Title: Chapters: 12-15
1Cell Division and Genetics
2Why do we need cell division?
- 2 REASONS
- Growth and maintenance
- Reproduction
3Cell Cycle Overview
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lCycle_L.jpg/252096666/CellCycle_L.jpg
4The Cell Cycle Control System
- A cyclically operating set of molecules in the
cell that both triggers and coordinates key
events in the cell cycle - regulated at certain checkpoints by both internal
and external signals
5The Checkpoints
- A control point where stop and go-ahead signals
can regulate the cycle - animal cells have built-in stop signals that halt
the cell cycle at checkpoints until overridden by
go ahead signals - signals come from cellular surveillance
mechanisms inside the cell - determine if the major processes of the cell
cycle have been completed - Three major check points G1, G2, M
6G1 Checkpoint
- Restriction Point"
- if a cell receives the go ahead at G1 checkpoint,
then the cell will continue with the cell cycle. - If the cell DOES NOT get the go ahead it will
enter G0 - the nondividing state of a cell
- most cells in body are in G0 (nerves and muscle
cells) - liver cells can be taken out of G0 phase if
necessary (growth factors released during injury)
7The Cell Cycle Clock
- The cell cycle is controlled by fluctuations of
cycle control molecules that occur in intervals - these rhythmic abundances pace the events of the
cell cycle - Regulatory molecules are two proteins
- cyclins
- protein kinase
- enzymes that will activate or inactivate other
proteins by phosphorylating them - give the go ahead signal at the G1 and G2
checkpoints
8Cell Division in Prokaryotes
- Called Binary Fission
- means "division in half" (asexual reproduction)
- starts at the origin of replication where the
circular DNA begins replicating - once the DNA is fully replicated, the cell begins
to stretch toward the poles of the cell - the membrane begins pinching off in the middle
- you now have two new daughter cells
9Interphase
- the longest phase of the cell cycle
- accounts for 90 of the cell's life
- the cell is producing proteins and cytoplasmic
organelles - The chromatin is not condensed during interphase
because it is needed for protein synthesis - Divided into 3 subphases
- G1 Phase gt first gap
- S Phase gt synthesis (chromosome duplication)
- G2 Phase gt second gap
-
10Mitosis
- The part of the cell cycle where the cell is
actually undergoing cell division - Consists of 5 stages
- prophase
- metaphase
- anaphase
- telophase
- Timing and rate of cell division are crucial to
normal growth, development and maitenance - varies with type of cell
- Cytokinesis is part of the Mitotic (M) phase, but
not apart of mitosis itself. - Different in plants and animals
11Prophase
- 1st stage of mitosis
- the chromatin condenses into two identical
chromosomes and the nuclear envelope begins to
disappear
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12Metaphase
- 2nd stage of mitosis
- the chromosomes line up on the equatorial plate
- spindle fibers are attached to the kinetochore of
each chromosome pair - "tug of war"
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13Anaphase
- 4th stage of mitosis
- shortest
- cohesion proteins are cut and the sister
chromatids are now separated - the cell beings elongating
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14Telophase
- Final stage of mitosis
- daughter cells begin to form
- nuclear envelope is visible again
- nucleoli reappear
- spindle fibers disappear
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15Comparing Cytokinesis
Animals
Plants
- There is NO cleavage furrow
- because plant cells have cell walls in addition
to cell membranes, they need to build a new cell
wall - vesicles will form in the middle of the original
parent cell from the golgi apparatus (starts
during telophase) - merge and become the cell plate
- enlarges until the membranes fuse
- In animals
- occurs by cleavage
- a cleavage furrow will form in what was the
middle of the parent cell - the furrow is a contractile ring of actin
filaments that contract - eventually splits the cell into two daughter
cells
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16Cyclins and Protein Kinases
- Timing of the cell cycle is initiated by growth
factors and controlled by two kinds of molecules
cyclins and protein kinases - protein kinases (cell signal transduction)
catalyze the phosphorylation of target proteins
that regulate the cell cycle - Cyclin-dependent kinases (CDKs)
17Cyclin-dependent Kinase
- Activated by binding to the protein cyclin
- exposes the active site to the CDK and activates
the molecule - allosteric regulation
- Several CDKs regulate the cell cycle at specific
stages called cell cycle checkpoints - each cyclin is manufactured at a precise time
during the cell cycle and therefore each CDK is
activated at a precise time - The activity of CDKs rises and falls with changes
in the concentration of its cyclin partner MPF
18The Chain Reaction that Controls the Cell Cycle
Cell Cycle events
