Created by: CK-12/Adapted by Christine Miller
Figure 5.14.1 Collage of Diverse Faces.
This collage shows some of the variation in human skin colour, which can range from very light to very dark, with every possible gradation in between. As you might expect, the skin color trait has a more complex genetic basis than just one gene with two alleles, which is the type of simple trait that Mendel studied in pea plants. Like skin color, many other human traits have more complicated modes of inheritance than Mendelian traits. Such modes of inheritance are called , and they include inheritance of multiple allele traits, traits with codominance or incomplete dominance, and polygenic traits, among others. All of these modes are described below.
Multiple Allele Traits
The majority of human genes are thought to have more than two normal versions, or alleles. Traits controlled by a single gene with more than two alleles are called . An example is ABO blood type. Your blood type refers to which of certain proteins called antigens are found on your red blood cells. There are three common alleles for this trait, which are represented by the letters A, B, and O.
As shown in the table there are six possible ABO genotypes, because the three alleles, taken two at a time, result in six possible combinations. The A and B alleles are dominant to the O allele. As a result, both AA and AO genotypes have the same phenotype, with the A antigen in their blood (type A blood). Similarly, both BB and BO genotypes have the same phenotype, with the B antigen in their blood (type B blood). No antigen is associated with the O allele, so people with the OO genotype have no antigens for ABO blood type in their blood (type O blood).
Codominance
Look at the genotype AB in the ABO blood group table. Alleles A and B for ABO blood type are neither nor to one another. Instead, they are codominant. occurs when two alleles for a gene are expressed equally in the phenotype of . In the case of ABO blood type, AB heterozygotes have a unique phenotype, with both A and B antigens in their blood (type AB blood).
Incomplete Dominance
Another relationship that may occur between alleles for the same gene is . This occurs when the dominant allele is not completely dominant. In this case, an intermediate phenotype results in heterozygotes who inherit both alleles. Generally, this happens when the two alleles for a given gene both produce proteins, but one protein is not functional. As a result, the heterozygote individual produces only half the amount of normal protein as is produced by an individual who is homozygous for the normal allele.
An example of incomplete dominance in humans is Tay Sachs disease. The normal allele for the gene in this case produces an that is responsible for breaking down . A defective allele for the gene results in the production of a nonfunctional enzyme. Heterozygotes who have one normal and one defective allele produce half as much functional enzyme as the normal homozygote, and this is enough for normal development. Homozygotes who have only defective allele, however, produce only nonfunctional enzyme. This leads to the accumulation of lipids in the brain starting in utero, which causes significant brain damage. Most individuals with Tay Sachs disease die at a young age, typically by the age of five years.
Another good example of incomplete dominance in humans is hair type. There are genes for straight and curly hair, and if an individual is heterozygous, they will typically have the phenotype of wavy hair.
Polygenic Traits
Many human traits are controlled by more than one gene. These traits are called . The alleles of each gene have a minor additive effect on the phenotype. There are many possible combinations of alleles, especially if each gene has multiple alleles. Therefore, a whole continuum of phenotypes is possible.
An example of a human polygenic trait is adult height. Several genes, each with more than one allele, contribute to this trait, so there are many possible adult heights. One adult’s height might be 1.655 m (5.430 feet), and another adult’s height might be 1.656 m (5.433 feet). Adult height ranges from less than 5 feet to more than 6 feet, with males, on average, being somewhat taller than females. The majority of people fall near the middle of the range of heights for their sex, as shown in Figure 5.14.4.
Environmental Effects on Phenotype
Many traits are affected by the environment, as well as by genes. This may be especially true for polygenic traits. Adult height, for example, might be negatively impacted by poor diet or childhood illness. Skin color is another polygenic trait. There is a wide range of skin colors in people worldwide. In addition to differences in genes, differences in exposure to ultraviolet (UV) light cause some variation. As shown in Figure 5.14.5, exposure to UV light darkens the skin.
Pleiotropy
Some genes affect more than one phenotypic trait. This is called . There are numerous examples of pleiotropy in humans. They generally involve important proteins that are needed for the normal development or functioning of more than one organ system. An example of pleiotropy in humans occurs with the gene that codes for the main protein in collagen, a substance that helps form bones. This protein is also important in the ears and eyes. Mutations in the gene result in problems not only in bones, but also in these sensory organs, which is how the gene’s pleiotropic effects were discovered.
Another example of pleiotropy occurs with sickle cell anemia. This recessive genetic disorder occurs when there is a mutation in the gene that normally encodes the red blood cell called hemoglobin. People with the disorder have two alleles for sickle cell hemoglobin, so named for the sickle shape (pictured in Figure 5.14.6) that their red blood cells take on under certain conditions (like physical exertion). The sickle-shaped red blood cells clog small blood vessels, causing multiple phenotypic effects, including stunting of physical growth, certain bone deformities, kidney failure, and strokes.
