Interphase
Cell grows, copies its DNA, and synthesizes proteins, prepares for division
G1, S, and G2 phases,
G1 phase
stage of interphase in which cell grows
S phase
synthesis phase of the cell cycle
stage of interphase were DNA replicates
G2 phase
last stage of interphase where cell grows and prepares for mitosis
Mitosis (M phase)
cell's nucleus divides occurs in 5 stages
Prophase, Metaphase, Anaphase, Telophase
results in 2 daughter cells same number of chromosomes as parent cell
Chromosome
structures in a nucleus that contain cell's genetic information
Spindle fibre
tiny tube-like structures made of protein, chromosomes attach during cell division
Centriole
cylindrical organelle in animal cells aiding in cell division
Sister Chromatids
genetic copies of each other ( identical) made during S-phase of interphase
held together by a centromere
Chromatin
uncoiled chromosomes in DNA before cell division occurs
Centromere
region where two sister chromatids are held together
Homologous chromosomes
pairs of chromosomes that carry the same genes
made of 4 chromatids (tetrad)
Tetrad
`a homologous pair formed during prophase of meiosis
four chromatids
Prophase
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
Metaphase
everything moves to the middle
spindle fibers attach to centromeres of chromatids
Anaphase
centromeres split apart
chromatids are split and are pulled to opposite poles of cell
Telophase
nuclear membrane reappears
cytoplasm is pinched
two daughter cells begin to form
chromatid is now chromatin
Cytokinesis
division of cells
separation of cytoplasm
spindle fibers disappear
nucleus reappears
result is 2 daughter cells with same number of chromosomes as parent cell
Meiosis
process of reproduction division where the # of chromosomes is divided in 2 (diploid to haploid)
Crossing over
exchange in alleles between homologous chromosomes, producing new allele combinations
Meiosis I
Interphase: G1, S, G2, chromatin replicates into chromatid Prophase I: centrioles move to poles, tetrad, crossing over Metaphase I: spindle fibres attach to homologous pairs, tetrads line up at equator Anaphase I: spindle fibers pull homolgous pairs to poles Telophase I: nuclear membranes form, cytoplasm pinches Cytokinesis: 2 new unique cells are formed, DNA from both mom and dad allele in new cells,
Meiosis II
Prophase II: centrioles move to poles, tetrad, crossing over Metaphase II: spindle fibres attach to homologous pairs, tetrads line up at equator Anaphase II: spindle fibers pull homolgous pairs to poles Telophase II: nuclear membranes form, cytoplasm pinches Cytokinesis: 2 new unique cells are formed
result is 4 unique cells with 1/4 DNA of parent cell (gamete)
Cell differentiation
when cells are assigned jobs
Gamete
haploid reproductive cells
either sperm or egg
produced during meiosis
Blastocysts
developing embryo
hollow Ball of cells
a thin walled structure containing cluster of cells that an embryo comes from
Somatic cell
every cell that just undergoes mitosis
body cell not reproductive cells ex: skin cells
Sex cell
egg or sperm; a sex cell carries half the number of chromosomes found in the other body cells.
Zygote
fertilized ovum
diploid cell from 2 haploid cell
Diploid
cells that carry two copies of every chromosome (2n)
Haploid
cells that carry half the number of chromosomes (n) as diploids
gametes, egg or sperm
Spermatogenesis
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
Oogenesis
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
Bivalent
-the structure formed by the pair of homologous chromosomes during crossing over. Also called a tetrad because it consists of four chromatids.
Sex chromosome
X or Y chromosome that carry the gene used to determine the sex of a person
Non-disjunction
error in number
homologue pairs don't separate properly or sister chromatids don't separate properly
Inversion
error in structure
when a segment of DNA is flipped and attaches at the wrong end
Deletion
error in structure
when a segment of DNA is deleted
Translocation
error in structure
when a segment of DNA breaks off and rejoins in a different spot
Duplication
error in structure
a section of a chromosome appears 2+ times in a row
Amnioscentesis
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)
CVS (chronic villus sampling)
Prenatal genetic testing
9 weeks of pregnancy
chorion fetal cell sample is taken
Selective breeding
process of breeding organisms for desirable traits
Artificial Insemination
artificial transfer of semen into female reproductive tract
IVF
In Vitro Fertilization (external)
eggs and semen are collected
fertilization occurs in a lab "Test tube babies"
ET
embryo transfer (external)
egg is fertilized outside and implanting it into females uterus
What is PGD?