CDK activation
growth factor
cyclin synthesis
19Meiosis
- this video made us laugh, if you get the gist
of it, move on - http//www.youtube.com/watch?viCL6d0OwKt8
20Meiosis Different than Mitosis
- Meiosis generates the genetic diversity taht is
the raw material for natural selection and
evolution - produces gametes (egg and sperm) or sex cells
- that are haploid the chromosome number (n) of the
parent cell - the chromosome number will return to diploid (2n)
during sexual fusion - NOT MITOSIS TWICE
21Meiosis I The Source of Genetic Variation
- Known as reduction division
- Meiosis I is characterized by
- homologous chromosomes pairing up
- crossing over genetic information
- the nonsister chromatids exchange genetic
information - results in recombination of genetic material
- CROSSING OVER ENSURES GREATER VARIATION AMONG
GAMETES
22Meiosis Prophase I
- Synapsis the pairing of homologous chromosomes
occur - crossing over occurs
- Chiasmata the point where the crossing over
occurs
23Prophase vs. Prophase I
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chiasmata
- Prophase Mitosis
- the chromosomes condense and sister chromatids
meet at the kinetochore
- Prophase I Meiosis
- homologous chromosomes pair up
- non-sister chromatids exchange genetic
information (crossing over) at the chiasmata
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24Meiosis I Overview
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25Meiosis II
- Meiosis II is exactly like mitosis in the sense
that the sister chromatids are separating and
forming two new cells - remember that after Meiosis I, there are two
haploid cells (half of the number of chromosomes)
that are genetically different - meiosis II continues as cell division, separating
the sister chromatids - In the end, each gamete should have half the
chromosomes of the parent cell and no sister
chromatids
26Egg sex cells vs. Sperm cells
- Male sex cells (sperm)
- undergo meiosis where each sperm is equal
- like you think a normal cell would undergo
meiosis - quantity over quality
- Female sex cells (eggs)
- specialized meiosis
- an egg will undergo meiosis to "get rid of" half
of genetic material, but will keep the rest of
the cells resources - leftover cells are called polar bodies
- quality over quantity
27Egg cells vs sperm cells
http//veterinary-online.blogspot.com/2012/12/deve
lopment-of-animals-formation-of.html.UX86879qpNY
28Ch. 14 Mendel and the Gene Idea
29Law of Dominance
- Mendels first law is the law of dominance
- Law of dominance states that when two organisms,
each homozygous (pure) for two opposing traits
are crossed, the offspring will be hybrid (carry
two different alleles) but will exhibit only the
dominant trait - The trait that remains hidden is known as the
recessive trait
Parent (P) TT X tt
(pure tall) (pure
dwarf) Offspring (F1) Tt
All hybrid
T
T
Tt Tt
Tt Tt
t
t
Law of dominance
All offspring are tall
30Law of Segregation
- The law of segregation states that during the
formation of gametes, the two traits carried by
each parent separate -
Gametes - The cross that best exemplifies this law the
monohybrid cross, Tt X Tt. In the monohybrid
cross, a trait that was not evident in either
parent appears in the F1 generation
Tt
T
t
31Law of Independent Assortment
- The only factor that determines how these alleles
segregate or assort is how the homologous pairs
line up in metaphase of meiosis I, which is
random.
http//2.bp.blogspot.com/-J9gE_FJmHIc/TZZc9lsPQhI/
AAAAAAAAACE/KuMgphh-1jU/s1600/science10.png
32Law of Independent Assortment
- The law of independent assortment applies when a
cross is carried out between two individuals
hybrids for two or more traits that are not on
the same chromosome. - This cross is called the dihybrid cross.
- This law states that during gamete formation, the
alleles of a gene for one trait segregate
independently from the allele of a gene for
another trait.
33Multiplication Rule
- Multiply the chance of one happening by the
chance that the other will happen - For example
- The chance of a couple having two boys depends on
two independent events. The chance of the first
child being a boy is ½ and the chance of the
next child being a boy is ½ - Therefore, the chance that the couple will have
two boy is ½ x ½ ¼ - The chance of having three boys is ½ x ½ x ½
1/8
34Addition Rule
- When more than one arrangement of events
producing the specified outcome is possible, the
probabilities for each outcome are added
together. - For example if a couple is planning on having
two children, what is the chance that they will
have one boy and one girl - The probability of having a girl and then a boy
is ½ x ½ ½ - The probability of having one boy and one girl is
¼ ¼ ½
35Monohybrid cross
- The monohybrid cross (Tt XTt) is a cross between
two organisms that are each hybrid for one trait.
- The phenotype (appearance) ration from this cross
is 3 tall to 1 dwarf plant. - The genotype (type of genes) ratio, 1 to 2 to 1,
given as percentages 25 homozygous dominant,
50 heterozygous, and 25 homozygous recessive.
