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A complete question and answer flashcard set covering foundational genetics definitions from DNA structure and inheritance to population genetics and evolutionary mechanisms.
DNA
A long strand of genetic information that contains the code for all aspects of your body.
shape of DNA
Double Helix.
nucleotides
The monomers that make up DNA, which contain phosphate, sugar, and a base.
weak bonds between bases
Hydrogen Bonds.
complementary base pairing
A bonds with T, G bonds with C.
chromosome
Packaged DNA containing many genes.
genetic code
The order of the bases.
gene
A section of DNA that codes for a particular trait.
46 Chromosomes.
the number of chromosomes in human body cells
Organelle that contains DNA in a cell
Nucleus.
asexual reproduction
Offspring from one parent which is genetically identical.
meiosis
Cell division to make gametes with half the chromosome number.
site of meiosis in animals
Ovary, testes.
number of chromosomes in human gametes
23 Chromosomes.
independent assortment
Homologous pairs of chromosomes line up in random order on the equator during first division of meiosis giving new allele combinations.
crossing over
Sections of homologous chromosomes swap before the 1st division of meiosis giving new allele combinations.
variation
Differences between individuals.
genetic variation
Differences in the DNA/alleles between individuals.
sexual reproduction
Offspring formed from the fusing of gametes mixing the genetics of 2 parents.
homologous chromosomes
Pair of chromosomes with the same genes on them in the same place.
zygote
Fertilized egg with whole set of chromosomes.
homozygous
Both alleles are the same (eg BB, bb).
heterozygous
Two alleles are different (eg Bb).
dominant allele
Only one allele is required for this phenotype to be expressed.
recessive alleled
Both alleles are required for this phenotype to be expressed.
phenotype
Physical expression of the gene.
genotype
Combination of alleles present for a gene.
pure breeding
Homozygous, the offspring will always show the dominant trait.
mutation
Permanent change in base sequence of DNA (makes new alleles).
pedigree chart
Family tree showing phenotypes of individuals in a family over generation.
carrier
Heterozygous/has one dominant and one recessive allele for a disease.
gene pool
Total number of all the alleles in a population.
allele frequency
The number/proportion of one type of allele in a gene pool.
genetic drift
Random change in allele frequency by chance, lowering genetic variation.
bottleneck effect
A catastrophic event results in only a small population surviving.
founder effect?
A small number of an original population relocate to a new area forming a new, small population.
gametic mutation
Mutation that occurs in a gamete and can be passed on to offspring.
somatic mutation
Mutation that occurs in a 'body' (somatic) cell so cannot be passed on.
migration
Gene flow/Individuals move into or out of the population.
immigration
Individuals move INTO a population, increasing genetic variation.
emigration
Individuals EXIT from a population, decreasing genetic variation.
natural selection
Individuals with alleles that give them a phenotype that gives them a survival and reproductive advantage will pass on these 'fit' alleles more often, so increase in frequency in the gene pool.
gene tracking
Following the inheritance of a specific gene.
DNA sequencing
Determining the base order of DNA.
genetic marker
A section of DNA that is unique to an individual or family.
relatedness
How closely related living things are (eg same family/ancestry).
diagnosis
DNA sequencing and tracking to see if an individual has an allele/mutation.
genetic variation important
Some members of the population might have alleles that give them resistance to a disease/environmental change so they survive and reproduce.
inbreeding
When two closely related individuals breed.
captive breeding
Selecting individuals from an endangered population and placing them in a safe environment (no predators, lots of food/resources) to reproduce.