DNA — Interactive Lab

For middle-school students Chapter 1 of 15 3D Model
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🎨 Color key

Adenine (A) ↔ T
Thymine (T) ↔ A
Guanine (G) ↔ C
Cytosine (C) ↔ G
Backbone

🧬 DNA Double Helix

Drag the model with your mouse or your finger. Use the scroll wheel or the buttons to zoom.

The double helix is made of two strands of nucleotides, joined together by hydrogen bonds between complementary bases.

🧬 What is DNA?

DNA (Deoxyribonucleic Acid) is the molecule that holds the "instructions" for building and running every living organism. Think of it as your body's "instruction book"!
📏
2 meters
of DNA in every cell
🔢
3 billion
base pairs
across a full set of 23 chromosomes
🧫
37 trillion
cells in the body
👥
99.9%
identical DNA between people

🏠 Where is it?

DNA is mostly found in the nucleus of each of our cells, packed into structures called chromosomes. We have 46 chromosomes (23 pairs) — 23 from our mother and 23 from our father!

📝 What does it do?

DNA holds the instructions your body needs to make proteins - the "tools" that do almost everything in your body: from the color of your eyes to the way you digest your food!

💡 Did you know?

If you unwound all the DNA from every cell in your body and laid it out in one line, it would reach from the Earth to the Sun and back about 250 times!

Do the math yourself: 37 trillion cells × 2 meters = 74 billion kilometers of DNA. The Earth is about 150 million km from the Sun, so a round trip is about 300 million km.

🔬 The Structure of DNA

DNA has the shape of a double helix - like a twisted ladder! It was discovered in 1953 by Watson and Crick.

🪜 The parts of the "ladder"

The sides (backbone): Made of sugar (deoxyribose) and phosphate groups — they give it stability.

The rungs: The nitrogen bases that pair up with each other!

🎨 The 4 Bases

DNA uses only 4 "letters" to write all the instructions for life:

  • Adenine (A) - Always pairs with Thymine
  • Thymine (T) - Always pairs with Adenine
  • Guanine (G) - Always pairs with Cytosine
  • Cytosine (C) - Always pairs with Guanine
⚠️ Pairing Rule

A ↔ T (2 hydrogen bonds)
G ↔ C (3 hydrogen bonds)

That's why G-C is more stable!

📐 Dimensions

Feature Value
Helix diameter 2 nanometers (nm)
Distance between bases 0.34 nm
Bases per turn 10 pairs
Height of one turn 3.4 nm

🔗 Base Complementarity & DNA-RNA Differences

The nitrogenous bases are the "letters" of the genetic code. Their complementarity is the key to replication and transcription!

🎨 The Four Bases of DNA

Base Pairing in DNA
A
T
← 2 hydrogen bonds
G
C
← 3 hydrogen bonds

📏 Chargaff's Rules

Erwin Chargaff discovered that in every DNA molecule:

  • The amount of Adenine (A) = the amount of Thymine (T)
  • The amount of Guanine (G) = the amount of Cytosine (C)
  • So: A + G = T + C (purines = pyrimidines)
🔬 Purines vs Pyrimidines

Purines (2 rings): Adenine (A), Guanine (G)
Pyrimidines (1 ring): Thymine (T), Cytosine (C), Uracil (U)

⚖️ Differences Between DNA and RNA

DNA - RNA Comparison

🧬 DNA

Deoxyribonucleic Acid

  • Sugar: Deoxyribose
  • Bases: A, T, G, C
  • Structure: Double-stranded (double helix)
  • Location: Nucleus
  • Function: Information storage
  • Stability: Very stable

📜 RNA

Ribonucleic Acid

  • Sugar: Ribose
  • Bases: A, U, G, C
  • Structure: Single-stranded
  • Location: Nucleus & Cytoplasm
  • Function: Transfer & expression
  • Stability: Less stable
Base Pairing in RNA
A
U
← Uracil instead of Thymine!
G
C
← Same as DNA

📋 Types of RNA

  • mRNA (messenger): Carries the information from DNA to the ribosomes
  • tRNA (transfer): Carries amino acids for protein synthesis
  • rRNA (ribosomal): Structural component of the ribosomes
💡 Why Uracil?

