Mendel and the Gene Idea: Chp 14 Flashcards
p generation
true-breeding parents in a genetic cross
f1 generation
p generation offspring
f2 generation
f1 generation offspring
four concepts explaining mendel’s 3:1 inheritance pattern
1: alternative versions of genes cause variations in inherited characteristics among offspring
2: for each character, every organism inherits one allele from each parent
3: if the two alleles are different, then the dominant allele will be fully expressed
4: the two alleles for each character separate during gamete production
mendels law of segragation
states that allele pairs separate or segregate during gamete formation, and randomly unite at fertilization
mendels law of independent assortment
states that each pair of alleles will segregate independently during gamete formation
homozygous
two of the same alleles
heterozygous
two different alleles
phenotype
refers to an organisms expressed physical traits
genotype
refers to an organisms genetic makeup
testcross
is done to determine if an individual showing a dominant trait is homozygous or heterozygous
monohybrid cross
a cross involving the study of only one character
dihybrid cross
a cross intended to study two characters
the rule of multiplication
when calculating the probability that two or more independent events will occur together in a specific combination, multiply the probabilities of each of the two events
the rule of addition
when calculating the probability that any of two or more mutually exclusive events will occur, you need to addd together their individual probabilities
complete dominance
dominance in which the heterozygote and the homozygote for the dominant allele are indistinguishable
co dominance
occurs when two alleles are dominant and affect the phenotype in two different but equal ways
incomplete dominance
a type of dominance in which the F1 hybrids have an appearance that is in between that of the two parents
multiple alleles
occur when a gene has more than two alleles
pleiotrophy
the property of a gene that causes it to have multiple phenotypic effects
epistasis
a gene at one locus alters the effects of a gene at another locus
polygenic inheritance
two or more genes have an additive effect on a single character in the phenotype
pedigree
a diagram that shows the relationship between parents and offspring across two or more generations. Circles represent females and squares represent males.
recessively inherited disorders
require two copies of the defective gene for the disorder to be expressed
cystic fibrosis
caused by a mutation in an allele that codes for a cell membrane protein that functions in the transport of chloride ions into and out of the cells. the resulting high extracellular levels of chloride cause mucus to be thicker and stickier, leading to organ malfunction and recurrent bacterial infections
tay-sachs disease
is caused by an allele that codes for a dysfuntional enzyme, which is unable to break down certain lipids in the brain. as they accumulate in the brain cells, the child suffers from blindness, seizures, and degeneration of brain function, leading to death
sickle cell disease
caused by an allele that codes for a mutant hemoglobin molecule that forms long rods when the oxygen levels in the blood are low these long rods cause the red blood cell to sickle, clogging small blood vessels and leading to pain, organ damage, and even paralysis
lethal dominant alleles
require only one copy of the allele in order for the disorder to be expressed. usually, only late-acting lethal alleles are passed on
huntingtons disease
caused by a lethal dominant allele. it is a degenerative disease of the nervous system, which usually doesn’t affect the individual until he or she is over 40years old
amniocentesis
occurs when the physician removes amniotic fluid from around the fetus. the amniotic fluid can be utilized to detect some genetic disorders, and the cells in the fluid can be cultured for a karyotype
chorionic villus sampling
involves using a narrow tube inserted through the cervix to suction out a tiny sample of the placenta that contains only fetal cells. a karyotyp can immediately be developed from these cells