Patterns of Inheritance
Patterns of Inheritance
Focus on different inheritance patterns as discussed in Chapter 9 of genetics.
Mendel’s Dihybrid Crosses
Explored questions regarding whether traits are inherited independently.
Initial Hypothesis: Dependent Assortment
Actual data did not support this hypothesis.
Proposed Hypothesis: Independent Assortment
Data supported this hypothesis.
Mendel’s Law of Independent Assortment
Stated that each pair of alleles segregates independently during gamete formation.
Extensions of Mendel
Incomplete Dominance:
Example: Snapdragons; Red (RR) x White (rr) = Pink (Rr).
Generations:
Parental Generation: RR x rr
F₁ Generation: All pink (Rr)
F₂ Generation: Phenotypic ratio 1:2:1 (1 red: 2 pink: 1 white); Genotypic ratio 1:2:1.
Codominance:
Example: Red x White = both colors expressed (e.g., rhododendron with red and white flowers).
Multiple Alleles and Blood Types
Blood type inheritance exhibits multiple alleles and codominance.
Genotypes for Blood Groups:
Type A: AA or AO
Type B: BB or BO
Type AB: AB
Type O: OO
Carbohydrates on Red Blood Cells:
Carbohydrate A triggers Anti-B antibodies and vice-versa.
Group AB has none, while Type O is neutral (no reaction).
Pleiotropy and Polygenic Inheritance
Pleiotropy:
Single gene affects multiple traits (Example: albinism).
Polygenic Inheritance:
Multiple genes influence one trait, e.g., skin color, resulting in a continuous range (light, medium, dark).
Results in varied phenotypes such as multiple shades of skin tone based on combined alleles.
Nature vs. Nurture
Environmental influences on phenotypic traits.
Epigenetic Inheritance
Traits are transmitted not only via DNA sequences but also through gene expression modifications (chemical changes).
Studying Inheritance Patterns
Use of pedigree charts to track traits and inheritance through generations.
Types of Inheritance
Single-Gene Disorders:
Less common as most traits are polygenic.
Autosomal Dominant:
Traits appear in every generation equally in males and females (e.g., Huntington's Disease).
Autosomal Recessive:
Traits can skip generations; heterozygotes are carriers (e.g., Tay-Sachs).
X-Linked Inheritance:
Seen more in males due to single X chromosome acting as a determining factor (e.g., Duchenne muscular dystrophy, Hemophilia).
Male Sex Determination in Humans
SRY gene's role in male secondary sexual traits emergence.
Sex determination is multifactorial considering chromosomes, genes, and secondary sexual characteristics.
Disorders of sex development (DSD) can lead to various developmental outcomes and gender identity variances, illustrating complexities beyond biological definitions.