Epistasis
Some genes affect the expression of other genes. This is called . Epistasis is similar to dominance, except that it occurs between different genes, rather than between different alleles for the same gene.
Albinism is an example of epistasis. A person with albinism has virtually no pigment in the skin. The condition occurs due to an entirely different gene than the genes that encode skin color. Albinism occurs because a protein called tyrosinase, which is needed for the production of normal skin pigment, is not produced, due to a gene . If an individual has the albinism mutation, he or she will not have any skin pigment, regardless of the skin color genes that were inherited.
Feature: My Human Body
Do you know your ABO blood type? In an emergency, knowing this valuable piece of information could possibly save your life. If you ever need a blood transfusion, it is vital that you receive blood that matches your own blood type. Why? If the blood transfused into your body contains an antigen that your own blood does not contain, antibodies in your blood plasma (the liquid part of your blood) will recognize the antigen as foreign to your body and cause a reaction called agglutination. In this reaction, the transfused red blood cells will clump together. The agglutination reaction is serious and potentially fatal.
Knowing the antigens and antibodies present in each of the ABO blood types will help you understand which type(s) of blood you can safely receive if you ever need a transfusion. This information is shown in Figure 5.14.7 for all of the ABO blood types. If you have blood type A, this means that your red blood cells have the A antigen and that your blood plasma contains anti-B antibodies. If you were to receive a transfusion of type B or type AB blood, both of which have the B antigen, your anti-B antibodies would attack the transfused red blood cells, causing agglutination.
You may have heard that people with blood type O are called “universal donors,” and that people with blood type AB are called universal recipients. People with type O blood have neither A nor B antigens in their blood, so if their blood is transfused into someone with a different ABO blood type, it causes no immune reaction, meaning they can donate blood to anyone. On the other hand, people with type AB blood have no anti-A or anti-B antibodies in their blood, so they can receive a transfusion of blood from anyone. Which blood type(s) can safely receive a transfusion of type AB blood, and which blood type(s) can be safely received by those with type O blood?
5.14 Summary
- refers to the inheritance of traits that have a more complex genetic basis than one with two and complete .
- Multiple allele traits are controlled by a single gene with more than two alleles. An example of a human multiple allele trait is ABO blood type, for which there are three common alleles: A, B, and O.
- occurs when two alleles for a gene are expressed equally in the of heterozygotes. A human example of codominance also occurs in the ABO blood type, in which the A and B alleles are codominant.
- is the case in which the dominant allele for a gene is not completely dominant to a recessive allele for the gene, so an intermediate phenotype occurs in who inherit both alleles. A human example of incomplete dominance is Tay Sachs disease, in which heterozygotes produce half as much functional enzyme as normal homozygotes.
- are controlled by more than one gene, each of which has a minor additive effect on the phenotype. This results in a whole continuum of phenotypes. Examples of human polygenic traits include skin color and adult height.
- Many traits are affected by the environment, as well as by genes. This may be especially true for polygenic traits. Skin color, for example, may be affected by exposure to UV light, and adult stature may be affected by diet or childhood disease.
- refers to the situation in which a gene affects more than one phenotypic trait. A human example of pleiotropy occurs with sickle cell anemia. People who inherit two alleles for this disorder have abnormal red blood cells and may exhibit multiple other phenotypic effects, such as stunting of physical growth, kidney failure, and strokes.
- is the situation in which one gene affects the expression of other genes. An example of epistasis is albinism, in which the albinism mutation negates the expression of skin color genes.
5.14 Review Questions
- What is non-Mendelian inheritance?
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- Explain why the human ABO blood group is an example of a multiple allele trait with codominance.
- What is incomplete dominance? Give an example of this type of non-Mendelian inheritance in humans.
- Explain the genetic basis of human skin color.
- How can the human trait of adult height be influenced by the environment?
- Define pleiotropy, and give a human example.
- Compare and contrast epistasis and dominance.
- What is the difference between pleiotropy and epistasis?
5.14 Explore More
Incomplete Dominance, Codominance, Polygenic Traits, and Epistasis!,
Amoeba Sisters, 2015.
Non-Mendelian Genetics, Teacher’s Pet, 2015.
Attributes
Figure 5.14.1
- Woman’s Face from Iran by Omid Armin on Unsplash is used under the Unsplash License (https://unsplash.com/license).
- Woman Wearing Black Coat by Anastasiya Pavlova on Unsplash is used under the Unsplash License (https://unsplash.com/license).
- Dark haired man, Queretaro, México by Leonel Hernandez Arteaga on Unsplash is used under the Unsplash License (https://unsplash.com/license). <not found on Unsplash>
- Man in White V-Neck T-Shirt (self) by Joseph Gonzalez on Unsplash is used under the Unsplash License (https://unsplash.com/license).
- Natural Redhead in Brazil by Gabriel Silvério on Unsplash is used under the Unsplash License (https://unsplash.com/license).