Preimplantation Genetic Diagnosis
Ultrasound
sound waves are sent through the body to get an image of organs or fetus
James Watson and Francis Crick
determined structure of DNA
DNA
Deoxyribonucleic Acid
found in nucleus
control production of proteins in the cell
double helix shape
never leaves nucleus
Gene
segment of DNA on a chromosome that codes for a specific trait
Nitrogenous base
Adenine pair w/ Thymine, Cytosine pair w/ Guanine
Uracil (RNA)
Nucleotide
repeating unit of sugar (deoxyribose), phosphate and 1 base
Hydrogen bond
what holds the sides of DNA ladder together
Codon
specific sequence of 3 adjacent bases on a strand of DNA or RNA that provides genetic code information for a particular amino acid
DNA replication
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
RNA
copy of DNA that leaves nucleus
ribonucleic acid
U, A, C, G
Transcription
unzip one gene in DNA
match up bases to 1 side of a gene in DNA
mRNA detaches and moves out and into cytoplasm
mRNA
message that codes for protein
moves out of nucleus and into cytoplasm
Translation
process of making a protein
mRNA > cytoplasm > attaches to ribosome > tRNA decodes mRNA and bring amino acids to build protein
Amino acid
20 different kinds
building blocks of proteins
Mutation
error in DNA sequence
Mutagen
anything that causes change in DNA ex: x-rays, UV light, nuclear radiation
Trisomy 21
condition in which an individual has three number 21 chromosomes, resulting in Down syndrome
Genetics
study of where we get our genes and how
Gregor Mendel
Augustinian monk and botanist whose experiments in breeding garden peas led to his eventual recognition as founder of the science of genetics (1822-1884)
Trait
topic inherited from parents ex: hair color, eye color, heighy
Characteristic
expression of a trait ex: brown hair, blue eyes)
Genotype
genetic make-up of an organism
the 2 alleles inherited from your parents ex: Dd is a genotype for dimples
Phenotype
the expression of the genotype
appearance of a trait in an individual ex: DD= dimples dd= no dimples
Allele
alternative form of a gene.
Purebred
organisms from a distinct type or breed (tall w/ tall and short w/ short)
share similar traits
Hybrid
organism heterozygous for a trait
hybrid cross between 2 different purebred plants (tall w/ short)
Monohybrid cross
hybrid cross between 2 different purebred plants (tall w/ short)
Filial generation
offspring of a cross of parent organisms
P1, F1, F2
P1: parent generation, purebred plants F1: first filial generation, offspring from cross of P1 generation F2: second filial generation, offspring from cross of F1 generation
Dominant
trait that is always expressed
Recessive
trait that is not usually expressed but is still there
if its homozygous recessive it will be expressed
Homozygous
having the 2 same alleles for a trait (TT or tt)
Heterozygous
having 2 different alleles for a particular trait (Tt)
Codominance
both alleles are dominant and both are expressed ( spotty or checkered feathers)
Incomplete dominance
blending of two traits
neither alleles are dominant and a blend of the traits show (red and white genotypes express pink phenotypes)
Multiple allele inheritance
there are more than 2 alleles for that gene
Multiple gene inheritance
when a trait is controlled by more than 1 pair of genes
Carrier
individual who has an unhealthy/recessive allele on 1 part of the chromosome but doesn't express it
can pass it on to offspring
Law of segregation
traits are determined by pairs of alleles from each parent
offspring get one allele from each parent
Law of independent assortment
separate genes for separate traits are passed independently of one another from parent to offspring
Sex-linked traits
located on sex chromosomes
Pedigree
diagram that shows the occurrence of a genetic trait in several generations of a family
Synapsis
the side by side pairing of homologous maternal and paternal chromosomes at the start of meiosis
Autosome
Any chromosome that is not a sex chromosome (22 of 23)
X-linked
gene that is found on the X chromosome
mothers may be carriers and don't express the trait