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A set of vocabulary-style flashcards covering heredity, genetic code, cell division, mutation, genetic crosses, and blood type/paternity concepts.
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Heredity
Transmission of traits from parents to offspring.
Genetics
The study of heredity and variation.
Genes
Segments of DNA that code for traits (e.g., eye colour, blood type).
Alleles
Alternative forms of a gene (e.g., A and a).
Genotype
Genetic makeup; the combination of alleles (e.g., AA, Aa, aa).
Phenotype
Physical appearance or trait (e.g., brown eyes).
Dominant
An allele that shows in the phenotype if at least one copy is present.
Recessive
An allele that shows in the phenotype only when two copies are present.
DNA
Deoxyribonucleic acid; the molecule that stores genetic information; double helix.
Double helix
The two intertwined strands that make up the DNA molecule.
Nucleotides
Building blocks of DNA: phosphate + deoxyribose sugar + nitrogen base.
Bases
A, T, G, C; pair via A–T and G–C.
Base-pairing rule
A pairs with T; G pairs with C.
Coding DNA
DNA regions that code for proteins; a gene is part of coding DNA.
RNA
Ribonucleic acid; single-stranded molecule made during transcription; bases A, U, G, C; U replaces T.
mRNA
Messenger RNA; carries code from DNA to the ribosome.
tRNA
Transfer RNA; brings amino acids to the ribosome.
rRNA
Ribosomal RNA; makes up ribosomes.
Codon
A group of three RNA bases that codes for one amino acid.
Codon table
Chart that translates mRNA codons into amino acids.
Start codon
AUG; codes for Methionine and signals the start of translation.
Methionine
Amino acid encoded by the start codon AUG.
Proline
Amino acid encoded by certain codons (e.g., CCU).
Lysine
Amino acid encoded by codons such as AAG.
Amino acids
Building blocks of proteins; amino acids are coded by codons.
Mitosis
Cell division for growth, repair, and asexual reproduction; results in 2 identical diploid cells.
Meiosis
Cell division for sexual reproduction; produces 4 non-identical haploid cells; increases genetic variation.
PMAT
Stages of mitosis: Prophase, Metaphase, Anaphase, Telophase.
Crossing over
Exchange of chromosome segments during meiosis; increases genetic variation.
Independent assortment
Random orientation of homologous chromosomes during meiosis; increases variation.
Mutation
A change in the DNA sequence.
Point mutation
One base changes.
Insertion
A base added to the DNA sequence.
Deletion
A base removed from the DNA sequence.
Frameshift
Insertion or deletion that shifts the reading frame of a gene.
Spontaneous
Mutations caused by natural replication errors.
Induced
Mutations caused by radiation, chemicals, UV light.
Neutral
Mutation that has no effect on organism fitness.
Harmful
Mutation that negatively affects the organism (e.g., disease).
Beneficial
Mutation that provides a selective advantage (e.g., antibiotic resistance).
Genetic cross
Breeding experiment to study inheritance patterns.
Punnett square
Diagram used to predict offspring genotypes and phenotypes from parental genotypes.
Monohybrid cross
A cross involving one trait (e.g., height with dominant and recessive alleles).
Trait
A characteristic such as height or eye colour.
Dominant trait
Trait expressed when at least one dominant allele is present (e.g., tall).
Recessive trait
Trait expressed only when two recessive alleles are present (e.g., short).
ABO system
Blood group system controlled by one gene with three alleles: A, B, O.
Genotypes (ABO)
A = AA or AO; B = BB or BO; AB = AB; O = OO.
Codominant
A and B alleles are codominant; O is recessive.
Paternity testing
Process used to exclude possible fathers before DNA testing.
Exclude
Rule out a potential father based on evidence (e.g., blood type incompatibility).