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Reading Time: 6 min
Last Updated: March 19, 2026
Main Ideas: 6
Reading Time: 6 min
Last Updated: March 19, 2026
Main Ideas: 6

Topic 5.3 Notes – Mendelian Genetics

Verified for 2027 AP® Biology Exam
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Explains how traits are inherited through the movement of alleles during meiosis and fertilization. Mendel’s laws describe predictable patterns when genes are on different chromosomes. This topic connects cell division, probability, and observable inheritance patterns like autosomal and sex-linked traits.

1. What Mendelian Inheritance Is

Mendelian inheritance describes how alleles move from parents to offspring.

First, the core vocabulary needs to be solid:

  • Gene = segment of DNA that codes for a trait
  • Alleles = different versions of the same gene (A vs a)
  • Genotype = allele combination (AA, Aa, aa)
    • Homozygous = same alleles (AA or aa)
    • Heterozygous = different alleles (Aa)
  • Phenotype = observable trait
  • Dominant allele = expressed if at least one copy is present
  • Recessive allele = expressed only if homozygous

Now connect this to meiosis:

  • Homologous chromosomes separate in meiosis I
  • Each gamete gets one allele per gene (haploid)
  • Fertilization fuses two haploid gametes → restores diploid number
  • This creates new allele combinations, increasing genetic variation

That separation during meiosis leads directly to Mendel’s laws.

2. Mendel’s Two Laws

Law of Segregation

Each organism has two alleles for a gene. Those alleles separate during gamete formation, so each gamete carries only one.

If a parent is Aa:

  • 50% of gametes carry A
  • 50% carry a

When fertilization happens, alleles pair up again randomly.

This explains why Aa × Aa gives a 1 AA : 2 Aa : 1 aa genotypic ratio.

Students often forget this law is literally describing what homologous chromosomes do in meiosis I.

Law of Independent Assortment

Genes on different chromosomes assort independently during meiosis.

If a parent is AaBb, possible gametes are:

  • AB
  • Ab
  • aB
  • ab

All equally likely.

Important limit: this applies to genes on different chromosomes (or far apart on the same one). If genes are linked, this ratio changes.

3. Types of Genetic Crosses and Expected Ratios

Monohybrid Cross

Example: Aa × Aa

Each parent produces gametes A and a, leading to four possible offspring genotypes.

Results:

  • Genotype ratio: 1 AA : 2 Aa : 1 aa
  • Phenotype ratio: 3 dominant : 1 recessive

On tests, they often give phenotype counts and expect you to infer whether the parents were heterozygous.

Dihybrid Cross

Example: AaBb × AaBb (unlinked genes)

Study guide illustration

Dihybrid Punnett square (AaBb × AaBb)

Each parent produces four gametes: AB, Ab, aB, and ab. The 4 × 4 grid shows all 16 genotype combinations.

Phenotypic ratio:

  • 9 A_B_
  • 3 A_bb
  • 3 aaB_
  • 1 aabb

The 9:3:3:1 ratio only works if genes assort independently.

Test Cross

Used to determine genotype of an individual with a dominant phenotype.

Cross unknown (A_) with aa.

  • If any offspring are recessive → unknown is Aa
  • If all offspring are dominant → likely AA

This shows up a lot in FRQs where you must justify genotype from offspring data.

4. Probability Rules in Genetics

Punnett squares are visual tools. Probability rules are faster once you understand them.

Multiplication Rule (Independent Events)

If events are independent:

P(A and B)=P(A)×P(B) P(A \text{ and } B) = P(A) \times P(B)

Example: AaBb × AaBb
Probability of aa = 1/4
Probability of bb = 1/4

Probability of aabb:
14×14=116 \frac{1}{4} \times \frac{1}{4} = \frac{1}{16}

Addition Rule (Mutually Exclusive Events)

If events cannot happen at the same time:

P(A or B)=P(A)+P(B) P(A \text{ or } B) = P(A) + P(B)

Example: dominant phenotype in Aa × Aa
AA or Aa
14+12=34 \frac{1}{4} + \frac{1}{2} = \frac{3}{4}

On exams, they love asking about probability across multiple children. Each child is an independent event.

5. Patterns of Inheritance and How to Recognize Them

Autosomal Inheritance

  • Gene on non-sex chromosome
  • Males and females equally affected

Pedigree clue: equal distribution across sexes.

Sex-Linked Inheritance (Usually X-linked)

  • Gene on X chromosome
  • Males (XY) express recessive traits more often
  • No father-to-son transmission (for X-linked traits)

If you see mostly affected males in a pedigree, think X-linked recessive.

Genetically Linked Genes

  • Located on same chromosome
  • Do not assort independently
  • Inherited together more often than expected
  • Crossing over can separate them

If offspring ratios deviate from 9:3:3:1, linkage is a possibility.

Big Picture Connection

Mendel’s laws explain inheritance for genes on different chromosomes.
Meiosis (segregation + independent assortment) and random fertilization generate variation.
That variation is the raw material for evolution, tying this topic back to Big Idea 1.

Key Takeaways

Law of segregation describes homologous chromosomes separating in meiosis I.
Independent assortment only applies to genes on different chromosomes.
A 3:1 ratio usually signals a heterozygous monohybrid cross.
The 9:3:3:1 ratio only works for unlinked genes.
Use P(A and B)=P(A)×P(B)P(A \text{ and } B) = P(A)\times P(B) for independent traits and P(A or B)=P(A)+P(B)P(A \text{ or } B) = P(A)+P(B) for mutually exclusive genotypes.
No father-to-son transmission strongly suggests X-linked inheritance.
If observed ratios deviate from expected Mendelian ratios, consider genetic linkage.

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Notes

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