  • Challenges in resolving these interactions were identified.
  • Potential solutions involving in vitro systems were outlined.

Conclusions:

  • Gene-environment interactions are critical in birth defect etiology.
  • Overlooking these interactions limits risk identification and prevention.
  • Combining diverse approaches will advance birth defect research and protect vulnerable groups.