- Alleles and genes
- Fertilization terminology: gametes, zygotes, haploid, diploid
- Mendelian genetics
- Aneuploidy & chromosomal rearrangements
- Variation in a species
- Chromosomal inheritance
- Pedigree for determining probability of exhibiting sex linked recessive trait
- Pedigrees review
- Extranuclear inheritance 1
- Non-Mendelian genetics
- Gene environment interaction
- Phenotype plasticity
- Polygenic inheritance and environmental effects
- Environmental effects on phenotype
Traits that are controlled by multiple genes and/or influenced by the environment. Penetrance and expressivity.
How is height inherited?
If what you're really interested in is human genetics, learning about Mendelian genetics can sometimes be frustrating. You'll often hear a teacher use a human trait as an example in a genetics problem, but then say, "that's an oversimplification" or "it's much more complicated than that." So, what's actually going on with those interesting human traits, such as eye color, hair and skin color, height, and disease risk?
As an example, let's consider human height. Unlike a simple Mendelian characteristic, human height displays:
- Continuous variation. Unlike Mendel's pea plants, humans don’t come in two clear-cut “tall” and “short” varieties. In fact, they don't even come in four heights, or eight, or sixteen. Instead, it’s possible to get humans of many different heights, and height can vary in increments of inches or fractions of inches.
- A complex inheritance pattern. You may have noticed that tall parents can have a short child, short parents can have a tall child, and two parents of different heights may or may not have a child in the middle. Also, siblings with the same two parents may have a range of heights, ones that don't fall into distinct categories.
Simple models involving one or two genes can't accurately predict all of these inheritance patterns. How, then, is height inherited?
Height and other similar features are controlled not just by one gene, but rather, by multiple (often many) genes that each make a small contribution to the overall outcome. This inheritance pattern is sometimes called polygenic inheritance (poly- = many). For instance, a recent study found over 400 genes linked to variation in height.
When there are large numbers of genes involved, it becomes hard to distinguish the effect of each individual gene, and even harder to see that gene variants (alleles) are inherited according to Mendelian rules. In an additional complication, height doesn’t just depend on genetics: it also depends on environmental factors, such as a child’s overall health and the type of nutrition he or she gets while growing up.
In this article, we’ll examine how complex traits such as height are inherited. We'll also see how factors like genetic background and environment can affect the phenotype (observable features) produced by a particular genotype (set of gene variants, or alleles).
Human features like height, eye color, and hair color come in lots of slightly different forms because they are controlled by many genes, each of which contributes some amount to the overall phenotype. For example, there are two major eye color genes, but at least 14 other genes that play roles in determining a person’s exact eye color.
Looking at a real example of a human polygenic trait would get complicated, largely because we’d have to keep track of tens, or even hundreds, of different allele pairs (like the 400 involved in height!). However, we can use an example involving wheat kernels to see how several genes whose alleles "add up" to influence the same trait can produce a spectrum of phenotypes.
In this example, there are three genes that make reddish pigment in wheat kernels, which we’ll call A, B, and C. Each comes in two alleles, one of which makes pigment (the capital-letter allele) and one of which does not (the lowercase allele). These alleles have additive effects: the aa genotype would contribute no pigment, the Aa genotype would contribute some amount of pigment, and the AA genotype would contribute more pigment (twice as much as Aa). The same would hold true for the B and C genes.
Now, let’s imagine that two plants heterozygous for all three genes (AaBbCc) were crossed to one another. Each of the parent plants would have three alleles that made pigment, leading to pinkish kernels. Their offspring, however, would fall into seven color groups, ranging from no pigment whatsoever (aabbcc) and white kernels to lots of pigment (AABBCC) and dark red kernels. This is in fact what researchers have seen when crossing certain varieties of wheat.
This example shows how we can get a spectrum of slightly different phenotypes (something close to continuous variation) with just three genes. It’s not hard to imagine that, as we increased the number of genes involved, we’d be able to get even finer variations in color, or in another trait such as height.
Human phenotypes—and phenotypes of other organisms—also vary because they are affected by the environment. For instance, a person may have a genetic tendency to be underweight or obese, but his or her actual weight will depend on diet and exercise (with these factors often playing a greater role than genes). In another example, your hair color may depend on your genes—until you dye your hair purple!
One striking example of how environment can affect phenotype comes from the hereditary disorder phenylketonuria (PKU). People who are homozygous for disease alleles of the PKU gene lack activity of an enzyme that breaks down the amino acid phenylalanine. Because people with this disorder cannot get rid of excess phenylalanine, it rapidly builds up to toxic levels in their bodies.
