synthesis phase of the cell cycle
stage of interphase were DNA replicates
cell's nucleus divides occurs in 5 stages
Prophase, Metaphase, Anaphase, Telophase
results in 2 daughter cells same number of chromosomes as parent cell
genetic copies of each other ( identical) made during S-phase of interphase
held together by a centromere
pairs of chromosomes that carry the same genes
made of 4 chromatids (tetrad)
`a homologous pair formed during prophase of meiosis
four chromatids
chromatin thickens to form X shaped chromosomes
each half of X is a copy of original chromosome (chromatid) held together by a centromere
nucleus disappears, centrioles move to poles, spindle fibers form
everything moves to the middle
spindle fibers attach to centromeres of chromatids
centromeres split apart
chromatids are split and are pulled to opposite poles of cell
nuclear membrane reappears
cytoplasm is pinched
two daughter cells begin to form
chromatid is now chromatin
division of cells
separation of cytoplasm
spindle fibers disappear
nucleus reappears
result is 2 daughter cells with same number of chromosomes as parent cell
haploid reproductive cells
either sperm or egg
produced during meiosis
developing embryo
hollow Ball of cells
a thin walled structure containing cluster of cells that an embryo comes from
every cell that just undergoes mitosis
body cell not reproductive cells ex: skin cells
fertilized ovum
diploid cell from 2 haploid cell
cells that carry half the number of chromosomes (n) as diploids
gametes, egg or sperm
process of sperm production
occurs in testes
starts with diploid cell: spermatogonium, which grows and then under goes meiosis I and Meiosis II
the result is 4 haploid sperm cells
form throughout adult years
process of egg production
occurs in ovaries
starts with diploid cell: oogonium, which grows and undergoes meiosis I and meiosis II, the cytoplasm doesn't equally divide in meiosis
the result is 3 polar bodies and 1 egg cell
error in number
homologue pairs don't separate properly or sister chromatids don't separate properly
error in structure
when a segment of DNA is flipped and attaches at the wrong end
error in structure
when a segment of DNA is deleted
error in structure
when a segment of DNA breaks off and rejoins in a different spot
error in structure
a section of a chromosome appears 2+ times in a row
Prenatal genetic testing
14 weeks of pregnancy
amniotic fluid is taken from amniotic sac and fetal cells are tested to see if there are any genetic abnormalities (Trisomy 21)
Prenatal genetic testing
9 weeks of pregnancy
chorion fetal cell sample is taken
In Vitro Fertilization (external)
eggs and semen are collected
fertilization occurs in a lab "Test tube babies"
embryo transfer (external)
egg is fertilized outside and implanting it into females uterus
Deoxyribonucleic Acid
found in nucleus
control production of proteins in the cell
double helix shape
never leaves nucleus
Adenine pair w/ Thymine, Cytosine pair w/ Guanine
Uracil (RNA)
DNA copies itself
semi-conservative: ea. new piece of DNA is made of 1 original strand and 1 new strand
DNA unzips, original strand grows new strand
copy of DNA that leaves nucleus
ribonucleic acid
U, A, C, G
unzip one gene in DNA
match up bases to 1 side of a gene in DNA
mRNA detaches and moves out and into cytoplasm
message that codes for protein
moves out of nucleus and into cytoplasm
process of making a protein
mRNA > cytoplasm > attaches to ribosome > tRNA decodes mRNA and bring amino acids to build protein
20 different kinds
building blocks of proteins
genetic make-up of an organism
the 2 alleles inherited from your parents ex: Dd is a genotype for dimples
the expression of the genotype
appearance of a trait in an individual ex: DD= dimples dd= no dimples
organisms from a distinct type or breed (tall w/ tall and short w/ short)
share similar traits
organism heterozygous for a trait
hybrid cross between 2 different purebred plants (tall w/ short)
trait that is not usually expressed but is still there
if its homozygous recessive it will be expressed
blending of two traits
neither alleles are dominant and a blend of the traits show (red and white genotypes express pink phenotypes)
individual who has an unhealthy/recessive allele on 1 part of the chromosome but doesn't express it
can pass it on to offspring
traits are determined by pairs of alleles from each parent
offspring get one allele from each parent
gene that is found on the X chromosome
mothers may be carriers and don't express the trait