RNA uses Uracil (U) instead of Thymine. Thymine is more stable and protects DNA from mutations, while RNA is a temporary molecule that doesn't need that much stability.

🧫 Chromosomes & Karyotypes

Chromosomes are organized structures of DNA and proteins. The karyotype is the picture of all the chromosomes of an organism!
Chromosome Structure

Centromere - the point where the sister chromatids join

Chromatids - the two identical copies

📊 Human Chromosomes

Type Number Description
Autosomes 44 (22 pairs) Determine body traits
Sex chromosomes 2 (1 pair) XX = female, XY = male
Total 46 23 homologous pairs
Human Karyotype — 22 autosome pairs + 1 sex chromosome pair

Every person has 46 chromosomes. The 23rd pair is either XX or XY — here we show both cases together so you can compare them.

1
2
3
4-5
6-12
13-15
16-18
19-22
XX ♀
XY ♂

🔬 Homologous Chromosomes

Homologous chromosomes are pairs of chromosomes (one from each parent) that:

  • Have the same size and shape
  • Carry the same genes in the same spots (loci)
  • Can have different alleles of the same gene
⚠️ Chromosome Abnormalities

Trisomy 21 (Down syndrome): 3 copies of chromosome 21 (47 chromosomes)
Turner syndrome (XO): Only one X in females (45 chromosomes)
Klinefelter syndrome (XXY): An extra X in males (47 chromosomes)

📦 DNA Packaging

How do 2 meters of DNA fit inside a nucleus only a few micrometers wide?

1
Nucleosomes

DNA wraps around histone proteins (like thread around spools)

2
Chromatin

The nucleosomes form a chromatin fiber 30nm wide

3
Chromosome

During cell division, the chromatin condenses into visible chromosomes

👤 Human Genetic Information

A person's genetic information is stored in DNA, organized into chromosomes, inherited through gametes, and expressed through proteins.
The Cell and Genetic Information
🧬
Cell membrane
Cytoplasm
Nucleus (DNA)
🔢
6×10⁹
base pairs per cell
(2 × 3×10⁹ — one set from each parent)
📏
~2 meters
DNA length/cell
🧬
~20,000
genes
🔬
~5 μm
nucleus diameter

🧫 Body Cells, Gametes & Zygote

From Gametes to the Zygote
🥚
Egg cell
22 + X
n = 23
+
🔵
Sperm cell
22 + X or 22 + Y
n = 23
=
🧬
Zygote
44 + XX or 44 + XY
2n = 46

🔵 Diploid Cells (2n)

Body cells

  • 46 chromosomes
  • 23 homologous pairs
  • They divide by mitosis
  • E.g. skin, muscle and nerve cells

🟢 Haploid Cells (n)

Gametes

  • 23 chromosomes
  • One from each pair
  • They are made by meiosis
  • Egg cells (22+X), Sperm cells (22+X or 22+Y)

📖 Genes and Alleles

🧬 What Is a Gene?

A gene is a piece of DNA that holds the instructions for building a protein. It sits at a specific spot (locus) on the chromosome.

Alleles on Homologous Chromosomes
A
B

From the mother

a
b

From the father

Genotype: Aa, Bb (heterozygous for two genes)

🎭 Types of Alleles

Type Description Example
Dominant (A) Always shows up when it is there Brown eyes
Recessive (a) Shows up only when homozygous Blue eyes
Homozygous Same alleles (AA or aa) Pure line
Heterozygous Different alleles (Aa) Hybrid

🔄 From DNA to Proteins

Gene Expression — The Central Dogma
DNA
Storage
Transcription
mRNA
Transport
Translation
Protein
Function

1️⃣ Transcription (DNA → RNA)

