Mendel&Gene_Mendelian_genetics_part1
Mendel and Genetics Overview
Heredity: Transmission of traits from one generation to the next.
Gregor Mendel: Published the theory of "Particulate Inheritance" in 1865; ignored initially, rediscovered in 1902.
Historical Context
Before Mendel: Concept of Blending Inheritance where traits mix evenly (e.g., red and white horses produce roan).
Mendel's Model Organism
Garden Pea (Pisum sativum): A hermaphroditic plant with both male and female reproductive organs.
Fertilization Techniques
Self-fertilization: Female organs receive pollen from the same plant.
Cross-fertilization:
Pollen is collected from one plant and transferred to the female organ of another plant, whose male organs have been removed.
Mendel's Experiments & Generations
P Generation: True-breeding parents (e.g., purple and white flowers).
F1 Generation: All offspring display the dominant trait (purple flowers).
F2 Generation: Resulting ratio of traits:
3/4 purple flowers
1/4 white flowers
Key Concepts in Mendelian Genetics
Each plant has two hereditary factors (alleles): dominant (P) and recessive (p).
Only one allele from each parent is passed to the offspring.
Dominance hierarchy:
Dominant allele leads to purple flowers (presence of P).
Recessive allele leads to white flowers (absence of P).
Punnett Square Analysis
Monohybrid Cross: Examines inheritance of one trait.
Example: PP (purple) x pp (white) results in 100% Pp (purple).
In F2 generation:
Genotype ratio: 1 PP : 2 Pp : 1 pp
Phenotype ratio: 3 purple : 1 white.
Mendel's Monohybrid Crosses
Investigated traits like seed shape:
Dominant: Round (R)
Recessive: Wrinkled (r)
Phenotype Ratio: 3 round : 1 wrinkled.
Genotype Ratio: 1 RR : 2 Rr : 1 rr.
Further Applications of Mendel's Laws
Law of Segregation:
Genes exist in alternative versions called alleles.
Each organism inherits two alleles, one from each parent.
If the alleles differ, the dominant allele dictates the organism's appearance.
Testcross Definition
A testcross involves mating an individual of unknown genotype with a homozygous recessive individual. This reveals whether the unknown genotype carries a recessive allele.