These results are always the same for any
monohybrid cross.
T
t
TT Tt
Tt tt
T
F1 Tt X Tt F2 TT, Tt, or tt
t
Monohybrid cross
36Testcross
- The testcross is way to determine the genotype of
an individual plant or animal showing only the
dominant trait. - If the parent of unknown genotype is BB, there
can be no white offspring - B black
- b white
- If the parent of the unknown genotype is hybrid,
there is a 50 chance that any offspring will be
white.
B
B
Bb Bb
Bb Bb
b
b
B
b
Bb bb
Bb bb
b
b
37The Dihybrid Cross
- A dihybrid cross is a cross between two F1 plants
because it is a cross between individual that are
hybrid fro two different traits - This cross can produce 4 different types of
gametes, such as TY, Ty, tY, and ty.
tY
ty
TY
Ty
TTYY TTYy TtYy TtYy
TtYy TTyy TtYy Ttyy
TtYY TtYy ttYY ttYy
TtYy Ttyy ttYY ttyy
TY
Ty
tY
Phenotype ratio 9331
ty
38Incomplete dominance
- Incomplete dominance is characterized by
blending. - For example A red flower (RR) crossed with a
white flower (WW) produces all pink offspring
(RW)
R
R
RW RW
RW RW
W
W
R
W
- If 2 pink flowers are crossed, there is a 25
chance that the offspring will be red, a 25
chance the offspring will be white, and a 50
chance the offspring will be pink
RR RW
RW WW
R
W
39Codominance
- In codominance, both traits show.
- For example Different blood groups M, N, and MN
MM
NN
MN
40Multiple alleles
- Occurs when there are are more than two allelic
forms of a gene - For example Human blood types- A, B, AB and O
- The 3 alleles A, B, and O
- determine 4 different blood types
Human Blood Types Genotypes
Blood Type Genotype
A Homozygous A AA
A Hybrid A Ai
B Homozygous B BB
B Hybrid B Bi
AB AB
O ii
41Gene InteractionsPleiotropy
- Pleiotropy is the ability of one single gene to
affect an organism in several or many ways. - For example autosomal recessive disease cystic
fibrosis? abnormal thickening to mucus that coats
certain cells - ? thick mucus builds up in the pancreas, lungs,
digestive tract and other organs - leads to multiple pleiotropic effects including
poor absorption of nutrients in the intestine and
chronic bronchitis
42Gene Interactions Epistasis
- Where two separate genes control one trait, but
one gene masks the expression of the other gene - The gene that masks the expression of the other
gene is epistatic to the gene it masks - For example agouti coat color in mice?
- 2 genes control different enzymes in 2 different
pathways that both contribute to coat color - Both genes A and B must be present in order to
produce that agouti color
AB aB Ab ab
AB A/A B/ B Agouti A/a B/B Agouti A/A B/b Agouti A/a B/b Agouti
aB A/ a B/ B Agouti a/a B/B Black A/a B/b Agouti a/a B/b Black
Ab A/A B/b Agouti A/a B/B Agouti A/A b/b Albino A/a b/b Abino
ab A/a B/b Agouti a/a B/b Black A/a b/b Albino a/a b/b Albino
AaBb X AaBb
?In the absence of B, even if A is present, the
coat is colorless (albino) ?Therefore gene B is
epistasis to gene A
43Polygenic Inheritance
- Polygenic traits many characteristics such as
skin color, hair color, and height result from
blending of several separate genes that vary
along a continuum - The wide variation in genotypes always results in
a bell-shaped curve in an entire population
http//photos1.blogger.com/blogger/4252/2243/400/S
kin_Pigmentation.jpg
44The Pedigree
- A pedigree is a family tree that indicates the
phenotype of one trait being studied for every
member of a family - It can determine how a particular trait is
inherited - Females are represented by a and males
by a - A shape is completely shaded
in if a person exhibits the trait
http//www.oculist.net/downaton502/prof/ebook/duan
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45Ch. 15The Chromosomal Basis of Inheritance
46The Chromosomal Basis of Inheritance
- Chromosome theory of inheritance
- Genes have specific loci along chromosomes
- Chromosomes undergo segregation and independent
assortment
47Thomas Hunt Morgan's Experiment
- Fruit fly (drosophila melanogaster)
- Bred flies for 2 years with no conclusion
- Finally, 1 male had white eyes instead of the
usual red (red is the wild type-- characteristic
most commonly observed) - White eyes were a mutant phenotype
- Continued mating females with white-eyed male
- Discovered the gene for eye color is gender
related and on the X chromosome - Supported chromosome theory of inheritance that a
specific gene is on a specific chromosome
http//en.wikipedia.org/wiki/FileSexlinked_inheri
tance_white.jpg
48Sex-linked genes
- X and Y chromosomes
- XX-- female XY-- male (sex determination is
50-50 chance) - Sex-linked gene- gene located on either X
chromosome - Very few Y-linked genes, passed from father to
son - About 1,100 X-linked genes
- Males more likely to have disorders from X-linked