  • Happens in the nucleus
  • RNA polymerase reads the DNA
  • This creates mRNA
  • A→U, T→A, G→C, C→G

2️⃣ Translation (RNA → Protein)

  • Happens in the ribosomes
  • The mRNA is read 3 bases at a time (codons)
  • Each codon = 1 amino acid
  • 20 amino acids, 64 codons
📝 Summary — Human Genetic Information

✓ It is stored in DNA
✓ It is organized into 46 chromosomes
✓ It is inherited through the gametes (23 from each parent)
✓ It is expressed through the making of proteins
✓ It determines the structure and function of the organism

🔄 DNA Replication

Before a cell divides, it has to copy its DNA. The process is semiconservative - every new molecule has one old strand and one new one!

📋 Steps of Replication

1
Unwinding

The enzyme helicase "opens" the double helix, breaking the hydrogen bonds between the bases.

2
Building the starter pieces (primers)

Primase makes small pieces of RNA that work as starting points.

3
Elongation

DNA polymerase reads the old strand and adds the correct complementary bases.

4
Proofreading

Special enzymes check for mistakes and fix them. After all the checks, only about 1 mistake per 1 billion bases is left — 99.9999999% accuracy!

⚡ Speed

DNA polymerase adds about 1000 nucleotides per second in bacteria! In humans it is slower (~50 per second) but more accurate.

🔀 Problems & Solutions

Problem: DNA polymerase only works in one direction (5' → 3').

Solution: One strand (the leading strand) is built non-stop, while the other (the lagging strand) is built in pieces (Okazaki fragments) that are then joined together by ligase!

📖 Genes & Chromosomes

Genes are specific pieces of DNA that hold the instructions for a protein or an RNA. They are the units of heredity!

🧮 Numbers

Item Amount
Chromosomes 46 (23 pairs)
Genes ~20,000
Coding DNA ~1.5% of the total
Base pairs ~3 billion

🧬 From DNA to Protein

Here is how the information flows:

DNA → RNAProtein

Transcription: DNA is copied into RNA

Translation: The RNA is "read" to build a protein

🔤 The Genetic Code

Every triplet of bases (codon) matches one amino acid:

  • AUG → Methionine (start signal)
  • UUU → Phenylalanine
  • UAA, UAG, UGA → stop codons (end signal)

There are 64 codons for only 20 amino acids — the code is "degenerate"!

🎯 Important

98.5% of your DNA does not code for proteins! This "non-coding" DNA controls when and where genes get switched on.

🎭 Genetic Polymorphisms

Polymorphisms are normal differences in the DNA from person to person. They are the reason we are not all the same!

❓ What exactly are they?

Polymorphism = a spot in the DNA where 2 or more versions (alleles) exist in the population, with the rarest one showing up in >1% of people.

📊 Types of Polymorphisms

  • SNP (Single Nucleotide Polymorphism): A change in a single letter. E.g. ...AAGCTAA... vs ...AAGCCAA... - The most common type!
  • Insertions & deletions (indels): Small pieces of DNA that get added or removed
  • STRs (Short Tandem Repeats): Repeats of short sequences. E.g. CAGCAGCAG... - These are used in DNA tests!
  • CNVs (Copy Number Variations): Differences in the number of copies of large pieces
📈 Stats

• There are about 10 million SNPs in the human genome
• Each person has about 4-5 million SNPs
• Two random people differ in ~1/1000 bases

🎯 Why do they matter?

  • Traits: Eye color, hair color, height, blood type
  • Health: Risk of disease, how you react to medicines
  • Identification: Forensics, paternity tests
  • Ancestry: Genealogy tests, population studies

🧪 Example: Blood Types

The ABO gene has 3 alleles: IA, IB, i

Combinations → Blood types:
IAIA or IAi → A | IBIB or IBi → B | IAIBAB | ii → O

⚡ Mutations

Mutations are permanent changes in the DNA sequence. They can be helpful, harmful, or neutral!

