Beruflich Dokumente
Kultur Dokumente
0012
Understand the cell cycle, the stages and end of products of meiosis
and mitosis, and the role of cell division in unicellular and
multicellular organisms.
Fig. 12-1
Fig. 12-2
100 m
(a) Reproduction
20 m
200 m
Fig. 12-4
0.5 m
Chromosomes
Chromosome arm
Centromere
DNA molecules
Chromosome
duplication
(including DNA
synthesis)
Sister
chromatids
Separation of
sister chromatids
Centromere
Sister chromatids
Fig. 12-5
S
(DNA synthesis)
G1
M
it o
si
s
i
k
o
is
s
ne
t
y
C
M IT
(M) OTIC
PHA
SE
G2
Prometaphase
Metaphase
Anaphase
Telophase
Cytokinesis is well underway by late telophase
Fig. 12-6a
G2 of Interphase
Prophase
Prometaphase
Fig. 12-6b
G2 of Interphase
Chromatin
Centrosomes
(with centriole (duplicated)
pairs)
Prophase
Early mitotic Aster
spindle
Prometaphase
Centromere
Chromosome, consisting
of two sister chromatids
Fragments
of nuclear
envelope
Kinetochore
Nonkinetochore
microtubules
Kinetochore
microtubule
Fig. 12-6c
Metaphase
Anaphase
Fig. 12-6d
Metaphase
Anaphase
Metaphase
plate
Spindle
Centrosome at
one spindle pole
Daughter
chromosomes
Nuclear
envelope
forming
Nucleolus
forming
Fig. 12-7
Aster
Centrosome
Sister
chromatids
Microtubules
Chromosomes
Metaphase
plate
Kinetochores
Centrosome
1 m
Overlapping
nonkinetochore
microtubules
Kinetochore
microtubules
0.5 m
Fig. 12-9
100 m
Cleavage furrow
Contractile ring of
microfilaments
Vesicles
forming
cell plate
Wall of
parent cell
Cell plate
1 m
New cell wall
Daughter cells
Daughter cells
(b) Cell plate formation in a plant cell (TEM)
Fig. 12-10
Nucleus
Nucleolus
1 Prophase
Chromatin
condensing
Chromosomes
2 Prometaphase
3 Metaphase
Cell plate
4 Anaphase
5 Telophase
10 m
Binary Fission
Prokaryotes (bacteria and archaea) reproduce by a type of
cell division called binary fission
In binary fission, the chromosome replicates (beginning at the
origin of replication), and the two daughter chromosomes
actively move apart
Fig. 12-11-4
Origin of
replication
E. coli cell
Two copies
of origin
Origin
Cell wall
Plasma
membrane
Bacterial
chromosome
Origin
Fig. 12-14
G1 checkpoint
Control
system
G1
G2
M checkpoint
G2 checkpoint
If the cell does not receive the go-ahead signal, it will exit the
cycle, switching into a nondividing state called the G0 phase
Fig. 12-15
G0
G1 checkpoint
G1
(a) Cell receives a go-ahead
signal
G1
(b) Cell does not receive a
go-ahead signal
Fig. 12-18
Scalpels
Petri
plate
Without PDGF
cells fail to divide
With PDGF
cells proliferate
Cultured fibroblasts
10 m
Fig. 12-19
Anchorage dependence
Density-dependent inhibition
Density-dependent inhibition
25 m
25 m
Fig. 12-20
Lymph
vessel
Tumor
Blood
vessel
Cancer
cell
Metastatic
tumor
Glandular
tissue
1 A tumor grows
from a single
cancer cell.
2 Cancer cells
to other parts of
the body.
Fig. 12-UN1
G1
Cytokinesis
Mitosis
G2
Prophase
Telophase and
Cytokinesis
Prometaphase
Anaphase
Metaphase
Fig. 12-UN2
CHAPTER 13
Meiosis and Sexual
Life Cycles
Overview: Variations on a
Theme
Inheritance of Genes
Fig. 13-2a
0.5 mm
Parent
Bud
(a) Hydra
Fig. 13-3
APPLICATION
TECHNIQUE
5 m
Pair of homologous
replicated chromosomes
Centromere
Sister
Metaphase
chromatids
chromosome
Fig. 13-4
Key
2n = 6
Maternal set of
chromosomes (n = 3 )
Paternal set of
chromosomes (n = 3)
Two nonsister
chromatids in
a homologous pair
Centromere
Pair of homologous
chromosomes
(one from each set)
Life Cycle
Fig. 13-5
Key
Haploid gametes (n = 23)
Haploid (n)
Egg (n)
Diploid (2n)
Sperm (n)
MEIOSIS
FERTILIZATION
Testis
Ovary
Diploid
zygote
Mitosis and
development
Multicellular diploid
adults (2n = 46)
(2n = 46)
The three main types of sexual life cycles differ in the timing
of meiosis and fertilization
The two cell divisions result in four daughter cells, rather than
the two daughter cells in mitosis
Fig. 13-7-1
Interphase
Homologous pair of chromosomes
in diploid parent cell
Chromosomes
replicate
Homologous pair of replicated chromosomes
Sister
chromatids
Fig. 13-7-2
Interphase
Homologous pair of chromosomes
in diploid parent cell
Chromosomes
replicate
Homologous pair of replicated chromosomes
Sister
chromatids
Meiosis I
1Homologous
chromosomes
separate
Haploid cells with
replicated chromosomes
Fig. 13-7-3
Interphase
Homologous pair of chromosomes
in diploid parent cell
Chromosomes
replicate
Homologous pair of replicated chromosomes
Sister
chromatids
Meiosis I
1Homologous
chromosomes
separate
Haploid cells with
replicated chromosomes
Meiosis II
2 Sister chromatids
separate
Fig. 13-8
Metaphase I
Prophase I
Centrosome
(with centriole pair)
Sister
chromatids
Chiasmata
Spindle
Centromere
(with kinetochore)
Prophase II
Metaphase II
Anaphase II
Telophase II and
