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Related Concept Videos

Inheritance of Chromatin Structures03:17

Inheritance of Chromatin Structures

Epigenetics is the study of inherited changes in a cell's phenotype without changing the DNA sequences. It provides a form of memory for the differential gene expression pattern to maintain cell lineage, position-effect variegation, dosage compensation, and maintenance of chromatin structures such as telomeres and centromeres. For example, the structure and location of the centromere on chromosomes are epigenetically inherited. Its functionality is not dictated or ensured by the underlying DNA...
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.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
Background and Environment Affect Phenotype02:27

Background and Environment Affect Phenotype

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...
Dosage Compensation02:50

Dosage Compensation

In animals, gender is determined by the number and type of sex chromosome. For example, human females have two X chromosomes, and males have one X and one Y chromosome, whereas C.elegans with one X chromosome is a male, and the one with two X chromosomes is a hermaphrodite.
In addition to sexual development, the X chromosome has genes involved in autosomal functions such as brain development and the immune system. Therefore, males and females with  distinct numbers of X chromosomes will have...
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

Epigenetic Regulation

Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.

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Stable Isotope In-Vivo Labeling for Mass-Spectrometry Identification of Paternal Metabolites Transferred from Sperm to Oocyte During Fertilization
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Sex-specificity in transgenerational epigenetic programming.

Gregory A Dunn1, Christopher P Morgan, Tracy L Bale

  • 1Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Hormones and Behavior
|May 21, 2010
PubMed
Summary
This summary is machine-generated.

Maternal prenatal experiences like stress and diet can epigenetically program offspring, influencing health across generations. This review highlights how embryo sex impacts these epigenetic changes and inherited traits.

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Area of Science:

  • Epigenetics and Developmental Biology
  • Reproductive Health and Disease

Background:

  • Prenatal environment critically influences offspring health via epigenetic programming.
  • Maternal stress and obesity link to multi-generational neurodevelopmental and metabolic diseases.
  • Epigenetic mechanisms involve maternal environment, placenta, and embryo interactions.

Purpose of the Study:

  • To review the role of embryo sex in epigenetic regulation.
  • To explore sex-specific differences in trait inheritance from prenatal exposures.
  • To discuss the impact of maternal stress and diet on sex-specific epigenetic programming.

Main Methods:

  • Review of existing literature on prenatal programming, epigenetics, and sex differences.
  • Analysis of models involving maternal stress and diet.
  • Examination of multi-generational effects on offspring health.

Main Results:

  • Prenatal programming affects offspring epigenome, influencing disease risk.
  • Maternal factors like stress and diet can lead to transgenerational health outcomes.
  • Embryo sex is an underappreciated factor in epigenetic regulation and trait inheritance.

Conclusions:

  • Sex differences are crucial in understanding the inheritance of epigenetically programmed traits.
  • Further research into sex-specific epigenetic mechanisms is needed to address developmental and metabolic diseases.
  • Integrating sex as a biological variable is essential for comprehensive prenatal programming research.