🔄 Mutation vs Polymorphism

Mutation Polymorphism
Rare (<1%) Common (>1%)
Often harmful Usually neutral
Appeared recently Old in the population

📝 Types of Mutations

Mutations fall into two big categories:

1️⃣ Point mutationsone base changes. Depending on what that does to the protein, they split into:

  • Silent: the amino acid doesn't change (because the code is degenerate) → no effect at all
  • Missense: a different amino acid goes in → the protein may work less well
  • Nonsense: an early stop codon appears → a cut-short protein that usually doesn't work

2️⃣ Frameshift mutationsinsertion or deletion of bases:

  • Reading frame shift: if the number of bases inserted or deleted isn't a multiple of 3, the whole reading shifts from that point on → every amino acid after it changes!
🔍 Notice the difference

A "point mutation" isn't a fourth type sitting next to the others — it's the category that contains silent, missense and nonsense.

🔥 Causes of Mutations

  • Spontaneous: Mistakes during replication (~1/109 bases)
  • UV radiation: Creates thymine dimers
  • Chemicals: Smoke, certain chemical substances
  • Ionizing radiation: X-rays, gamma rays
🧬 Famous Mutations

Sickle cell anemia: A single change (GAG→GTG) in the hemoglobin gene swaps one amino acid and causes a serious disease.

✅ Repair Mechanisms

The cell has "repair crews" that fix the damage:

  • Checking during replication (proofreading): DNA polymerase checks every base it puts in
  • Repair of mismatched bases (mismatch repair): Spots wrong pairings after replication
  • Repair by cutting out (excision repair): Cuts out and replaces damaged sections

📜 History of the Discovery

The discovery of DNA is a fascinating story of scientific progress that changed the world!
1866
Gregor Mendel
Publishes the laws of heredity from his experiments with pea plants — without knowing anything about DNA! His work was ignored for 34 years.
1869
Friedrich Miescher
Discovers "nuclein" — an unknown substance inside the nuclei of cells. He had no idea how important it was!
1900
Mendel Rediscovered
Three scientists working separately (de Vries, Correns, Tschermak) reach the same conclusions and bring Mendel's forgotten work back into the light. Genetics is born.
1928
Frederick Griffith
The "transformation" experiment with pneumococcus bacteria shows that something carries genetic information.
1944
Avery, MacLeod & McCarty
They prove that DNA (not proteins) is the genetic material!
1950
Erwin Chargaff
Discovers "Chargaff's rules": A=T and G=C in every DNA.
1952
Rosalind Franklin
Perfects the X-ray diffraction method on DNA and leads the work that produced "Photo 51" (it was taken by her doctoral student Raymond Gosling). From it she worked out the dimensions of the helix — the crucial proof of the structure.
1953
Watson & Crick
Using Franklin's X-ray data among other evidence, they propose the double helix model. The 1962 Nobel Prize was shared by Watson, Crick and Wilkins.
2003
Human Genome Project
The sequencing of the human genome is completed — 13 years, $3 billion!
2012
CRISPR-Cas9
Doudna & Charpentier develop the revolutionary DNA editing technique. Nobel Prize 2020!
💔 The forgotten heroine

Rosalind Franklin died of cancer in 1958, without ever getting the recognition she deserved. Her work was crucial to the discovery!

🔗 From the Cell to Proteins

Life is organized in levels! Let's see how we get from the cell all the way to the proteins - the tools of life.

🏛️ The 5 Levels of Organization

1
🧫 Cell

The basic unit of life. Every living organism is made of one or more cells. The human body has about 37 trillion cells!

2
🟣 Nucleus

The "control center" of the cell. It holds the genetic material (DNA) and controls everything the cell does. It's wrapped in a double membrane with pores.

3
🧬 DNA (Chromosomes)

The molecule of heredity. Inside the nucleus, DNA is organized into 46 chromosomes (23 pairs). It holds all the instructions for life!

4
📖 Genes

Sections of DNA that hold the instructions for one protein. We have about 20,000 genes. Each gene is like a "recipe"!