- Dark-Skinned Woman with Large White Rose by Oladimeji Oduns on Unsplash is used under the Unsplash License (https://unsplash.com/license).
Figure 5.14.2
ABO Blood Types Per Genotype by Christine Miller is released into the public domain (https://en.wikipedia.org/wiki/Public_domain).
Figure 5.14.3
Three Phenotypes of Hair Based on Inheritance/ Incomplete Dominance Hair by Christine Miller is released into the public domain (https://en.wikipedia.org/wiki/Public_domain).
Figure 5.14.4
Average height /Human Adult Height by CK-12 Foundation is used under a CC BY 3.0 (https://creativecommons.org/licenses/by-nc/3.0/) license.
©CK-12 Foundation Licensed under 
• Terms of Use • Attribution
Figure 5.14.5
Tan lines by katiebordner on Flickr is used under a CC BY 2.0 (https://creativecommons.org/licenses/by/2.0/) license.
Figure 5.14.6
Sickle cell anemia by OpenStax College on Wikimedia Commons is used under a CC BY 3.0 (https://creativecommons.org/licenses/by/3.0) ©
Figure 5.14.7
ABO_blood_type.svg by InvictaHOG on Wikimedia Commons is in the public domain (https://en.wikipedia.org/wiki/Public_domain).
References
Amoeba Sisters. (2015, May 25). Incomplete dominance, codominance, polygenic traits, and epistasis! YouTube. https://www.youtube.com/watch?v=YJHGfbW55l0
Betts, J. G., Young, K.A., Wise, J.A., Johnson, E., Poe, B., Kruse, D.H., Korol, O., Johnson, J.E., Womble, M., DeSaix, P. (2013, April 25). Figure 18.9 Sickle cells [digital image]. In Anatomy and Physiology. OpenStax. https://openstax.org/books/anatomy-and-physiology/pages/18-3-erythrocytes
Brainard, J/ CK-12 Foundation. (2016). Figure 2 Human adult height [digital image]. In CK-12 College Human Biology (Section 5.13) [online Flexbook]. CK12.org. https://www.ck12.org/book/ck-12-college-human-biology/section/5.13/
Mayo Clinic Staff. (n.d.). Tay-Sachs disease [online article]. MayoClinic.org. https://www.mayoclinic.org/diseases-conditions/tay-sachs-disease/symptoms-causes/syc-20378190
Mayo Clinic Staff. (n.d.). Sickle cell anemia [online article]. MayoClinic.org. https://www.mayoclinic.org/diseases-conditions/sickle-cell-anemia/symptoms-causes/syc-20355876
Teacher’s Pet. (2015, January 25). Non-mendelian genetics. YouTube. https://www.youtube.com/watch?v=-4vsio8TZrU
Any pattern of inheritance in which traits do not segregate in accordance with Mendel's laws. This includes inheritance of multiple allele traits, codominance, incomplete dominance and polygenic traits.
Traits controlled by a single gene with more than two alleles.
Refers to the relationship between two versions of a gene. Individuals receive two versions of each gene, known as alleles, from each parent. If the alleles of a gene are different, one allele will be expressed; it is the dominant gene. The effect of the other allele, called recessive, is masked.
A gene that can be masked by a dominant gene. In order to have a trait that is expressed by a recessive gene, such as blue eyes, you must get the gene for blue eyes from both of your parents.
Means that neither allele can mask the expression of the other allele.
An individual who has two different forms of a particular gene, one inherited from each parent.
A heredity pattern in which phenotype of the heterozygous genotype is distinct from and often intermediate to the phenotypes of the homozygous genotypes.
Biological molecules that lower amount the energy required for a reaction to occur.
A substance that is insoluble in water. Examples include fats, oils and cholesterol. Lipids are made from monomers such as glycerol and fatty acids.
One whose phenotype is influenced by more than one gene. Traits that display a continuous distribution, such as height or skin color, are polygenic.
Describes the genetic effect of a single gene on multiple phenotypic traits. The underlying mechanism is genes that code for a product that is either used by various cells or has a cascade-like signaling function that affects various targets.
A class of biological molecule consisting of linked monomers of amino acids and which are the most versatile macromolecules in living systems and serve crucial functions in essentially all biological processes.
A phenomenon in genetics in which the effect of a gene mutation is dependent on the presence or absence of mutations in one or more other genes, respectively termed modifier genes. In other words, the effect of the mutation is dependent on the genetic background in which it appears.
An alteration in the nucleotide sequence of the genome of an organism.
A sequence of nucleotides in DNA or RNA that codes for a molecule that has a function.
A variant form of a given gene, meaning it is one of two or more versions of a known mutation at the same place on a chromosome. It can also refer to different sequence variations for a several-hundred base-pair or more region of the genome that codes for a protein.
The phenomenon of one variant of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome.
The set of observable characteristics of an individual resulting from the interaction of its genotype with the environment.
