Dominant Inheritance When a trait is dominant, only one allele is required for the trait to be observed. A dominant allele will mask a recessive allele, if present. A dominant allele is denoted by a capital letter (A versus a). Since each parent provides one allele, the possible combinations are: AA, Aa, and aa. Offspring whose genotype is either AA or Aa will have the dominant trait expressed phenotypically, while aa individuals express the recessive trait. One example of a dominantly inherited trait is the presence of a widow’s peak (a V-shape) at the hairline. Let (W) represent the dominant allele, and (w) represent the recessive allele. An individual with a (WW) or (Ww) genotype will have a V-shaped peak at the hairline. Only ww individuals will have a straight hairline. To determine the probability of inheritance of a widow’s peak (or any other dominant trait), the genotypes of the parents must be considered. For example, if one parent is homozygous dominant (WW) and the other is homozygous recessive (ww), then all their offspring will be heterozygous (Ww) and possess a widow’s peak. If both parents are heterozygous (Ww), there is a 75% chance that any one of their offspring will have a widow’s peak (see figure). A Punnett square can be used to determine all possible genotypic combinations in the parents.Pedigree A pedigree that depicts a dominantly inherited trait has a few key distinctions. Every affected individual must have an affected parent. Dominantly inherited traits do not skip generations. Lastly, males and females are equally likely to receive a dominant allele and express the trait. In this pedigree both heterozygous and homozygous individuals are affected since the trait is dominant. Image courtesy of Michael A. Kahn, DDSCLICK HERE to learn more about patterns of inheritance
In order to continue enjoying our site, we ask that you confirm your identity as a human. Thank you very much for your cooperation. Homozygous refers to the state or condition that occurs when an individual inherits the same DNA sequence for a certain gene from both biological parents. When a particular gene has identical alleles (versions) of chromosomes inherited from both parents, the gene is homozygous. A homozygous trait is referred to by two capital letters (XX) for a dominant trait, and two lowercase letters (xx) for a recessive trait. Biological parents pass on versions of genes to their children. These versions are referred to as alleles. When the alleles are identical, the gene is said to be homozygous. This can lead to a person exhibiting homozygous traits. There are many examples of homozygous genes. Homozygous genes can impact the appearance of a person’s eyes as well as medical conditions related to the eyes.
Homozygous genes can manifest in certain factors that impact a person’s appearance, including hair and skin.
Homozygous genes can predispose a person to develop or have immunity to certain medical conditions.
Homozygous genes can impact a person’s musculoskeletal system, impacting factors related to their movement and appearance.
While the basic homozygous definition simply describes the word as being a descriptive term for a cell that has two identical copies of a gene, the scientific definition is a bit more complex:
In order to interpret the scientific definition, a person will need to know the meaning of some other key scientific terms.
Why do siblings look different even when they have the same parents? The difference lies in their genes – and specifically, whether they have homozygous or heterozygous traits. Keep reading to learn what the difference between these traits are, and what exactly they can determine. To understand homozygous and heterozygous traits, you need to know about the basics of genetics and genotypes. All genotypes consist of two alleles – one from the first parent, and one from the second parent. The combination of these alleles determines whether the offspring exhibits homozygous or heterozygous traits. The difference between these traits is:
Whether a trait is homozygous or heterozygous determines how the offspring exhibits that trait. If both parents have a trait, their offspring is more likely to have it as well. However, only a look at the individual’s DNA can determine their likelihood of exhibiting a particular trait. Homozygous means “same genes received during the zygote period of development.” An individual with homozygous traits received one copy of each allele from each parent. These alleles can either be dominant or recessive. You may see homozygous traits in the following situations:
Homozygous traits don’t always mean that offspring look exactly like their parents. However, if a parent has homozygous traits, it’s more likely that their offspring will resemble them. Check out more examples of homozygous traits with an educational article. Genetics get a bit more complicated when it comes to heterozygous, or “different genetic” traits. Offspring who receive a dominant allele from one parent and a recessive allele from the other parent will exhibit heterozygous traits. That’s why siblings with the same parents sometimes look very different from each other: they received different combinations of genes. Here are some examples of how offspring can exhibit heterozygous traits:
As you can see, heterozygous traits allow for greater genetic variation. They can also protect offspring from gene mutation and possibly harmful genetic disorders. The alleles that offspring receives from its parents can determine what happens to its genetic line for generations to come. Life seems so random and unpredictable sometimes. However, understanding the study of genetics helps us understand more about how life works. To learn more about the details of genotypes and genetic traits, read an article that details the occurrence of codominance in genetics. Then, explore some examples of inherited traits.
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