BackFundamental Principles of Genetics: Mendelian Inheritance, Blood Types, and Genetic Crosses
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Mendelian Genetics
Monohybrid Crosses
Monohybrid crosses examine the inheritance of a single trait controlled by two alleles. This foundational concept in genetics was first described by Gregor Mendel.
One trait with two alleles (e.g., T = tall, t = short).
Cross: Tt × Tt
Genotypes: TT, Tt, tt
Phenotypic ratio: 3 tall : 1 short
Example: Crossing two heterozygous pea plants for height results in three tall plants for every one short plant.
Dihybrid Crosses
Dihybrid crosses involve two traits, each controlled by two alleles. These crosses help illustrate the principle of independent assortment.
Two traits (e.g., seed color Y and shape S).
Cross: YySs × YySs
Punnett Square: Used to determine genetic combinations.
Phenotypic ratio:
9 yellow smooth
3 yellow wrinkled
3 white smooth
1 white wrinkled
Example: Crossing two heterozygous plants for seed color and shape yields a 9:3:3:1 ratio in the offspring.
Patterns of Inheritance
Dominant vs Recessive
Alleles can be classified as dominant or recessive, determining how traits are expressed in offspring.
Dominant: Expressed even if only one allele is present (TT or Tt).
Recessive: Only expressed if both alleles are recessive (tt).
Example: Free earlobes (dominant) vs attached earlobes (recessive).
Codominance
In codominance, both alleles are fully expressed in the phenotype of the heterozygote.
Both alleles are fully expressed.
Example: Black chicken (CB) × White chicken (CW) → CBCW = black and white speckled offspring.
Incomplete Dominance
Incomplete dominance occurs when the heterozygote displays a phenotype intermediate between the two homozygotes.
Alleles blend in heterozygous form.
Example: Red (CR) × White (CW) → CRCW = pink flowers.
X-Linked Recessive Traits
X-linked traits are found on the X chromosome and often show different patterns of inheritance in males and females.
Found on the X chromosome.
Pedigree analysis: Males (XY) more likely to express trait; females (XX) can be carriers.
Example: Color blindness, hemophilia.
Blood Type Inheritance
Genotypes and Phenotypes
Human blood types are determined by three alleles: A, B (codominant), and O (recessive). The combination of these alleles produces four possible blood types.
Alleles: A, B (codominant), O (recessive)
Genotypes and Phenotypes:
Blood Type | Genotype(s) |
|---|---|
A | AA, AO |
B | BB, BO |
AB | AB |
O | OO |
Example: A child with parents of blood types A and B can have any of the four blood types, depending on parental genotypes.
Practice Problems and Answers
Monohybrid Cross
Question: Heterozygous parents mate. What is the phenotypic ratio?
Answer: 3 tall : 1 short
Dihybrid Cross
Question: Heterozygous parents mate. What is the phenotypic ratio?
Answer: 9:3:3:1
Dominant/Recessive
Question: Child has attached earlobes (recessive). Parents have free earlobes. What are the genotypes of the parents?
Answer: Ee × Ee
Codominance
Question: Black and white chicken phenotype?
Answer: Black and white speckled
Incomplete Dominance
Question: Red × white flower. What is the phenotype?
Answer: 100% pink
X-Linked Recessive
Question: Carrier mom × normal dad. What is the chance son is color blind?
Answer: 50%
Blood Type
Question: Heterozygous A mom × heterozygous B dad. What are the possible blood types of children?
Answer: A, B, AB, O
Additional Topics for Review
Mitosis
Meiosis
Nondisjunction and disorders, karyotype
DNA structure, component
Alleles and inheritance:
Dominant vs recessive
Monohybrid cross
Dihybrid cross
Codominance
Incomplete dominance
Multiple alleles
Blood typing
Sex-linked
Pedigree
Additional info: For mitosis and meiosis, students should review the stages and outcomes of each process, as well as their roles in genetic variation. Nondisjunction leads to chromosomal disorders such as Down syndrome. DNA structure includes the double helix, nucleotide components, and base pairing rules.