November 2026 - Cell Division & Genetics Study Guide for nursing students in
DNA is a double helix in which adenine pairs with thymine and cytosine with guanine. Genotype is the genetic makeup, phenotype the observable trait, and alleles can be dominant or recessive. Base pairing is the fact most directly tested.
Try 4 short questions throughout this guide. Check each answer to learn from the explanation.
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Genetic information flows from DNA to RNA to protein. During meiosis, homologous chromosomes and then their copies separate so four haploid cells result.
The structure of DNA
A double helix: two strands twisted around each other.
Each strand is a chain of nucleotides, and each nucleotide is a sugar, a phosphate and a base.
The two strands are held together by pairs of bases: A with T, and C with G.
The pairing rule means one strand determines the other exactly, which is what makes copying possible.
DNA and RNA
DNA
RNA
Strands
Double
Single
Sugar
Deoxyribose
Ribose
Bases
A, T, C, G
A, U, C, G — uracil replaces thymine
Where
The nucleus
Made in the nucleus, works in the cytoplasm
Job
Long-term storage of the code
Carrying it to the ribosome and building protein
In RNA, adenine pairs with uracil rather than thymine. A transcription question that offers a T in the RNA answer is testing exactly this, and the choice with a T is always there.
Question 1 of 4
In DNA, which base pairs with cytosine?
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Correct answer: C. Guanine
Cytosine always pairs with guanine, just as adenine pairs with thymine. Uracil appears only in RNA, where it substitutes for thymine — so it never pairs with cytosine in either molecule.
From gene to protein
Three processes, and the exam asks which is which.
DNA
Replication — DNA copied
Transcription — DNA to mRNA
Translation — mRNA to protein
Question 2 of 4
Which process produces a protein from an mRNA sequence?
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Correct answer: C. Translation
Translation is the ribosome reading mRNA and assembling amino acids into a protein. Replication copies DNA, transcription produces the mRNA that translation then reads, and a mutation is a change to the sequence rather than a step in making a protein.
Genotype and phenotype
Genotype is the pair of alleles an individual carries — BB, Bb or bb. Phenotype is what you can observe: the trait that pair produces. Two different genotypes can give the same phenotype, which is the whole reason recessive traits can skip a generation.
An individual with two identical alleles is homozygous; with two different ones, heterozygous. A dominant allele shows in the phenotype whenever it is present, so a recessive trait appears only when both alleles are recessive.
Building a complementary strand
Worked example
A DNA strand reads A-T-G-C-C-A. Give the complementary DNA strand, and the mRNA transcribed from the original.
For DNA, apply A–T and C–G to each base in turn.
A→T, T→A, G→C, C→G, C→G, A→T, giving T-A-C-G-G-T.
For mRNA, apply the same rule but replace thymine with uracil.
A→U, T→A, G→C, C→G, C→G, A→U, giving U-A-C-G-G-U.
Complementary DNA: T-A-C-G-G-T. mRNA: U-A-C-G-G-U. The only difference is U in place of T.
Chromosomes and mutations
Human body cells carry 46 chromosomes in 23 pairs; gametes carry 23.
A gene is a section of DNA coding for a protein; an allele is one version of a gene.
A mutation is a change in the DNA sequence. It may be harmful, beneficial or have no effect at all.
Sex is determined by the 23rd pair: XX or XY.
Terms to know
DNA
The double-helix molecule that stores genetic information.
Nucleotide
The unit of DNA: a sugar, a phosphate and a base.
Base pair
A joined pair of bases: A with T, C with G. In RNA, A with U.
Gene
A section of DNA coding for a protein.
Allele
One version of a gene.
Genotype
The alleles an individual carries.
Phenotype
The observable trait those alleles produce.
Homozygous
Carrying two identical alleles.
Heterozygous
Carrying two different alleles.
Mutation
A change in the DNA sequence.
What the HESI asks most
The same core ideas appear in different wording. If you can answer these without stopping to think, you have what this section requires.
Which base pairs with this one?
A with T, C with G. In RNA, A with U.
What is the difference between genotype and phenotype?
Genotype is the alleles carried; phenotype is the trait you can observe.
What distinguishes RNA from DNA?
Single-stranded, ribose sugar, and uracil in place of thymine.
Which process converts DNA into mRNA?
Transcription. Translation converts mRNA into protein.
Question 3 of 4
A person carries one dominant and one recessive allele for a trait. Which term describes this?
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Correct answer: C. Heterozygous
Two different alleles is heterozygous, and because the dominant allele is present it is the one expressed in the phenotype. Homozygous means both alleles are the same, and "phenotypic" describes the observable trait rather than the genotype.
Key points
DNA is a double helix; A pairs with T and C with G.
RNA is single-stranded and uses uracil instead of thymine.
Replication copies DNA, transcription makes mRNA, translation makes protein.
Genotype is the alleles; phenotype is the observable result.
A recessive trait appears only when both alleles are recessive.
Question 4 of 4
A DNA strand reads T-A-C-G. What is the corresponding mRNA sequence?
Choose one answer, then check it.
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Correct answer: B. A-U-G-C
Applying complementary pairing gives A, U, G, C — with uracil replacing the thymine that DNA would use. A-T-G-C is the complementary DNA strand rather than the RNA, and the last two choices copy the original instead of complementing it.
HESI · Cell division and genetics
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