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DNA
the molecule of heredity, passed from parents to offspring. stores biological information
chromosome
a single, large DNA molecule wrapped around proteins. located in the nuclei of eukaryotic cells. we have 23 pairs
XY
men
XX
women
what dna is made of
two strands of subunits (nucleotides) linked together in long chains
double helix
shape of DNA. spiral structure formed by two strands of DNA nucleotides held together by hydrogen bonds
dna replication
the natural process by which cells make an identical copy of a dna molecule, occurs when cells reproduce
complementary
fitting together, two strands of dna are said to be complementary. t and a. c ang g.
helicase
an enzyme that unwinds and unzips the dna double helix during dna replication
dna polymerase
an enzyme that reads the nucleotide sequence of a dna strand and incorporates complementary nucleotides into a new strand during replication. builds a new strang along each unzipped strand (helicase)
polymerase chain reaction (PCR)
laboratory technique to replicate a specific dna segment
James Watson and Francis Crick
solved the structure of dna
Rosalind Franklin
made xray diffraction pictures of dna
alleles
any of the alternative versions of the same gene that have different nucleotide sequences. created by mutations
diploid
having two copies of every chromosome
homologous chromosomes
a pair of chromosomes that both contain the same gene. one inherited from the mother, other from the father
phenotype
the visible or measurable features of an individual
genotype
the genetic makeup of an individual
gametes
specialized reproductive cells that carry one copy of each chromosome. sperm and eggs
haploid
having one copy of each chromosome. gametes for example
meiosis
a type of cell division that generate unique haploid gametes. happens in two events
zygote
a diploid cell that is able to develop into an adult organism. formed when a haploid egg is fertilized by a haploid sperm
mitosis
cell division that reproduces body cells
meiosis event 1 - recombination
maternal and paternal chromosomes pair and physically exchange dna segments
meiosis event 2 - independent assortment
alleles of different genes are distributed independently of one another during meiosis
heterozygous
having two different alleles for a given gene
homozygous
having identical alleles for a given gene
incomplete dominance
a form of inheritance in which heterozygotes have a phenotype that is intermediate between two homozygotes
codominance
a form of inheritance in which the effects of both alleles are displayed in the phenotype of a heterozygote
continuous variation
Variation in a population showing an unbroken range of phenotypes rather than discrete categories.
polygenic trait
a characteristic, such as height or skin color, that is influenced by two or more genes
multifactorial
An interaction between genes and the environment that contributes to a phenotype or trait.
epigenetics
Changes in gene expression that are not based on changes in the DNA sequence.