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DNA packaging and cell reproduction
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prokaryotes
bacteria, archaea
always single-celled
small cells without membrane bound organelles
DNA is NOT packaged. It’s floating around in the cytoplasm
just 1 circular chromosome + many small circular plasmids
how is DNA packaged in prokaryotes?
NOT packaged!
in the cytoplasm
1 circular chromosome
eukaryotes
protists, fungi, plants, animals
can be single (protists) or multicelled
larger cells with membrane bound organelles
DNA packaged in the nucleus!!
^ also in the mitochondria and chloroplasts
where is DNA packaged in a eukaryotic cell and what is its structure like?
in the nucleus, mitochondria, and chloroplasts
nucleus: many linear chromosomes
mito. and chloro.: circular
how long would DNA from a human body be?
6.4 billion bases x 0.34nm between 2 bases
super long!!
we have about 50 trillion cells
how to prokaryotes fit all of their DNA into the cell?
supercoil their chromosomal DNA
positive supercoiling (over-twisting)
negative supercoiling (under-twisting)
DNA coils on itself!
topoisomerases
enzymes that add or remove rotations by breaking the DNA, rotating the ends, and rejoining the pieces
phosophodiester bonds are getting broken!
prokaryotic DNA is normally kept
negatively supercoiled
how do eukaryotes fit all of their DNA inside the cell?
DNA is packaged with proteins into chromatin and chromosomes
proteins = histones
levels of DNA packaging in eukaryotes
10nm fiber
30nm fiber
300nm fiber
700nm fiber (now its called a chromosome!!)
histones
small, positively charged proteins
why they’re positively charged: positive charge on R groups in the amino acid
lysine rich!!!
significance of histones being pos. charged
DNA is neg. charged, so attracted to histones/wants to interact
DNA wraps around histones!!
beads on a string
which histone proteins make up the histone core?
8 total!
2 each of:
H2A
H2B
H3
H4
*H1 acts as a linker protein!!
nucleosome
histone core (8 histones) + DNA wrapped around it
~146 bp of DNA wrapped around each histone
chromatin
DNA complexed with histones
10nm
30nm
300nm
linker DNA
about 50 bp between nucleosomes
30 nm level of DNA packaging
10 nm fiber coils around itself
6 nucleosomes per turn
H1 histone helps pull the nucleosomes together in a circle/ring
300 nm level of packaging
30nm chromatin fiber forms “looped domains” on a protein scaffold insidle the nuclear envelope
protein scaffold is not a histone
700 nm level of packaging
highest level!!
scaffold folds up on itself
no longer chromatin, but chromosome
best level of packaging for gene expression
1st level (10nm fiber)
as loosely packaged as possible!
2 types of chromatin
euchromatin: contains actively expressed genes (these are transcribed and translated)
10nm or 30nm fiber fall in this category
heterochromatin: few actively expressed genes
300nm fiber
for most part, shuts down gene expression
DNA within cells will be at one of the first 3 levels of packaging as chromatin when in this phase
interphase
before cell division occurs!!
mitotic chromosome
700nm fiber level
ready for cell division!
chromosome
a structure made of tightly packaged DNA and its associated proteins
700nm level, scaffold folding
gene
a discrete unit of heredity made of a specific sequence of DNA
contains the genetic info for a particular trait
multiple genes controlling different traits are contained on a chromosome
how many genes are on each of the 23 pairs of human chromosomes?
varies for each chromosome
in the hundred and thousands!
chromosomes are numbered based on their length
#1 is the longest and contains the most genes!
karyotype
visual display of the chromosomes of an individual/cell
purpose: identify large scale issues
missing or extra copies of chromosomes
can also determine gender from it!!
autosomes vs. sex chromosomes
22 pairs of autosomes (44 total)
1 pair of sex chromosomes
trisomy 21
3rd copy of chromosome 21
aka down syndrome
klinefelter syndrome
XXY
Turner syndrome
XO
only one X chromosome, that’s it!
1 “stick” in a karyotype would be called a
chromosome
homologous chromosomes / homologs
chromosomes that pair during meiosis and have an identical set of genes
ex: 2 copies of chromosome 2
are the DNA sequences of homologs identical?
no
have same genes located on them, but could have different alleles
heterologous chromosomes (non-homologs)
chromosomes containing different genes
do NOT pair during meiosis
ex: a copy of chromosome 3 and a copy of chromosome 4
allele
one of 2 or more alternate forms of a single gene
encode diff. forms of a chara
homologs can either be homozygous or heterozygous. what does this mean?
homozygous: the homologs have the same version of a specific allele
EX: AA
heterozygous: the homologs have different alleles
EX: Dd
what happens to chromosomes before cell division
every chromosome is replicated
look like an X once this happens
one X = one replicated chromosome
the individual lines making up the X (aka 1 replicated chromosome) are called
chromatids
sister chromatids
the 2 subunits of a replicated chromosome
they should be identical!
have same alleles!
non-sister chromatids
chromatids from different chromosomes
centromere
where chromatids remain attached
binary fission
cell division in prokaryotes
goal: exact copies of original cell, asexual reproduction
1 cycle every ~20 min
2 types of cell division in eukaryotes
mitosis and meiosis
purpose of mitosis
make identical copies of a cell
1 —→ 2
purpose of meiosis
reduce # of chromosomes
pull homologous pair apart
cells will have ½ the amount of DN
cells go from diploid to haploid
G1 in cell cycle
cell grows, prepare for DNA replication
check for any DNA damage before moving on to S phase to replicate
If can’t fix damage: apoptosis (programmed cell death)
S phase
all DNA replicated exactly 1 time
creates genetically identical sister chromatids
same # of chromosomes, 2x the DNA
interphase
G1,S,and G2
the preparation for cell division
DNA is in chromatin form
G0
cells that cease division/ do not go thru mitosis
phases of mitosis
prophase
prometaphase
metaphase
anaphase
telophase/cytokinesis
prophase
DNA condenses into chromosome form (700nm)
the spindle apparatus (mitotic spindle) forms
spindle fibers are made up of
microtubules
chromosomes are where during prophase?
the nucleus
prometaphase
nuclear envelope breaks down
spindle fibers indirectly attach to chromosomes (attach to the kinetochores)
what is a kinetochore
collection of proteins on the centromere
there’s 1 per chromatid
spindle fibers attach here during prometaphase
metaphase
chromosomes are pulled to the metaphase plate
homologs DO NOT interact
anaphase
the identical sister chromatids are pulled to opposite sides of the cell
no longer sisters. they are 2 identical “daughter chromosomes”
why is the metaphase to anaphase transition so important?
spindle fibers need to properly connect to the kinetochores of the sister chromatids so they can be properly/evenly pulled apart
don’t want an extra or missing chromosome in one of the daughter cells!
nondisjunction
when the sister chromatids don’t properly separate during anaphase
can lead to a trisomy or monosomy
cohesin
the “glue” that keeps sister chromatids together
breakdown of cohesin in the transition from meta to anaphase allows the sister chromatids to separate in anaphase
telophase and cytokinesis
spindle apparatus dissolves (microtubules dissociate)
nuclear envelopes form
chromosomes decondense (700nm —→ 300, 30, or 10) back to chromatin form!!
cell membrane divides the cell (cytokinesis)
result of mitosis
2 genetically identical daughter cells
identical to original/parent cell!
why do we need mitosis?
growth and development
repair
in anaphase, there are no more ______
chromatids
double the amount of chromosomes!
daughter chromosomes
ex: meta —→ ana: 4 ——> 8 chromosomes and 8 ——> 0 chromatids