5
🔧 Proteins

The "tools" that do the work! Enzymes, hormones, antibodies, building blocks — they're all proteins. They're made from amino acids.

📊 Size Comparison

Cell: ~10-100 μm (micrometers)
Nucleus: ~5-10 μm
Chromosome: ~1-10 μm (length)
DNA (diameter): ~2 nm (nanometers)
Protein: ~2-10 nm

🔬 Types of Cells

Eukaryotic Prokaryotic
They have a nucleus with a membrane They have no organized nucleus
Animals, plants, fungi Bacteria, archaea
Complex organelles Simpler structure
DNA in chromosomes Circular DNA

🧫 Organelles of the Cell

  • Nucleus: Holds the DNA, controls the cell
  • Mitochondria: "Power plants" — they make ATP
  • Ribosomes: They build the proteins
  • Endoplasmic Reticulum: Transport and processing
  • Golgi Apparatus: "Post office" — it packages proteins
  • Lysosomes: "Digestive system" — they break materials down

🔄 The Flow of Genetic Information

DNA ──transcription──▶ RNA ──translation──▶ PROTEIN

This is the "Central Dogma" of Molecular Biology!

💡 Remember!

Cell → contains → Nucleus → contains → Chromosomes → are made of → DNA → contains → Genes → code for → Proteins

🌱 Mendel's Laws

Gregor Mendel (1822-1884) was an Austrian monk who discovered the basic laws of inheritance by studying pea plants. He is considered the "father of Genetics"!

🔬 Mendel's Experiment

Mendel crossed pea plants that had different traits:

  • Seed color: Yellow vs Green
  • Seed shape: Round vs Wrinkled
  • Plant height: Tall vs Short
  • Flower color: Purple vs White

📜 The 3 Laws

1️⃣ Law of Dominance (Uniformity)

When you cross two pure lines with different alleles for a trait, all the offspring of the first generation (F1) are the same and show the dominant trait.

Example: AA × aa → All Aa (dominant phenotype)

2️⃣ Law of Segregation

When gametes are made, the two alleles of a gene separate and each gamete gets only one. In the F2 generation you see a 3:1 ratio!

F1 × F1: Aa × Aa → AA : 2Aa : aa
Phenotype: 3 dominant : 1 recessive

3️⃣ Law of Independent Assortment

The alleles of different genes (the ones sitting on different chromosomes) are inherited independently of each other.

Dihybrid cross: AaBb × AaBb → Ratio 9:3:3:1
📚 Key Definitions

Gene: A piece of DNA that codes for a trait
Allele: A different version of the same gene
Dominant (A): Always shows up when it is there
Recessive (a): Shows up only in the homozygous state
Homozygous: AA or aa (same alleles)
Heterozygous: Aa (different alleles)
Genotype: The alleles it has (AA, Aa, aa)
Phenotype: What we see (the trait)

📊 Punnett Square

A tool for predicting the offspring of a cross:

A a
A AA Aa
a Aa aa

Result: 25% AA, 50% Aa, 25% aa → Phenotype 3:1

🧬 Examples in Humans

The classic school examples, in their simplified form:

  • Eye color: Brown is dominant over blue
  • Earlobe: Free is dominant over attached
  • Tongue: Being able to "roll" it is dominant
  • Freckles: Presence is dominant over absence
⚠️ The truth is more complicated

These examples are handy for learning Mendel's laws, but in reality they are not controlled by just one gene:

Eye color is polygenic — more than 10 genes are involved. That's why green, gray and hazel eyes exist, and why two parents with blue eyes can have a child with brown eyes.
• The earlobe doesn't split neatly into "free" and "attached" — there is a continuous range.
Tongue rolling has been debunked: studies on identical twins (with identical DNA) found pairs where one can do it and the other can't.

Keep them as practice models, not as a description of reality.

