On this page:
Introduction What Is a Gene? Genotype and Phenotype Mendelian Genetics Monohybrid Cross Dihybrid Cross Co-dominance and Incomplete Dominance Multiple Alleles Sex Linked Inheritance Linkage and Crossing Over Polygenic Inheritance Meiosis and Genetic Variation Mutations Examining Family Trees Applications Summary
Have you ever thought about the reason you share your eye color with your parents? Or that some traits appear for a generation and then don't? Inheritance is the process that covers the passing down of genetic information from generation to generation. It is responsible for the reason offspring resemble their parents, and the reason that there is a genetic variation within a population.
A gene is a section of DNA that is responsible for coding either a specific protein or trait of an organism. Genes are organized in structures called chromosomes, which, in turn, are contained in the nucleus of the organism's cells. Organisms inherit genes from their parents. Humans, for example, have a total of 46 chromosomes, which is equivalent to 23 pairs.
Every gene also possesses alternative alleles, referred to as dominant and recessive.
Example:
Refers to the genetic makeup of the organism (which alleles the organism has).
Refers to the traits that are visible as a result of the organism's genotype.
Example: Genotype: Bb (which are brown eyes) Phenotype: brown eyes
A trait can be monogenic, meaning that a single gene controls the trait, or polygenic, meaning that multiple genes control it.
Gregor Mendel, studying pea plants, formulated the basic principles of the law of inheritance.
An organism has two alleles for each gene and as gametes are formed, the alleles for that gene separate. Therefore, each gamete will have an allele either one of the two.
If genes are located on separate chromosomes, they will be inherited independently of each other.
Mendel's laws help to understand inheritance in a dominant and recessive manner.
A monohybrid cross is a genetic cross using one trait. Example: BB would be brown and bb would be blue.
BB x bb
Gametes: B, B and b, b
Offspring: Bb, Bb, Bb, Bb
Phenotype: All brown
Bb x Bb
Phenotype ratio: 3:1
3 Brown : 1 Blue
The F1 generation will only contain the dominant trait. The F2 generation (Bb x Bb) will have a phenotype ratio of 3:1.
A dihybrid cross involves two traits.
Example: Seed shape (R = round, r = wrinkled) and seed color (Y = yellow, y = green)
F1 generation: RrYy × RrYy
F2 generation: 9:3:3:1 phenotypic ratio
Dihybrid crosses demonstrate independent assortment.
The heterozygote has a blended phenotype.
Example: red flower (RR) X white flower (rr) result in pink flower (Rr)
Both alleles are fully expressed.
Example: human blood group AB (IAIB) both a and b antigen appear.
Some genes in a population exhibit more than two alleles.
Example: human ABO blood group. three alleles: IA, IB, i.
IA and IB are co-dominant, i is recessive.
Some genes are located on sex chromosomes, these are X-linked traits.
Example: Red green color blindness is X-linked recessive. A mother, carrier (XcX) and father, normal (XY) may have color blind sons.
Certain traits such as, height, skin color, and intelligence are the result of the influence of multiple genes. Each gene is likely to have a small impact.
The variation observed in these traits is not discrete as it is with traits determined by a single gene.
Example: Offspring can inherit a particular number of height-influencing alleles from their parents, leading to great variation in height.
Meiosis is a unique type of cell division that is responsible for the formation of gametes and also ensures the following:
This explains why siblings look similar but are not identical.
A mutation can be defined as a gene or chromosome change that occurs in the DNA sequence.
A mutation can be good, bad, or neither. If the mutation occurs in a gamete, it can be passed on to future generations.
A family tree can help trace how a family member's genes have changed. The following symbols are used:
A family tree can help identify traits that are:
| Term | Definition |
|---|---|
| Allele | Different form of a gene |
| Dominant | An allele expressed over another |
| Recessive | An allele that is masked by a dominant allele |
| Genotype | Genetic make-up |
| Phenotype | An observable trait |
| Homozygous | Having the same alleles (AA or aa) |
| Heterozygous | Having different alleles (Aa) |
| Linkage | Genes located on the same chromosome |
| Polygenic | Refers to trait controlled by many genes |
| Mutation | Refers to a change in the DNA sequence |
| Sex-linked | Refers to genes located on a sex chromosome |
The essence of genetics is Inheritance. It is vital in understanding how traits are passed on, how variation occurs, and how certain diseases are hereditary. It helps scientists, doctors, and breeders make decisions in agriculture, medicine and research. The study of monohybrid and dihybrid crosses, sex-linked traits, polygenic inheritance, and mutations help students understand the complexity and beauty of genetics in life.