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AP Biology: Genetics and Heredity — quiz
18 multiple-choice questions covering DNA/RNA base pairing, Frameshift mutations, Point mutations, Translation, DNA replication. One answer each; you get a score at the end and the explanation for every question. No account needed.
Updated 2026-10-24. Keys 1–4 pick an answer, Enter moves on. Redo it any time, in order or shuffled.
The questions
Answers and explanations are shown after you finish.
- DNA/RNA base pairing
A DNA template strand reads 3'-TACGGA-5'. What mRNA sequence would be transcribed from it?
- 5'-AUGCCT-3'
- 5'-ATGCCT-3'
- 5'-UACGGA-3'
- 5'-AUGCCU-3'
- Frameshift mutations
A single nucleotide is deleted near the beginning of a gene's coding sequence. What is the most likely effect on the resulting protein?
- A premature stop codon appears immediately at the deletion site only
- A shift in the reading frame scrambles most of the downstream amino acid sequence
- A single amino acid is swapped for another, but the protein still works
- No change, because the deletion is outside the gene
- Point mutations
A point mutation changes the codon UAC (tyrosine) into UAA. What type of mutation is this?
- Nonsense mutation
- Silent mutation
- Missense mutation
- Frameshift mutation
- Translation
During translation, what directly signals the ribosome to release the finished polypeptide?
- The ribosome reaching the 5' cap of the mRNA
- A tRNA bringing a stop amino acid
- The ribosome encountering a stop codon such as UAA
- The poly-A tail binding the ribosome
- DNA replication
On the lagging strand, DNA is synthesized in short Okazaki fragments. Which enzyme seals the gaps between these fragments into a continuous strand?
- Primase
- Helicase
- DNA ligase
- DNA polymerase
- CRISPR-Cas9
In CRISPR-Cas9 gene editing, what role does the guide RNA play?
- It serves as a primer that DNA polymerase extends
- It is translated into the Cas9 protein itself
- It repairs the DNA break after Cas9 cuts it
- It directs the Cas9 enzyme to the specific DNA sequence to be cut
- Gel electrophoresis
A researcher runs a gel with DNA fragments of 200 bp, 500 bp, and 1000 bp. Which fragment migrates farthest toward the positive electrode?
- The 200 bp fragment, because smaller fragments move faster through the gel
- The 500 bp fragment, because it is intermediate in size
- All fragments move the same distance since DNA charge density is constant
- The 1000 bp fragment, because it has more charge
- Epigenetics
Identical twins share the same DNA sequence, yet one develops a disease linked to a silenced tumor-suppressor gene while the other does not. What best explains this difference?
- The twins actually have different alleles at that locus
- Epigenetic changes such as DNA methylation altered gene expression without changing the sequence
- Differences in mRNA codon usage changed the protein produced
- One twin has a unique mutation the other lacks
- Lac operon regulation
In E. coli, both lactose and glucose are present in high amounts. Compared to when lactose is present but glucose is absent, lac operon transcription will be...
- Lower, because low cAMP means CAP cannot strongly activate the promoter
- Unaffected, since glucose has no influence on the lac operon
- Higher, because both sugars together maximize activation
- Completely shut off by the lac repressor
- Test crosses
A purple-flowered pea plant is crossed with a white-flowered plant, and the offspring are 50% purple and 50% white. What does this reveal about the purple parent's genotype?
- It is homozygous dominant (PP)
- It is homozygous recessive (pp)
- Its genotype cannot be determined from this cross
- It is heterozygous (Pp)
- Independent assortment
Two pea plants, each heterozygous for seed shape and seed color (RrYy), are crossed. Assuming independent assortment, what phenotypic ratio is expected in the offspring?
- 1:2:1
- 3:1
- 9:3:3:1
- 1:1:1:1
- Genotype vs phenotype
Two pea plants both display red flowers, but one has genotype RR and the other has genotype Rr. This best illustrates that...
- Different genotypes can produce the same phenotype
- Incomplete dominance is occurring
- The red allele is recessive
- Phenotype always reveals the exact genotype
- Nondisjunction
A gamete is found to contain 24 chromosomes instead of the normal 23 because a homologous pair failed to separate during meiosis I. This error is called...
- Polyploidy
- Crossing over
- Nondisjunction
- Translocation
- Sex-linked inheritance
A woman who is an unaffected carrier for an X-linked recessive disorder has sons with a 50% chance of being affected, while her daughters are rarely affected. Why are sons at higher risk?
- The Y chromosome carries a dominant allele that worsens the disorder
- Males have two copies of the gene, doubling their risk
- Daughters inherit the disorder only from their father
- Males have only one X chromosome, so a single recessive allele is expressed
- X-inactivation / Barr bodies
Calico cats display patches of orange and black fur. This pattern is best explained by which process?
- Two separate genes controlling fur color on different chromosomes
- Environmental temperature affecting pigment genes during development
- Incomplete dominance blending orange and black pigments
- Random inactivation of one X chromosome in each cell, forming a Barr body
- Epistasis
In Labrador retrievers, dogs with genotype ee are yellow regardless of whether their B gene would otherwise produce black or brown pigment. This relationship between the E and B genes is an example of...
- Incomplete dominance
- Pleiotropy
- Epistasis
- Codominance
- Codominance vs incomplete dominance
Which scenario best demonstrates codominance rather than incomplete dominance?
- A red snapdragon crossed with a white one produces pink offspring
- A heterozygous pea plant shows a blended intermediate seed color
- Mixing two paint colors produces a new, uniform shade
- A person with genotype IAIB has both A and B antigens fully expressed on their red blood cells
- Pleiotropy
The sickle cell allele changes red blood cell shape, affects oxygen-carrying capacity, and also provides some resistance to malaria. This wide-ranging effect of a single gene is called...
- Polygenic inheritance
- Epistasis
- Codominance
- Pleiotropy
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