⚠️ Exceptions to the Laws

Mendel's laws don't always hold! There are:

Incomplete dominance: The heterozygote has an in-between phenotype
Codominance: Both alleles are expressed (e.g. blood type AB)
Linked genes: Genes on the same chromosome are inherited together
Sex-linked inheritance: Genes on the sex chromosomes

📝 Worked Examples

📌 Example 1: Pea Seed Color

Yellow color (Y) is dominant over green (y).

Cross: Homozygous yellow (YY) × Homozygous green (yy)

Punnett square:

Y Y
y Yy Yy
y Yy Yy
F1 result: 100% Yy → All yellow (heterozygous)
This is the 1st Law — Uniformity!

📌 Example 2: F1 × F1 Cross

Continuing from example 1: we cross two heterozygous yellow plants (Yy).

Cross: Yy × Yy

Punnett square:

Y y
Y YY Yy
y Yy yy
F2 result:
• Genotype: 25% YY, 50% Yy, 25% yy (ratio 1:2:1)
• Phenotype: 75% yellow, 25% green (ratio 3:1)
This is the 2nd Law — Segregation!

📌 Example 3: Plant Height

Tall (T) is dominant over short (t).

Cross: Heterozygous tall (Tt) × Homozygous short (tt)

Punnett square:

T t
t Tt tt
t Tt tt
Result: 50% Tt (tall), 50% tt (short)
Phenotype ratio: 1:1 (a test cross!)

📌 Example 4: Eye Color in Humans

Brown color (B) is dominant over blue (b).

Question: A man with brown eyes (Bb) marries a woman with blue eyes (bb). What eye color will their children have?

Punnett square:

B b
b Bb bb
b Bb bb
Result: 50% brown eyes (Bb), 50% blue eyes (bb)

⚠️ Simplified model. In reality, eye color is decided by many genes, so the real ratios don't come out this neat.

📌 Example 5: Blood Types (Codominance)

Blood types are decided by 3 alleles: IA, IB, i

IA and IB are codominant with each other, but both are dominant over i.

Question: Father with type A (IAi) × Mother with type B (IBi)

Punnett square:

IA i
IB IAIB IBi
i IAi ii
Result:
• 25% AB (IAIB)
• 25% A (IAi)
• 25% B (IBi)
• 25% O (ii)
The children could have any of the 4 blood types!

📌 Example 6: Dihybrid Cross (3rd Law)

We look at 2 traits at the same time in pea plants:

• Color: Yellow (Y) is dominant over green (y)

• Shape: Round (R) is dominant over wrinkled (r)

Cross: YyRr × YyRr (dihybrids)

Gametes from each parent: YR, Yr, yR, yr

4×4 Punnett square:

YR Yr yR yr
YR YYRR YYRr YyRR YyRr
Yr YYRr YYrr YyRr Yyrr
yR YyRR YyRr yyRR yyRr
yr YyRr Yyrr yyRr yyrr
Phenotype ratio 9:3:3:1:
9 Yellow-Round
3 Yellow-Wrinkled
3 Green-Round
1 Green-Wrinkled

📌 Example 7: Incomplete Dominance — Flower Color

In Mirabilis jalapa flowers (the four o'clock flower), neither allele is fully dominant!

RR = Red

Rr = Pink (in between!)

rr = White

Cross: Pink (Rr) × Pink (Rr)

Punnett square:

R r
R RR Rr
r Rr rr
Result: 25% red, 50% pink, 25% white
A 1:2:1 ratio — genotype = phenotype!

📌 Example 8: Sex-Linked Inheritance — Color Blindness

Color blindness (daltonism) is a recessive trait carried on the X chromosome.

• XN = Normal vision

• Xn = Color blindness

Females: XNXN (normal), XNXn (carrier), XnXn (color blind)
Males: XNY (normal), XnY (color blind)

Cross: Carrier female (XNXn) × Normal male (XNY)

Punnett square:

XN Y
XN XNXN XNY
Xn XNXn XnY
Result:
25% Girl with normal vision (XNXN)
25% Carrier girl (XNXn)
25% Boy with normal vision (XNY)
25% Boy with color blindness (XnY)
Boys have a 50% chance of being color blind!

