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DNA
A complex molecule containing the genetic information that makes up the chromosomes.
RNA
single-stranded nucleic acid that contains the sugar ribose
nucleus
Control center of the cell
nuclear pores
small holes in the nuclear envelope where the RNA leaves from
cytoplasm
the material or protoplasm within a living cell, excluding the nucleus.
ribosome
Makes proteins; RNA travels here after being in nucleus
rough ER
proteins are modified here before they are packaged into vesicle and sent into the cytoplasm
vesicle
Small membrane-bound sac that functions in moving products into, out of, and within a cell.
golgi body
where proteins are completed
cell membrane
A cell structure that controls which substances can enter or leave the cell.
protein
A three dimensional polymer made of monomers of amino acids.
mitosis
1->2 new cells, creates identical cells, new cells have identical fulls sets of DNA
meiosis
1->4 cells, 4 genetically unique cells, creates gametes that combine to create new individuals, 1/2 of the og DNA
gametes
sex cells
punnet squares
used to predict the outcome of sexual reproduction
genotype
genetic makeup(DNA)
pheotype
visible traits
transcription
DNA to RNA
translation
RNA to protein
DNA synthesis
DNA to new DNA (copies DNA)
nucleotides
monomers of nucleic acids
nucleic acids
DNA and RNA
amino acids
monomers of proteins
monomer
building block
polymer
finished product
adenine
The base that pairs with Thymine in DNA, and Uracil in RNA
thymine
The base that pairs with Adenine in DNA
guanine
The base that pairs with Cytosine
cytosine
The base that pairs with Guanine
uracil
Nitrogen base that pairs with adenine in RNA.
codon table
shows all possible codons & the amino acid each codes for
mRNA
messenger RNA; instructions to make a protein
rRNA
ribosomal RNA; goes out into cytoplasm & it coils up in a Z part shape to make a ribosome
tRNA
transfer RNA; finds the correct amino acids & brings it to ribosome
chromatin
Substance found in eukaryotic chromosomes that consists of DNA tightly coiled around histones
genes
sections of DNA that code for a unique protein
chromosome
loose coiled DNA that are actively being used
centromere
Area where the chromatids of a chromosome are attached
sister chromatids
original chromosome duplicated & the two are attached at centromere
homologous chromosomes
Pair of chromosomes that are the same size, same appearance and same genes.
Heterozygous chromosomes
Chromosomes that have a different sequence of genes and a different structure.
prophase
first phase, chromosomes are visible & nucleus has dissolved
metaphase
chromosomes line up in middle of cell
anaphase
sister chromatids move to opposite sides of cell (apart)
telephase
DNA is now in two identical nuclei but still in one cell
spindle
equator of cell (middle)
cytokenesis
physical division of the cytoplasm, membrane & organelles into two new cells
PMAT I
Prophase I, metaphase I, anaphase I, telophase I- first stage of meiosis
PMAT II
Prophase II, metaphase II, anaphase II, telophase II- first stage of meiosis, with two cells instead of one
crossing over
homologous chromosomes overlap & swap
karyotype
picture of chromosomes-arranged from largest->smallest
monosomy
missing a chromosome
trisomy
having an extra chromosome
amniocentisis
prenatal diagnosis in which amniotic fluid, taken from a needle inserted into the uterus, is analyzed to detect certain genetic and congenital defects in the fetus.
diploid
full set of DNA (from both parents combined)
haploid
half of the DNA (only from 1 of 2 parents)
somatic cell
any cell of a living organism other than the reproductive cells.
frame shift mutation
a nucleotide is added or deleted, which changes the entire protein sequence
substitutions
point mutations that replace one nucleotide with another; can be harmful or harmless
silent mutations
harmless mutations
alleles
versions of the same gene
simple dominance
cross of two genes in which one is dominant over recessive
co-dominance
both alleles for a gene are expressed
multiple alleles
an allele of a genetic locus having more than two allelic forms within a population
incomplete dominance
one allele is not dominant over another, they combine
environmental influence
gene influenced by environmental factor
polygenic inheritance
multiple genes determine the phenotype of a trait
sex-linked traits
traits controlled by gene located on sex chromosomes
sexual selection
extreme traits in males of a species used to attract mates or compete for mating opportunities. traits can have drawbacks, but lead to better chance of reproudction
artificial selection
humans select traits in organisms
stabilizing selection
the average trait is the most useful
directional selection
extreme traits are favored
speciation
the formation of new species