Unit 4
Chapter 12
centromere - narrow waist of the duplicated chromosome
sister chromatids will seperate
cytokinesis - division of the cytoplasm
binary fission - prokaryotes dividing
phosphorylate - bring to a higher energy state
Interphase
most of a cell’s life
G1 - duplicates cell parts; if it gets through G1 good chance of cell division
checkpoint - does it have enough stuff to synthesize DNA
either apoptosis or G0
most important
no dna damage, p53 is broken down
too much p53 initiates apoptosis
S - (synthesis) - duplicates chromosomes specifically
G2 - double checks DNA replication
checkpoint - did the cell make mistakes in making DNA
apoptosis or mitosis
M - mitosis and cytokinesis
checkpoint - checks if all sister chromatids are attached to the spindle microtubules
Cyclins and Cyclin dependent kinases
when the two link up they make mitosis promoting factor (MPF)
MPF is made of a cyclin, a Cdk (kinase) and a phosphate group
CDK always there, signal later breaks down the cyclin
Growth Factors
platelet-derived growth factor (PDGF)
platelets cause cells to clot
density dependent inhibition - when crowded cells send signal to stop dividing
anchorage dependence - must be attached to substratum in order to divide
blood cells do not have anchorage dependence because they are always moving
There are proteins or enzymes that are necessary to make things go
different checkpoints
Mitosis
prophase
prometaphase
metaphase
anaphase
telophase
Chapter 13
life cycle - birth to time of reproduction
human somatic cells - non reproductive cells
karyotype - ordered display of the chromosomes in a cell
homologous chromosome - chromosomes that have the same genes in the same positions
sex chromosomes - determine the sex of the individual, called x and y
remaining 22 chromosomes - autosomes
diploid cell - (2n) has two sets of
first diploid cell is a zygote
Meiosis I
first part of cycle
two daughter cells per round
reductional division
makes two different cells
Prophase 1
DNA has been copies
duplicated sister chromatids
Metaphase 1
crossing over - chiasmata
microtubules
Anaphase 1
can be pulled apart either color either way
Telophase 1 and Cytokinesis
each half of the cell has a haploid set of chromosomes
Meiosis II
like mitosis
no crossing over
no identical cells
end with 23 chromosomes in every cell
reduces the number of chromosomes from two of each to one of each
Plants
bryophytes
ferns
gymno
Four steps plant went through to dominate planet
movement onto land
bryophytes
tissues
true tissures, (ferns)
move water from roots to shoots, sint have to be small
gymnosperm
seed (conifer tree)
angiosperms
coevolved to insects, ability to reproduce
Genes
P generation - parental generation
F1 - hybrid offspring
Law of Segregation
ratio of 3:1 purple to white in F2
when gametes are produced, two copies of each allele segregate so that offspring inherit only one allele
Four concepts of Mendel
two different versions of genes and the alternate versions are called alleles
if the alleles differ, one is the dominant and one is recessive
law of segregation
possible combinations are shown using punnett square
Law of independent assortment - the allele a gamete receives for one gene does not influence the allele received for another gene
homozygous
heterozygous
phenotype - appearance
genotype - letters/genes
test-cross - breeding the mystery individual with a homozygous recessive individual
monohybrid cross - Hh x Hh
dihybrid cross - YRYr x YRYr
The phenotypic ratio will always be 9:3:3:1
complete dominance - dominant gene
codominance - mix
incomplete - both show up
Tay-Sachs: fatal disease, buildup of lipids in brain
Non-nuclear inheritance
disorders that come from the DNA in mitochondria
less energy
always comes from the mom
Pedigree Analysis
circles for females
square for males
shaded for affected
consanguineous (inbreeding) the recessive traits will show up more
Chapter 15
Thomas Hunt morgan studied fruit flies and figured out that some genes are linked and some are on sex chromosomes
only the males had white eyes (recessive) in F2 generation
proves the gene is on the x chromosome
x linked disorders are almost always, not usually y linked traits
The ultimate source of variations is mutations in the DNA
Nondisjunction is when chromosomes don't separate properly during cell division. This can cause genetic disorders because the cells end up with too many or too few chromosomes.
genomic imprinting - the silencing of certain genes that are stamped with an imprint during gamete production
Methylation is a process that happens in our bodies and other living things. It's like adding a small chemical tag called a methyl group to our DNA or proteins. This tag can change how our genes work, kind of like turning a switch on or off. It helps control which genes are active and which ones are not. Think of it as a way for our body to make different instructions for different cells, like telling them what to do and how to behave.