🎯 Practice Exercises

✏️ Exercise 1: Coat Color in Rabbits

Black (B) is dominant over brown (b).

Question: If we cross two heterozygous black rabbits (Bb × Bb), what color will the babies be?

👁️ See the answer
Answer: 75% black (BB or Bb), 25% brown (bb)
Ratio: 3:1

✏️ Exercise 2: Earlobes

The free earlobe (F) is dominant over the attached one (f).

Question: A man with free earlobes (Ff) marries a woman with attached earlobes (ff). What is the chance that their child has attached earlobes?

👁️ See the answer
Answer: 50% (or 1/2)
Offspring: 50% Ff (free), 50% ff (attached)

✏️ Exercise 3: Blood Type

Question: A mother has blood type O (ii) and the father has type AB (IAIB). Which blood types can their children have?

👁️ See the answer
Answer: 50% type A (IAi), 50% type B (IBi)
No child can be type O or type AB!

✏️ Exercise 4: Dihybrid Cross

In guinea pigs: Black (B) > white (b), Short hair (S) > long (s)

Question: Two dihybrids (BbSs × BbSs) are crossed. What is the chance of getting a white guinea pig with long hair?

👁️ See the answer
Answer: 1/16 (or 6.25%)
Ratio 9:3:3:1 — white with long hair (bbss) is the 1

🧬 How you inherit your DNA

Follow the steps and see how you get whole chromosomes from your mother and your father.

Step 1 / 23

🎯 Test Your Knowledge!

Answer the questions below to see how well you understood DNA!

1. Which base pairs with Adenine in DNA?

Guanine
Cytosine
Thymine
Uracil

2. How many chromosomes do humans have?

23
46
48
44

3. Which enzyme copies DNA?

Helicase
DNA Polymerase
Ligase
Primase

4. What is an SNP?

A type of RNA
A change in a single nucleotide
A chromosome
An enzyme

5. Who proposed the model of the double helix in 1953?

Mendel & Darwin
Avery & Griffith
Watson & Crick
Miescher & Chargaff

6. How many hydrogen bonds does the G-C pair have?

1
2
3
4

7. What percentage of DNA codes for proteins?

~1.5%
~25%
~50%
~90%

8. Where is DNA found inside the cell?

In the ribosomes
In the nucleus
Only in the mitochondria
In the cytoplasm

9. What is the ratio of phenotypes in Mendel's F2 generation?

1:1
2:1
3:1
4:1

10. What is a "heterozygous" individual?

It has two identical alleles (AA)
It has two different alleles (Aa)
It has no alleles
It has only one allele

11. Which organelle produces energy (ATP)?

Nucleus
Ribosomes
Mitochondria
Golgi apparatus

12. Who discovered the laws of inheritance?

Darwin
Mendel
Watson
Crick

13. What is the correct order: DNA → ... → Protein?

RNA
ATP
Amino acid
Chromosome

14. About how many genes do humans have?

~1,000
~20,000
~100,000
~1,000,000

15. Which mutation creates a premature stop codon and a shortened protein?

Silent
Nonsense
Missense
Frameshift

16. Why doesn't a silent mutation change the protein?

Because DNA fixes it right away
Because the genetic code is redundant — many codons give the same amino acid
Because it happens in non-coding DNA
Because it only changes the RNA

17. Which base is found in RNA but not in DNA?

Thymine (T)
Uracil (U)
Guanine (G)
Adenine (A)

18. How many chromosomes does a human egg cell have?

46
23
22
44

19. Which gamete decides whether the child will be XX or XY?

The egg cell, because it carries X or Y
The sperm cell, because it carries X or Y
Both equally
Neither — it is decided after fertilization

20. What does the karyotype of a person with trisomy 21 (Down syndrome) show?

45 chromosomes
47 chromosomes
46 chromosomes
48 chromosomes