Compare and contrast broad sense heritability and narrow sense heritability, giving an example of each measurement and identifying how the measurement is used.
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
3. Extensions to Mendelian Inheritance
Overview of interacting Genes
Problem 7f
Textbook Question
Provide a definition and an example for each of the following terms:
Threshold trait

1
A threshold trait is a type of polygenic trait that is influenced by multiple genes and environmental factors, but it is expressed in a discrete (all-or-none) manner rather than a continuous range. For example, a person either has the trait or does not, depending on whether their genetic and environmental factors exceed a certain threshold.
Begin by understanding that threshold traits are often associated with complex diseases or conditions, such as Type 2 diabetes or cleft palate, where a combination of genetic predisposition and environmental triggers determines whether the condition manifests.
To explain this concept, consider a hypothetical example: Susceptibility to Type 2 diabetes. Multiple genes contribute to the risk, and environmental factors like diet and exercise also play a role. If the combined genetic and environmental risk factors exceed a certain threshold, the individual develops the disease.
Visualize the concept using a graph: On the x-axis, plot the cumulative genetic and environmental risk factors, and on the y-axis, indicate the presence or absence of the trait. The threshold is a specific point on the x-axis; individuals to the right of this point express the trait, while those to the left do not.
Finally, emphasize that threshold traits differ from continuous traits (e.g., height or weight) because they are expressed in a binary manner (present or absent), even though they are influenced by multiple factors.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Threshold Trait
A threshold trait is a type of genetic trait that is not continuously distributed but instead manifests only when a certain threshold of genetic or environmental factors is reached. For example, a person may have a genetic predisposition to a condition like diabetes, but the disease will only develop if they exceed a specific threshold of risk factors, such as obesity or lack of exercise.
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Polygenic Inheritance
Threshold traits often arise from polygenic inheritance, where multiple genes contribute to a single phenotype. Each gene may have a small effect, and the cumulative impact of these genes determines whether the threshold is crossed. This complexity makes threshold traits more challenging to predict compared to traits governed by a single gene.
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Environmental Influences
Environmental factors play a crucial role in the expression of threshold traits. These factors can include lifestyle choices, diet, and exposure to toxins, which can interact with genetic predispositions. Understanding how these influences affect the likelihood of crossing the threshold is essential for comprehending the development of such traits.
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