Non Mendelian Genetics
Genetics Overview
Understanding traits requires knowledge of specific laws governing inheritance.
Laws of Inheritance
Law of Independent Assortment: Chromosomes align randomly at the metaphase plate, leading to various combinations of maternal and paternal characteristics in offspring.
Law of Segregation: Duplicated chromosomes separate, ensuring only one allele for each trait goes into a gamete, preventing the offspring from getting two alleles for the same trait (e.g., eye color).
Non-Mendelian Genetics
Inheritance can be more complex than Mendelian principles (dominant and recessive traits).
Degrees of Dominance
Incomplete Dominance: Phenotype is a blend of the parents. Example: Black (B) and white (W) rabbits producing gray (BW) offspring.
Codominance: Both dominant traits are expressed fully. Example: Black (B) and white (W) rabbits producing offspring with both black and white fur.
Multiple Alleles
Some traits are controlled by more than two alleles, resulting in various phenotype expressions.
Example: Blood groups with A (IA), B (IB), and O (i) alleles, leading to possible combinations (AA, AB, AO, etc.).
Polygenic Inheritance
Traits controlled by two or more genes, leading to a range of phenotypes.
Examples include height and skin color, where environmental factors also contribute to the expression of these traits.
Sex-Linked Traits
Genes located on the X or Y chromosome. Most sex-linked traits are X-linked due to the larger number of genes on the X chromosome.
Inheritance Pattern
Fathers pass X-linked alleles to daughters but not to sons (sons receive Y from father).
Mothers can pass X-linked alleles to both daughters and sons.
Carrier Status
Carriers have one normal allele and one affected allele for a recessive trait, allowing them to pass on the trait without expressing it themselves.
Males are hemizygous for X-linked traits; they express the trait if they inherit the affected X allele from their mother.
Common X-Linked Disorders
Conditions such as color blindness and hemophilia often appear in inheritance pattern questions.
X Inactivation
During development, one of the X chromosomes in females becomes inactive, forming a Barr body, which regulates gene expression.
The choice of which X is inactivated is random.
Linked Genes
Genes located close together on the same chromosome tend to be inherited together, showing parental phenotypes in higher proportions than recombinant phenotypes.
Recombinant vs. Parental Types
Parental Types: Offspring that resemble the parents.
Recombinant Types: Offspring that do not resemble either parent due to crossing over events during meiosis.
If recombination frequency exceeds 50%, genes are likely on different chromosomes (unlinked).
Genetic Variation Sources
Independent assortment, crossing over during meiosis, and the random fertilization of egg and sperm contribute to genetic diversity.