Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
48 Cards in this Set
- Front
- Back
Prior to cell division, ______ are duplicated. Visible ______ consist of two identical sister chromatids attached at centromere. Once sister chromatids separate they are again called _______.
|
Chromosomes
|
|
Make up a chromosome and are to be separated during cell division.
|
Sister Chromatids
|
|
holds two sister chromatids together to make one chromosome.
|
Centromere
|
|
an enzyme that catalyzes the transfer of a phosphate group from ATP to another molecule. (Taking phosphate off stops the cell cycle). ____ works like turning off a light switch. CDK is a cyclin dependent ______.
|
Kinase
|
|
special chemicals that make the cell cycle go around; there are many different types. Elevated in breast cancer.
|
Cyclins
|
|
like an alarm clock, that tells the cell when it is time to do some essential activities and when to divide. Many chemicals inside the cell regulate it.
|
Cell Cycle
|
|
The complete set of chromosomes (46) is known as the ____ number in humans. Somatic Cells are ____.
|
Diploid
|
|
Sex cells are this.
|
Haploid
|
|
Pairs of genes segregate during gamete formation; fertilization pairs genes again.
|
Law of Segregation
|
|
random arrangement of
chromosomes on the metaphase plate. |
Law of Random Assortment
|
|
one gene influences many characteristics.
|
Pleiotropy
|
|
one allele interferes with the expression of another allele.
|
Epistasis
|
|
many genes influence one characteristic
|
Polygenic Inheritance
|
|
one allele is not completely dominant over another. Ex- red + white = pink.
|
Incomplete Dominance
|
|
more then two alleles for one trait. Ex- Blood types: A, B, O.
|
Multiple Alleles
|
|
both dominant alleles are expressed equally. Ex- Blood type AB.
|
Codominance
|
|
2 different alleles. Ex- Bb. b is the disease carrier, always recessive.
|
Heterozygous
|
|
2 of the same allele. Dominant= BB, Recessive= bb. AKA true breeding.
|
Homozygous
|
|
one allele. Ex- males only: XY.
|
Hemizygous
|
|
only in females, 45 chromosome, genotype XO.
|
Turner's Syndrome
|
|
inactive x chromosome. XXX. One of the X’s is randomly selected to be turned off.
|
Barr Body
|
|
only in males, 47 chromosome, genotype XY.
|
Klinefelters
|
|
an abnormal number of chromosomes, extra or less.
|
Anueploidy
|
|
chromosome number 21 is affected. Has one extra chromosome, should have two.
|
Down Syndrome
|
|
a display (picture) of chromosome pairs.
|
Karyotype
|
|
XX or XY
|
Sex Linked
|
|
Independent of chromosomes. Ie: BB, Bb, or bb
|
Autosomal
|
|
location of a gene or allele on a chromosome.
|
Locus
|
|
physical characteristics
|
Phenotype
|
|
genetic makeup
|
Genotype
|
|
when cells meet, they stop dividing.
|
Density Dependent Inhibition
|
|
cell enters if it is damaged. Some cells are permanently in here. (Brain Cells) No cell division occurs here.
|
G0
|
|
master tumor suppressor gene in your body. One copy from mom, one from dad. This gene interacts with your cell cycle. Defect= Li- Fraumeni Syndrome.
|
P53
|
|
In families, very rare, predisposition to cancer. P53 problem, has multiple forms.
|
Li Fraumeni Syndrome
|
|
cell suicide. If so much DNA damage occurs and cells cannot fix it. (Use G0). Ex- sunburn.
|
Apoptosis
|
|
for n chromosomes, there are two different combinations of this of haploid pairs. For humans, 223 different combinations and 64 billion combinations at fertilization.
|
2^n
|
|
dealing with a single trait. Ex- just hair color.
|
Monohybrid
|
|
dealing with two traits at the same time. Ex- hair and eye color.
|
Dihybrid
|
|
two of the same genes for one characteristic. Ex- WW or ww.
|
True Breeding
|
|
same as Tay-Sacs disease. (incomplete dominance)
|
Sickle Cell Anemia
|
|
assists scientists in determinations of transmission of traits/diseases in families.
|
Pedigree
|
|
do not follow Mendelian inheritance because guys are XY.
|
Sex-Linked Genes
|
|
more than two complete sets of chromosomes.
|
Polyploidy
|
|
an exception to the chromosomal theory of inheritance. Individuals do this in gamete cells during meiosis and it affects expression in offspring.
|
Genomic Imprinting
|
|
homologous chromosomes synapse and form this.
|
Tetrad
|
|
are pairs of chromosomes, one from each parent.
|
Homologous Chromosome
|
|
either free end of a chromosome, sticky end with DNA.
|
Telomere
|
|
the side by side pairing of homologous maternal and paternal chromosomes, aka _______, is the start of meiosis.
|
Synapsis
|