Mendels Genetics
Introduction to Mendelian Genetics
Review of Chromosomes
Human cells contain a total of 46 chromosomes.
These chromosomes are composed of DNA that gives each cell its unique identity.
Chromosomes are inherited as follows:
23 chromosomes from the father.
23 chromosomes from the mother.
This inheritance structure indicates that each person possesses a combination of genetic codes from both parents.
The phrase "23 pairs of chromosomes" emphasizes the maternal and paternal copies of each chromosome.
Alleles
Definition of Allele
An allele is defined as a small section on a chromosome that codes for a specific gene that contributes to an individual's uniqueness.
Since humans usually have two copies of each chromosome, they generally possess two alleles for every specific gene (one from each parent).
Example: Blood Type
Explanation of Blood Types
Blood types are traditionally identified by letters, such as A, B, and O.
Each blood type corresponds to specific alleles that determine the blood type's characteristics.
Individual Examples
Male Example:
Alleles code for blood type A (denoted as AA).
Since both alleles are the same (AA), his blood type is confirmed as A.
Female Example:
One allele codes for blood type A and the other for blood type O (denoted as AO).
The presence of one A allele means her blood type will also be A.
Terminology
Homozygous vs. Heterozygous
Homozygous
Definition: An individual with two identical alleles for a particular gene.
Example: The man with AA alleles is considered homozygous.
Etymology: "Homo" means same; "zygos" refers to the mix of DNA from parents.
Heterozygous
Definition: An individual with two different alleles for a particular gene.
Example: The woman with AO alleles is considered heterozygous.
Etymology: "Hetero" means different.
Dominant vs. Recessive Alleles
Dominant Allele: This allele will express its trait even if there is only one copy present.
In the example, the A allele is dominant over the O allele.
Recessive Allele: This allele will only express its trait if two copies are present.
Genotype vs. Phenotype
Definitions
Genotype
Refers to the specific alleles present in an individual.
Example: The man's genotype is AA.
Phenotype
Refers to the observable traits of an individual resulting from the genotype.
Example: The phenotype for both the man and the woman is blood type A.
Relationship Between Genotype and Phenotype
It is possible for different genotypes to lead to the same phenotype due to the dominance of certain alleles.
Gene Inheritance
Introduction to Punnett Squares
A Punnett square is a tool used to predict the genotype and phenotype ratios of offspring from two parents.
Each parent contributes one allele to the offspring, represented in the Punnett square.
Example Scenario: Offspring from a Homozygous Male and Heterozygous Female
Parent Alleles:
Father's alleles (AA) are placed vertically.
Mother's alleles (AO) are placed horizontally.
Resulting Genotypes
Square results in:
2 squares with AA (representing homozygous children).
2 squares with AO (representing heterozygous children).
Phenotype: All children will have blood type A phenotype since both AA and AO code for blood type A.
Scenario Change: Heterozygous Male and Female
If both parents are heterozygous (AO), the Punnett square indicates:
1 square with AA (25% probability).
2 squares with AO (50% probability).
1 square with OO (25% probability).
Outcome:
75% of children will exhibit blood type A phenotype.
25% will exhibit blood type O phenotype.
Summary of Learning Outcomes
Key Concepts Covered
Definition of an allele and the difference between homozygous and heterozygous.
Understanding of dominant vs. recessive traits related to alleles.
Distinction between genotype (genetic makeup) and phenotype (observable traits).
Use of Punnett squares to analyze inheritance patterns and predict offspring traits.