Cytokinesis
Sister chromatids
remain attached
Metaphase
plate
Homologous
chromosomes
separate
Homologous
chromosomes
Fragments
of nuclear
envelope
Telophase I and
Cytokinesis
Anaphase I
Microtubule
attached to
kinetochore
Cleavage
furrow
Sister chromatids
separate
Fig. 13-8a
Prophase I
Metaphase I
Centrosome
(with centriole pair)
Sister
chromatids
Chiasmata
Spindle
Centromere
(with kinetochore)
Sister chromatids
remain attached
Metaphase
plate
Homologous
chromosomes
separate
Homologous
chromosomes
Fragments
of nuclear
envelope
Telophase I and
Cytokinesis
Anaphase I
Microtubule
attached to
kinetochore
Cleavage
furrow
Fig. 13-8b
Prophase I
Metaphase I
Centrosome
(with centriole pair)
Sister
chromatids
Chiasmata
Spindle
Centromere
(with kinetochore)
Metaphase
plate
Homologous
chromosomes
Fragments
of nuclear
envelope
Microtubule
attached to
kinetochore
Fig. 13-8c
Telophase I and
Cytokinesis
Anaphase I
Sister chromatids
remain attached
Homologous
chromosomes
separate
Cleavage
furrow
Fig. 13-8d
Prophase II
Metaphase II
Anaphase II
Telophase II and
Cytokinesis
Sister chromatids
separate
Fig. 13-8e
Prophase II
Metaphase II
Fig. 13-8f
Anaphase II
Telephase II and
Cytokinesis
Sister chromatids
separate
Fig. 13-9a
MITOSIS
MEIOSIS
Parent cell
Chromosome
replication
Prophase
Chiasma
Chromosome
replication
Prophase I
Homologous
chromosome
pair
2n = 6
Replicated chromosome
MEIOSIS I
Metaphase
Metaphase I
Anaphase
Telophase
Anaphase I
Telophase I
Haploid
n=3
Daughter
cells of
meiosis I
2n
Daughter cells
of mitosis
2n
MEIOSIS II
n
n
n
n
Daughter cells of meiosis II
Fig. 13-9b
SUMMARY
Property
Mitosis
Meiosis
DNA
replication
Number of
divisions
Synapsis of
homologous
chromosomes
Number of
daughter cells
and genetic
composition
Role in the
animal body
8 million (223)
Fig. 13-11-3
Possibility 2
Possibility 1
Two equally probable
arrangements of
chromosomes at
metaphase I
Metaphase II
Daughter
cells
Combination 1 Combination 2
Combination 3 Combination 4
Crossing Over
Fig. 13-12-5
Prophase I
of meiosis
Pair of
homologs
Nonsister
chromatids
held together
during synapsis
Chiasma
Centromere
TEM
Anaphase I
Anaphase II
Daughter
cells
Recombinant chromosomes
Random Fertilization
Order of Content
1. DNA Isolation
2. Polymerase Chain Reaction
3. Gel Electrophoresis
4. Recombinant DNA
5. GMOs
Order of Content
1. DNA Isolation
2. Polymerase Chain Reaction
3. Gel Electrophoresis
4. Recombinant DNA
5. GMOs
DNA Isolation
This is the process of
extracting DNA from a
particular source of interest.
Isolation is necessary,
because DNA is housed inside
of the nucleus of the cell. In
order to extract the DNA from
the nucleus, the cell must be
broken down.
Order of Content
1. DNA Isolation
2. Polymerase Chain Reaction
3. Gel Electrophoresis
4. Recombinant DNA
5. GMOs
Components of PCR
DNA
Primers (These are specific to
your region of interest)
dNTPs (bases)
taq Polymerase (enzyme that
carries out the reaction)
Thermocycler (machine in
which PCR occurs)
Stages of PCR
1. Denaturation: the strands of DNA
separate from each other.
2. Annealing: primers will bind to the 3 ends
of the parent DNA strands.
3. Elongation: the new strand will synthesize.
This cycle repeats for as many times you
have specified, or until one of the
components run out.
** Cooling is the last and final step of PCR.
This only occurs after the last and final
cycle.
Order of Content
1. DNA Isolation
2. Polymerase Chain Reaction
3. Gel Electrophoresis
4. Recombinant DNA
5. GMOs
Gel Electrophoresis
Gel Electrophoresis allows us to visualize our
results from PCR.
Agarose is one of the more common gels
used in this technique.
It uses applied current to separate the DNA
based on both size and charge.
Since DNA is negatively charged, it will move
from the top (negatively charged end) of the
gel towards the bottom (positively charged
end).
The smaller the DNA fragment, the faster it
will move.
Order of Content
1. DNA Isolation
2. Polymerase Chain Reaction
3. Gel Electrophoresis
4. Recombinant DNA
5. GMOs
Recombinant DNA
Lab created DNA that
combines different sets of
DNA.
Uses a vector and an insert.
The insert is the DNA of
interest.
The vector is the cell that you
wish to insert your insert into.
Insulin
Production
Takes advantage of Recombinant
DNA techniques.
Cut out the human insulin gene with
restriction enzymes.
Insert it into a bacterial or yeast vector
that has been cut with the same
restriction enzymes.
Let it replicate to continuously produce
more insulin.
Genetically
Modified
Organisms
We have used DNA techniques to add
and remove/suppress particular genes
(GMOs)
in the foods that we eat.
Why would we want to do this?