What are the complementary base pairs in DNA?
Answer: Adenine pairs with thymine; guanine pairs with cytosine.
Explanation
In RNA, uracil replaces thymine.
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What are the complementary base pairs in DNA?
Answer: Adenine pairs with thymine; guanine pairs with cytosine.
In RNA, uracil replaces thymine.
What is a frameshift mutation?
Answer: An insertion or deletion not in multiples of three that shifts the reading frame.
Usually produces a nonfunctional protein.
What is a point mutation, and what kinds exist?
Answer: A change in a single nucleotide: silent (no change), missense (different amino acid), or nonsense (premature stop).
Sickle cell is a missense mutation.
What happens during translation?
Answer: Ribosomes read mRNA codons and tRNAs deliver matching amino acids to build a polypeptide.
Starts at AUG (methionine); stops at UAA, UAG, or UGA.
What happens during transcription?
Answer: RNA polymerase reads the DNA template strand and builds a complementary mRNA.
In eukaryotes, pre-mRNA is capped, polyadenylated, and spliced.
What is the central dogma?
Answer: DNA is transcribed into RNA, which is translated into protein.
Retroviruses reverse the first step with reverse transcriptase.
What do DNA polymerase, helicase, and ligase do in replication?
Answer: Helicase unwinds the double helix; DNA polymerase adds nucleotides to the 3' end; ligase joins Okazaki fragments.
Primase lays down RNA primers first.
Describe semiconservative replication.
Answer: Each new DNA molecule has one original (parental) strand and one newly synthesized strand.
Shown by the Meselson-Stahl experiment.
What does CRISPR-Cas9 do?
Answer: Uses a guide RNA to direct the Cas9 enzyme to cut DNA at a specific sequence, enabling gene editing.
Adapted from a bacterial immune system.
What are restriction enzymes?
Answer: Enzymes that cut DNA at specific recognition sequences, often leaving sticky ends.
Used to insert genes into plasmids.
What is gel electrophoresis used for?
Answer: Separating DNA fragments by size; smaller fragments move farther through the gel toward the positive electrode.
DNA is negatively charged because of its phosphate backbone.
What does PCR do?
Answer: Amplifies a specific DNA segment through repeated cycles of denaturing, annealing primers, and extension.
Uses heat-stable Taq polymerase.
What is epigenetics?
Answer: Heritable changes in gene expression without changes to the DNA sequence, such as DNA methylation and histone modification.
Explains how identical genotypes can differ in expression.
What is the difference between a promoter and an enhancer?
Answer: A promoter is where RNA polymerase binds to start transcription; an enhancer is a distant sequence that increases transcription when bound by activators.
Eukaryotic genes commonly have both.
How does the lac operon work?
Answer: When lactose is absent a repressor blocks transcription; lactose (as allolactose) removes the repressor so the genes are expressed.
An inducible operon; cAMP-CAP boosts expression when glucose is low.
What is Mendel's law of segregation?
Answer: Each organism carries two alleles for a trait, and they separate during gamete formation so each gamete gets one.
Explains 3:1 ratios in monohybrid crosses.
What is a test cross and why is it used?
Answer: Crossing an organism with a dominant phenotype to a homozygous recessive to reveal whether it is homozygous or heterozygous.
If any recessive offspring appear, the parent was heterozygous.
What ratio results from a monohybrid cross of two heterozygotes (Bb × Bb)?
Answer: 3:1 phenotypic, 1:2:1 genotypic.
1 BB : 2 Bb : 1 bb.
Genotype vs phenotype?
Answer: Genotype is the allele combination (e.g., Bb); phenotype is the observable trait (e.g., brown eyes).
Different genotypes can share a phenotype.
What is the law of independent assortment?
Answer: Alleles of different genes assort independently during gamete formation.
Holds for genes on different chromosomes or far apart; gives 9:3:3:1 dihybrid ratios.
What is a Barr body?
Answer: An inactivated X chromosome in female mammalian cells.
X-inactivation is random; calico cat coloring results from it.
What is a karyotype?
Answer: An organized picture of all the chromosomes in a cell, used to detect chromosomal abnormalities.
Humans have 23 pairs (46 total).
What is nondisjunction?
Answer: Failure of chromosomes to separate properly during meiosis, producing gametes with extra or missing chromosomes.
Trisomy 21 (Down syndrome) results from nondisjunction.
What is genetic linkage?
Answer: Genes close together on the same chromosome tend to be inherited together.
Recombination frequency estimates the distance between them (1% = 1 map unit).
What is a sex-linked trait and why are males more often affected?
Answer: A trait on the X chromosome; males have only one X, so a single recessive allele is expressed.
Red-green color blindness and hemophilia are X-linked recessive.
What is polygenic inheritance?
Answer: A trait controlled by many genes, producing continuous variation.
Height and skin color show bell-curve distributions.
What is epistasis?
Answer: One gene's expression masks or modifies the effect of another gene.
Coat color in Labradors: the E gene controls whether the B gene's pigment is deposited.
What is pleiotropy?
Answer: One gene affects multiple phenotypic traits.
Sickle cell allele affects blood, circulation, and malaria resistance.
What is codominance?
Answer: Both alleles are fully expressed in the heterozygote.
AB blood type expresses both A and B antigens.
What is incomplete dominance?
Answer: The heterozygote shows a blended, intermediate phenotype.
Red × white snapdragons → pink.
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