Genetics Test
GENETICS STUDY GUIDE
I. Genetics Basics
Definition: Study of how genes/traits are passed down generations.
II. DNA (Deoxyribonucleic Acid)
Structure:
Double-stranded, double helix, found in nucleus, makes up chromosomes.
Genes: Portions of DNA coding for traits.
Nucleotide Parts:
Nitrogenous bases:
Adenine (A) ↔ Thymine (T)
Cytosine (C) ↔ Guanine (G)
Sugar: Deoxyribose
Phosphate group
Replication:
Exact duplication before cell division.
Enzymes: Helicase (unzips), DNA Polymerase (adds nucleotides).
III. RNA (Ribonucleic Acid)
Structure: Single-stranded.
Types:
mRNA: Carries DNA message to ribosome.
tRNA: Brings amino acids to ribosome.
rRNA: Makes ribosomes.
Nitrogenous bases:
Adenine (A) ↔ Uracil (U)
Cytosine (C) ↔ Guanine (G)
IV. Processes
Transcription: DNA → mRNA (Uracil replaces Thymine).
Enzyme: RNA Polymerase.
Example:
DNA: T-A-G-C
mRNA: A-U-C-G
Translation:
Ribosome reads mRNA.
tRNA brings amino acids.
Codons (3 nucleotides) → Amino acids.
Example:
DNA: T-A-G
mRNA: A-U-C
Amino acid: Iso
VI. Mutations
Types:
Gene Mutations:
Deletion: Nucleotide missing.
Insertion: Nucleotide added.
Inversion: Segment reattaches incorrectly.
Translocation: Segment attaches to different chromosome.
Chromosomal Mutation: Change in chromosome number (e.g., Trisomy 21 - Down Syndrome).
VII. Mendelian Genetics
Key Terms:
Phenotype: Physical traits.
Genotype: Genetic makeup (AA, Aa, aa).
Alleles: One from each parent.
Dominant allele always expressed if present.
Punnett Square: Predicts genotype/phenotype probabilities.
Good luck on your test! 🚀