Genetics and Evolution Flashcards
contain genes in a linear sequence
chromosomes
alternative forms of a gene
alleles
the combination of alleles one has at a given genetic locus
genotype
occurs when the effect of one allele completely masks the effect of another
complete dominance
occurs when there is more than one dominant allele
codominance
occurs when there are no dominant alleles; heterozygotes have intermediate phenotypes
incomplete dominance
the proportion of a population with a given genotype who express the phenotype
penetrance
refers to the varying phenotypic manifestations of a given genotype
expressivity
states that an organism has two alleles for each gene, which segregate during meiosis, resulting in gametes carrying only one allele for a trait
Mendel’s first law (of segregation)
states that inheritance of one allele does not influence the probability of inheriting an allele for a different trait
Mendel’s second law (of independent assortment)
support for DNA as genetic material:
demonstrated the transforming principle, converting nonvirulent live bacteria into virulent bacteria by exposure to heat-killed virulent bacteria
Griffith experiment
support for DNA as genetic material:
demonstrated that DNA is the genetic material because degradation of DNA led to a cessation of bacterial transformation
Avery-MacLeod-McCarty experiment
support for DNA as genetic material:
confirmed that DNA is the genetic material because only radio-labeled DNA could be found in bacteriophage-infected bacteria
Hershey-Chase experiment
includes all of the alleles in a given population
gene pool
changes in DNA sequence
mutations
include point mutations and frameshift mutations
nucleotide mutations
nucleotide mutations:
the substituting of one nucleotide for another
point mutations
nucleotide mutations:
moves the three-letter transcriptional reading frame
frameshift mutation
nucleotide mutations:
has no effect on the protein
silent mutation
nucleotide mutations:
results in the substitution of one amino acid for another
missense mutation
nucleotide mutations:
results in the substitution of a stop codon for an amino acid
nonsense mutation
nucleotide mutations:
result in a shift in the reading frame, leading to changes for all downstream amino acids
insertions and deletions (indels)