gene
heritable factors that influence specific characteristics via a length of DNA that codes for a polypeptide
allele
alternative forms of a gene
homologous pairs
cells that have two copies of every gene
gene mutation
is a change in the sequence of base pairs in a DNA molecule which may result in a new allele
substitution mutation
a mutation that occurs when a base in the DNA sequence is randomly swapped for a different base
sickle cell anemia
when the base gene thymine (T) is replaced by the base adenine (A) within the hemoglobin gene causing the distortion in the shape of red blood cells
genome
the total of all genetic information in an organism
plasmids
very small circular DNA molecules that usually only contain a few genes.
histones
the main positively charged globular proteins in eukaryotic chromosomes
haploid cells
contain one complete set of chromosomes, meaning they have half the number of chromosomes compared to normal body cells
diploid cells
a pair of homologous chromosomes containing a full set
mitosis
gives rise to genetically identical cells and is the type of division used for growth, repair and replacement of cells
meiosis
gives rise to cells that are genetically different from each other and is used to produce gametes
meiosis I
the stage of meiosis when homologous pairs of chromosomes are split up, two produce two haploid (n) nuclei
meiosis II
The stage of meiosis when the chromatids that make up each chromosomes separate to produce four haploid (n) nuclei
gametes
the sex cells of an organism, which fuse during fertilization to form a zygote
dominant alleles
an allele which only needs to be inherited from one parent to be expressed
recessive alleles
an allele which needs to be inherited from both parents in order to expressed
gel electrophoresis
used to separate proteins or fragments of DNA according to size
cystic fibrosis
a genetic disorder of cell membranes caused by a recessive allele leading to the production of non-functional channels resulting in the body producing large amounts of mucus in the air passages
huntington’s disease
a genetic condition that develops as a person ages, with individuals experiencing neurological degeneration with it ultimately being fatal.
red-green color blindness
caused by a recessive allele found on the x chromosome responsible for the synthesis of of the photoreceptor proteins