If PKU is not treated, the extra phenylalanine can keep the brain from developing normally, leading to intellectual disability, seizures, and mood disorders. However, because PKU is caused by the buildup of too much phenylalanine, it can also be treated in a very simple way: by giving affected babies and children a diet low in phenylalanine.
If people with phenylketonuria follow this diet strictly from a very young age, they can have few, or even no, symptoms of the disorder. In many countries, all newborns are screened for PKU and similar genetic diseases shortly after birth through a simple blood test, as shown in the image above.
Variable expressivity, incomplete penetrance
Even for characteristics that are controlled by a single gene, it’s possible for individuals with the same genotype to have different phenotypes. For example, in the case of a genetic disorder, people with the same disease genotype may have stronger or weaker forms of the disorder, and some may never develop the disorder at all.
In variable expressivity, a phenotype may be stronger or weaker in different people with the same genotype. For instance, in a group of people with a disease-causing genotype, some might develop a severe form of the disorder, while others might have a milder form. The idea of expressivity is illustrated in the diagram below, with the shade of green representing the strength of the phenotype.
In incomplete penetrance, individuals with a certain genotype may or may not develop a phenotype associated with the genotype. For example, among people with the same disease-causing genotype for a hereditary disorder, some might never actually develop the disorder. The idea of penetrance is illustrated in the diagram below, with green or white color representing the presence or absence of a phenotype.
What causes variable expressivity and incomplete penetrance? Other genes and environmental effects are often part of the explanation. For example, disease-causing alleles of one gene may be suppressed by alleles of another gene elsewhere in the genome, or a person's overall health may influence the strength of a disease phenotype.
Want to join the conversation?
- how environment causes pku?(8 votes)
- The environment doesn't actually cause the PKU -- that is genetic. But the environment can cause it to express in the phenotype -- create symptoms -- based on the environment. The PKU gene simply causes a person to be unable to properly process phenylalanine (they lack an adequate amount of the necessary enzymes). If that person eats foods that are high in it, they can begin to express symptoms of that genetic mutation. If they limit or eliminate those foods, they often will have no symptoms.(40 votes)
- What's the difference between polygenic and epistasis?
It sounds like in both of them, multiple genes affect one trait.(7 votes)
- While a polygenic phenotype can occur without epistasis, if you have epistasis you must be dealing with a polygenic phenotype.
Polygenic just means that there are multiple genes involved in a phenotype.
Epistasis refers to situations where one allele masks the phenotypic effect of one or more alleles of another gene.(17 votes)
- I'm trying to calculate the probability of getting 6 second to darkest wheat cores using combinatorics. The way I think about it is:
the probability of getting AABBCc + AABbCC + AaBbCC,
or 1/4*1/4*1/2 + 1/4*1/2*1/4 + 1/2*1/4*1/4 = 6/64, but what if we are dealing with much more than 3 alleles from each parent? The result are seemingly fall under "pascal's triangle" distribution but the intuitive sense of why it's the case isn't that straightforward..(8 votes)
- how are we able to walk on the earth(4 votes)
- Can a disaster, natural or man-made, affect human traits?(3 votes)
- Quite interesting question!
I can think of radiation which causes mutations.
Definitely causes of mutations can affect human traits and phenotype, but not in the form that it will favor survival. Nonetheless, future generations may be less adaptable and degenerated (recall Chernobyl nuclear plant disaster or Minamata disease in Japan (caused by excessive mercury due to chemical industry).
My answer is definitely yes. Negative impact.(7 votes)
- Does anyone know anything about syndactyly and its genetic inheritance?(4 votes)
- Does this mean that some genetic diseases are affected by environment? Like, can the environment improve or worsen the symptoms?(4 votes)
- So I am very short for my age , yet my mom and dad are both tall but my mom is a little shorter than my dad . Why is that? Do i have a disease or something that affects my growth ?(3 votes)
- A short stature can be caused by a variety of causes. It could be genetic, a hormone known as growth hormone could be low in the body, or, in more serious cases, an underlying disease or condition may have contributed to your stature (I.E: tumors, malnutrition, mitochondrial disease). If you are otherwise healthy, it is most likely either genetic or hormonal.
Does this help?(2 votes)
- In the example with wheat kernels with Aa having some pigment and AA having a lot, does it have to do with incomplete dominance?(3 votes)
- @7:11did anyone also realise that the results of the wheat example (read pigments) where from Pascal triangle i mean the 1:6:15:20:15:6:1.(3 votes)