50 terms

BIOL 102 Chp 14: Mendel and the Gene Idea

This flashcard set includes the vocabulary words and definitions from Chp 14: Mendel and the Gene Idea (Biology 9E by Campbell et al, 2011). http://robswatski.virb.com
an observable heritable feature
any detectable variant in a genetic character
true breeding
referring to plants that produce offspring of the same variety when they self-pollinate
the mating, or crossing, of two true-breeding varieties
P generation
the parent individuals from which offspring are derived in studies of inheritance
F1 generation
the first filial, or hybrid, offspring in a series of genetic crosses
F2 generation
offspring resulting from interbreeding of the hybrid F1 generation
any of the alternative versions of a gene that produce distinguishable phenotypic traits
dominant allele
a gene that is fully expressed in the phenotype of a heterozygote
recessive allele
a gene whose phenotypic effect is not observed in a heterozygote
law of segregation
states that the two alleles in a pair separate into different gametes during gamete formation
Punnett square
a diagram used in the study of inheritance to show the predicted results of random fertilization in genetic crosses
having two identical alleles for a given gene
having two different alleles for a given gene
the physical and physiological traits of an organism, which are determined by its genetic makeup
the genetic makeup, or set of alleles, of an organism
breeding an organism of unknown genotype with a homozygous recessive individual to determine the unknown genotype
an organism that is heterozygous with respect to a single gene of interest
an organism that is heterozygous with respect to two genes of interest
law of independent assortment
states that each pair of alleles separates independently of other pairs during gamete formation; applies when genes for two characters are located on different pairs of homologous chromsomes
complete dominance
the situation in which the phenotypes of the heterozygote and dominant homozygote are indistinguishable
incomplete dominance
the situation in which the phenotype of heterozygotes is intermediate between the phenotypes of individuals homozygous for either allele
the situation in which the phenotypes of both alleles are exhibited in the heterozygote because both alleles affect the phenotype in separate, distinguishable ways
Tay Sachs disease
a human genetic disease caused by a recessive allele for a dysfunctional enzyme, leading to accumulation of certain lipids in the brain; results in seizures, blindness, and degeneration of motor and mental performance a few months after birth, followed by death within a few years
the ability of a single gene to have multiple effects; Ex: the multiple symptoms associated with certain hereditary diseases such as cystic fibrosis and sickle-cell disease
a type of gene interaction in which one gene alters the phenotypic effects of another gene that is independently inherited
quantitative character
a heritable feature that varies continuously over a range rather than in an either-or fashion
polygenic inheritance
an additive effect of two or more genes on a single phenotypic character; Ex: skin pigmentation in humans
norm of reaction
the range of phenotypes produced by a single genotype, due to environmental influences
refers to a phenotypic character that is influenced by multiple genes and environmental factors
a diagram of a family tree showing the occurrence of heritable characters in parents and offspring over multiple generations
an individual who is heterozygous at a given genetic locus, with one normal allele and one recessive allele, who can pass on the recessive allele to offspring
cystic fibrosis
a human genetic disorder caused by a recessive allele for a chloride channel protein; characterized by an excessive secretion of mucus and consequent vulnerability to infection; fatal if untreated
sickle cell disease
a human genetic disease caused by a recessive allele, resulting in the substitution of a single amino acid in a globin polypeptide that is part of the hemoglobin protein; characterized by deformed red blood cells that can lead to numerous symptoms
Huntington's disease
a human genetic disease caused by a dominant allele, characterized by uncontrollable body movements and degeneration of the nervous system; usually fatal 10 to 20 years after the onset of symptoms
a technique of prenatal diagnosis in which amniotic fluid, obtained by aspiration from a needle inserted into the uterus, is analyzed to detect certain genetic and congenital defects in the fetus
chorionic villus sampling
a technique of prenatal diagnosis in which a small sample of the fetal portion of the placenta is removed and analyzed to detect certain genetic and congenital defects in the fetus
blending hypothesis
the idea that genetic material contributed "mix" together in a way that blue + yellow make green; predicts that over many generations a freely mating population would give rise to a uniform population of individuals; fails to explain how some traits reappear after skipping a generation; disproved by Gregor Mendel
the pollen-producing organ of a flower
the egg-bearing organ of a flower
cross pollination
fertilization between different plants
a specific place along the length of a chromosome where a given gene is located
monohybrid cross
a cross between individuals that involves one pair of contrasting traits
dihybrid cross
a cross between individuals concentrating on two definable traits
multiplication rule
a rule of probability stating that the probability of two or more independent events occurring together can be determined by multiplying their individual probabilities
addition rule
the probability that any one of two or more mutually exclusive events will occur is calculated by adding together their individual probabilities
multiple alleles
three or more forms of a gene that code for a single trait; Ex: ABO blood group in humans
a form of human dwarfism caused by a single dominant allele; the homozygous condition is lethal
an autosomal recessive hereditary condition characterized by a partial or total lack of melanin pigment, particularly in the eyes, skin, and hair
newborn screening
the analysis of a neonate's blood for metabolic or genetic disorders to prevent mental retardation, disability or death