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Cell Cycle/ Genetics

Gregor Mendel first to accurately describe rules of inheritance
P generation parents you start with, usually homozygous
dominant an allele that is expressed whenever it is present
recessive an allele that is masked whenever the dominant allele is present, expressed when two recessive allele are present
genotype specific genes for a particular trait
phenotype physical appearance of the gene
punnet square graphic way to predict possible outcomes of a cross
homozygous 2 identical alleles ex. AA
heterozygous 2 different alleles ex. Aa
genotype ratio number of offspring with the same genotype
phenotype ratio number of offspring with the same physical appearance
dihybrid cross experimental cross usually involving parents that are homozygous for two different traits
incomplete dominance heterozygote has intermediate phenotype ex. wavy hair intermediate of straight and curly
female XX
male XY
sex-linked traits genes located on one of the gametes (usually the X since it is bigger than the Y)
zygote fusion of an egg and sperm cell
cell division done when a cell splits into two daughter cells, also called cell reproduction
Humans have ___ chromosomes 46 or 23 pairs
chromatin fibers of equal parts DNA and protein molecules, not visible until cell division
cell cycle sequence of events that extend from a cell being formed to it's on division
phases of cell division interphase, mitosis, and cytokinesis
interphase part of cell division where replication occurs; Happens in 3 parts G1, S (synthesis), and G2
G1 cell grows and organelles duplicate
S (synthesis) DNA replicates
G2 cell makes protein needed for mitosis
mitosis when the cell divides into two daughter cells happens in 4 stages: prophase, metaphase, anaphase, and telophase
Prophase nuclear membrane disappears, centrioles appear and start to spread to opposite poles, chromatids appear and are attached to centromeres
metaphase chromatids line up in center of the cell still attached to centromeres
anaphase chromatids divide at centromere and pull apart to opposite poles
telophase nuclear membrane reforms around chromatids, centrioles and spindle fibers dissolve
cytokinesis the cell divides resulting in two daughter cells
cell cycle control system Regulates the cell cycle at various check points during interphase to make sure the cell is ready to divide, if checkpoints aren't passed cell will not divide
G1 checkpoint makes sure the cell is large enough to divide
S checkpoint makes sure DNA is properly replicate
metaphase/anaphase checkpoint in between the metaphase and anaphase, chromatids must be attached to spindles
contact inhibition cells stop dividing when it touches another cell
cancer cells that do not respond to the cell cycle control system, they lack contact inhibition and just keep dividing, can move to other locations in the body
tumors abnormally growing cell masses
growth factor simulates cells to divide
mutation change in the DNA, may be caused by error during synthesis or a mutagen
benign tumors abnormal cells at original site that may or my not be cancerous
metastasis spread of cancer cells beyond their original site through the circulatory or lymphatic system
malignant tumors can spread to other parts of the body
carcinogen something that causes cancer
mutagen causes a mutation
meiosis reduces the chromosome number from diploid to haploid same as mitosis but with repeating stages, and shuffles chromosomes
homologous chromosomes a pair of chromosomes that contain the same gene for the same trait, may contain different versions of the same gene
life cycle all the reproductive events that occur from one generation to the next
somatic cells body cells that are diploid
Meiosis 1 separates the homologous pairs into 2 separate cells, same four stages as mitosis
Meiosis 2 divides the sister chromatids into 4 haploid cells, same four stages as mitosis
synapsis occurs in prophase 1 of meiosis, the homologous pairs line up resulting in a tetrad
nondisjunction failure of homologous pairs to properly separate during meiosis, results in gamete having on too many or one too few chromosomes, most nondisjunction are not survivable
amniocentesis at 15-18 weeks gestation cells are drawn from the amniotic sac and cultured, stained, and examined, to check for any chromosomal disorders
trisomy 3 copies of the same chromosome
monosomy one copy of a chromosome
tri-21 trisomy of chromosome 21, known as down syndrome
turner syndrome one copy of female sex chromosome
klinefelter syndrome 2 copies of the female sex chromosome and one copy of the male sex chromosome
Created by: geneen23
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