Chapter 2 Flashcards
Genotype
An individuals unique genetic information
Phenotype
An individual’s directly observable characteristics
Chromosomes
Structures that store and transmit genetic information
DNA
Chemical substance of which chromosomes are made
Gene
Segment of DNA along the length of a chromosome
Protein-coding genes
Directly affect the body’s characteristics
Regulator genes
Modify instructions given by protein-coding genes
Meiosis
Cell devision process that halves the number of chromosomes normally present in body cells; shuffling of genes produces genetic variability (which is adaptive)
Gametes
Sex cells (sperm and ovum) created by meiosis
Zygote
Cell formed when sperm and ovum unite at conception; contains 46 chromosomes
Autosomes
22 matching pairs of chromosomes
Sex chromosomes
Twenty-third pair of chromosomes; XX in females, XY in males (X chromosome is relatively long, Y is short and carries little genetic material)
Fraternal (dizygotic) twins
Results from fertilization of two ova; no more alike than ordinary siblings
Identical (monozygotic) twins
Results from separation of a single zygote into two clusters of cells; have the same genetic makeup
Alleles
Two forms of a gene, one inherited from each parent; occur at same place on both chromosomes in a pair
Homozygous
Alleles from both parents are alike
Heterozygous
Alleles differ
Dominant-recessive inheritance
Only the dominant allele affects child’s characteristics; heterozygous individuals can be carries, homozygous inheritance of recessive alleles can cause serious disabilities and diseases
Example: PKU
Incomplete-dominance pattern
Both alleles expressed in phenotype; results in combined trait (or intermediate between the two)
Example: sickle cell trait
X-linked pattern
Harmful allele carried on X chromosome (males are more likely to be affected)
Examples: hemophilia, fragile X syndrome