Chapter 2 Flashcards
(51 cards)
chromosome
one of 46 rodlike molecules that contain 23 pairs of DNA found in every body cell and collectively contain all of the genes
DNA
deoxyribonucleic acid; the chemical structure, shaped like a twisted ladder, that contains all of the genes
mitosis
the process of cell duplication in which DNA is replicated and the resulting cell is genetically identical to the original
meiosis
the process by which a gamete (sperm/ova) is formed, containing one-half of the cell’s chromosomes
zygote
a fertilized ovum
dizygotic twin
fraternal twin; occurs when two ova are released and each are fertilized by a different sperm; the resulting offspring share 50% of their genetic material
monozygotic twin
identical twin; occurs when the zygote splits apart early in development; the resulting offspring share 100% of their genetic material
homozygous
refers to a chromosomal pair consisting of two identical alleles
heterozygous
refers to a chromosomal pair consisting of two different alleles
dominant-recessive inheritance
a form of genetic inheritance in which the phenotype reflects only the dominant allele of a heterozygous pair
incomplete dominance
a genetic inheritance pattern in which both genes are expressed in the phenotype
sickle cell trait
a recessive trait, more often affecting African Americans that Caucasians or Asian Americans, that causes red blood cells to become crescent or sickle shaped, resulting in difficulty distributing oxygen throughout the circulatory system
polygenic inheritance
occurs when a trait is a function of the interaction of many genes, such as with height, intelligence, and temperament
genomic imprinting
the instance when the expression of a gene is determined by whether it is inherited from the mother or father
phenylketonuria (PKU)
a recessive disorder that prevents the body from producing an enzyme that breaks down phenylalanine (an amino acid) from proteins, that, without treatment, leads to buildup that damages the central nervous system
fragile X syndrome
an example of a dominant-recessive disorder carried on the X chromosome
down syndrome
also known as trisomy 21; a condition in which a third, extra chromosome appears at the 21st site; down syndrome is associated with distinctive physical characteristics accompanied by developmental disability
mutation
a sudden permanent change in the structure of genes
genotype
an individual’s collection of genes that contain instructions for all physical and psychological characteristics, including hair, eye color, personality, health, and behavior
phenotype
the observable physical or behavioral characteristics of a person
behavioral genetics
the field of study that examines how genes and environment combine to influence the diversity of human traits, abilities, and behaviors
heritability
a measure of the extent to which variation of a certain trait can be traced to genes
gene-environment interactions
refers to the dynamic interplay between our genes and our environment in determining our characteristics, behavior, physical, cognitive, and social development as well as health
range of reaction
the concept that a genetic trait may be expressed in a wide range of phenotypes dependent on environmental opportunities and constraints