gene (have disease if either recessive or
dominant because only one X chromosome) - ex. color blindness, Duchenne muscular dystrophy,
hemophilia
49Sex-linked Genes
- X inactivation in Females
- Most of one X chromosome becomes inactivated when
embryo is developing - If did not become inactivated, chromosomes would
make 2x the amount of proteins for X-linked genes
as males - Inactive X condenses into compact object called a
Barr Body - Selection for which X chromosome is inactivated
occurs randomly
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50Linked Genes
- Linked genes- genes located near each other on
the same chromosome tend to be inherited together
in a genetic cross - Genetic recombination- the production of
offspring with combinations of traits that differ
from those found in either parent - Parental type- the half of the offspring that
inherit a phenotype that matches either parent's
phenotype - Recombinant types (recombinants)- offspring that
have non parental phenotypes
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51Gene Recombination and Linkage
- The physical basis of recombination between
unlinked genes is the random orientation of
homologous chromosomes - Happens in metaphase I of meiosis
- Leads to independent assortment of the 2 unlinked
genes - Crossing over- reciprocal exchange of genes
between one paternal and one maternal chromatid. - accounts for the recombination of linked genes
52Gene Recombination and Linkage
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53Alterations of Chromosomes
- Large-scale chromosomal changes can affect an
organism's phenotype - physical/ chemical disturbances or error during
meiosis - results in developmental disorders
- Nondisjunction- members of a pair of homologous
chromosomes don't move apart properly during
meiosis I or sister chromatids fail to separate
during meiosis II
http//www.nature.com/scitable/content/32851/10.10
38_nrm1526-f1_large_2.jpg
54Nondisjunction
- Aneuploidy- a condition where a normal gamete
unites with an abnormal one, resulting in a
zygote with an irregular amount of chromosomes - Monosomic- missing a chromosome (2n-1)
- Trisomic- chromosome tripled (2n1)
- If organism survives, has a set of traits that
result from abnormal amount or missing chromosome - ex. Down Syndrome (trisomy)
- Nondisjunction can occur during mitosis as well
- If happens during embryonic development, mitosis
will pass aneuploid condition to large number of
cells
55Nondisjunction
- Polyploidy-general term for chromosomal
alteration where organism has two complete
chromosome sets - triploidy (3n) tetraploidy (4n)
- More common in plants
- Have less effect than aneuploids because is a
full set of chromosomes and one missing
chromosome disrupts genetic balance more -
56Alterations in Chromosome Structure
- Error in meiosis or damaging agents can in 4
types of changes in chromosome structure - Deletion- when a chromosome fragment is lost
- Results in chromosome missing certain genes
- Duplication- the "deleted" fragment becomes
attached as an extra segment to a sister
chromatid - Inversion- chromosome fragment reattaches to the
original chromosome, but in the reverse
orientation - Translocation- fragment joins a nonhomologous
chromosome - Deletions and duplications are likely to occur
during meiosis (in crossing over)
57Alterations of Chromosome Structure
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58Genomic Imprinting
- Genomic Imprinting- Idea that the expression of
an allele in offspring depends on whether the
allele is inherited from the mother or father - Genes are autosomal (not sex-linked)
- Zygote only expresses one allele of an imprinted
gene, from mother or father - Occurs during gamete formation and results in the
silencing of particular alleles - Only affects a small fraction of gene in
mammalian genomes, but are usually genes critical
for development
59Organelle genes
- Extranuclear/cytoplasmic
- genes
- Genes located outside the nucleus
- Can be in mitochondria, chloroplast
- Are not distributed to offspring like with
nuclear chromosomes - Extranuclear genes first noticed by Karl Correns
(1909) - Noticed inheritance of yellow and white patches
on the leaves of a green plant - Coloration only determined by the maternal plant
- Research showed that coloration patterns are due
to mutations in genes that control pigmentation
http//s3.amazonaws.com/picable/2009/07/23/1195661
_Lovely-green-Plant_620.jpg
60Sources
- Goldberg, Deborah M.S. Barron's AP Biology. 3rd
ed. New York Baron's Educational Series, 2013.
Print. - Reece, Jane B., and Neil A. Campbell. Campbell
Biology. 9th ed. Boston Benjamin Cummings /
Pearson Education, 2011. Print.