Title: Bio 101 Test 6 Mitosis
1Bio 101 - Test 6 Mitosis Meiosis Ch 9
10Mendelian Genetics Ch 11Human heredity Ch
12
2About Chromosomes
- What is a chromosome?
- Eukaryotic DNA multiple linear diploid
chromosomes - Number of chromosomes (types) depends on species
- Chromosomes replicate
Unwound form of DNA Chromatin
3- Terms chromosome vs chromatid
chromatin vs condensed chromosome centro
mere vs centriole dulipcated
chromosome vs homologous pair - 2 cell types 1. somatic cell body diploid
2 sets 2. gamete sex cell M
F haploid 1 set - Human genome has 23 types of chromosome 22
autosomes 1 sex chromosome (23) human
conception 23M 23F 46 chromosomes NOTE
these are NOT stuck together NOT identical -
- How do corresponding M F chromosomes compare?
Same genes in same corresponding positionsbut
Are they exactly alike? Alleles different
forms of a gene
4Eukaryotic cell division
- 2 ways that Eukaryotic cells divide
1. Mitosis cell division
for growth, healing asexual repro. 1
diploid set ? 2 identical diploid sets (1 round) - somatic cells only somatic
cells genetically identical cloning? - 2. Meiosis cell division (2 rounds) for
gamete formation 1 diploid set ? 2 diploid
sets ? 4 haploid sets NOT identical
genetic variability strategy of sexual
reproduction - What is replication? It precedes cell division
46 X 2 92
?
?
? replication ?
5Cell cycle
90
Replication happens here 23 x 2 ? 23 x 2
x 2
6Mitosis Ch 9
- cell division for growth, healing asexual
repro. 1 diploid set ? 2 identical diploid
sets somatic cells - Interphase replication 90 of cycle
sochromatin - then Mitosis P M A T
- 1. Prophase chromatin condenses ? visible
chromosomes homologous pairs vs dupl.
chromosomes membrane breaks centrioles
move to poles -
Early prophase Late prophase
7more Mitosis
- 2. Metaphase replicated chromosomes line
up at equator end-to-end spindle fibers attach
to chromatids decision made -
- notice of fibers one per chromatid what
is going to get separated from what? so what is
a spindle fiber? Elastic connective tissue
and what if it gets old and loses its
elasticity?
Transition to metaphase
Metaphase
8and more still
- 3. Anaphase centromere breaks down
chromatids not held together fibers retract to
separate chromatids what is
being separated here? what is staying
together (NOT separated)? and remember
what happens when those fibers get old and
lose their elasticity?
9last one
- 4. Telophase centrioles back to original
position nuclear membrane forms x 2
- THEN..
- Cytokinesis cleavage furrow
..and we start over again
Telophase Cytokinesis
10How is Mitotic cell division controlled?
- Limited number telomeres clock - aging CNS?
vs skin - no? - Speed connective tissue vs skin
- Crowding contact inhibition monolayer
- Directional growth connective vs skin
- What else? Hormones ex. estrogen
Growth factors FGF Proteins ex
kinases Either induction or repression - Consider an embryo tissue differentiation
- Cancer loss of control abnormal cells?
How? Why? Malignant vs benign
Metastasized (systemic) vs contained
(local)
11Types of cancers NOT on test
- Carcinoma malignancies (M) derived from
epithelial cells most common forms of
breast, prostate, lung, colon cancers - Melanoma more rare but highly aggressive
carcinoma (?) - Lymphoma / leukemia M of blood / bone marrow
cells - Sarcoma M of connective tissue (other than
blood) - Mesothelioma M of respiratory mesothelium
asbestos - U.S. adult cancers male prostate 33 of
cases (Wikipedia) lung 31 of
deaths female breast 32 of
cases lung 27 of deaths - Good news? Most active most susceptible
Great progress is being made
12A new generation of anti-cancer drugs
NOT on test
- Angiogenesis inhibitor a sort of replication
inhibitor - Tyrosine kinase inhibitors prevent ATP
production prevent signal transduction - How do they find this stuff? Look for
unusual gene sequences, then. Look for
over-expression of particular genes
13Meiosis Ch 10
- cell division (2 rounds) for gamete formation
1 diploid set ? 2 diploid sets ? 4
haploid sets NOT identical genetic
variability strategy of sexual
reproduction - Interphasethen. P M A T.P M A T
meiosis 1 meiosis 2 2 (like
TWO) rounds of cell division Why? Do ya know?
Huh? Do ya? - 1 X 92 (interphase is interphase)
? 2 X 46 (NOT identical)
? 4 X 23 Haploid gametes
14- How is genetic variability assured in sexual
reproduction? 1. Crossing over when? Prophase
1 2. Independent assortment when? Metaphase
1 3. Random (?) combination of gametes - Prophase 1 chromatin condenses ? visible
chromosomes homologous pairs vs dupl.
chromosomes membrane breaks centrioles
move to poles ?AND. Replicated chromosomes line
up at equator but how? synapse
arrangement mom 1 next to dad 1etc - why? XX XX XX XX
15- What is crossing over? How does it work?
- The result? Swapped alleles between homologous
pairs - Would swapping alleles between chromatids
in a dupl. chromosome change anything?
So, vs Mitosis 1. Prophase is longer 2.
Side-by-side 3. Crossing over
16- Metaphase 1 Chromosomes already lined up
so all thats left to do is... Spindle fibers
attach notice of fibers (vs
Mitosis) one / dupl. chromosome what is
going to get separated from what? - The decision is made Independent
Assortment decision made independently at
each chromosome
So, vs mitosis
Metaphase is shorter
Metaphase 1 of meiosis
vs
XX XX XX XX
Metaphase - mitosis
17- Anaphase telophase similar to Mitosis
- Second round of cell division separates
chromatids one from another just like Mitosis
1st round 2nd round
18- Summary Mitosis vs Meiosis
- What cell types are involved? What are the
objectives? - Why are there 2 rounds of cell division in
Meiosis? - What is separated in each case? What stays
together? - Difference in the reason why they have 2 x 46?
- What is a zygote?
19Heredity Ch 11
- Transfer of traits from parent to offspring
inheritance - Gregor Mendel 1860 Austrian Monk / Botanist
- -conducted experiments breeding green pea
plants -he made various crosses and observed
inheritance of characteristic traits in the
offspring - -observed inheritance of consistent
predictable ratios - -fortunately the observed traits were
Mendelian 1. simple controlled by a single
gene 2. had only 2 alleles ex. flower
color 3. complete dominance relationships D
or R 4. his genes were NOT linked genes
control of observed traits on different
chromosomes
20- So what did Mendel really do (and he eventually
realized it)? True breeding purple x true
breeding purple True breeding white
x true breeding white but.. True breeding
purple x true breeding white and.
What if we cross 2 of these offspring? - Monohybrid cross Cc x Cc Phenotype
ratio 31 Genotpye ratio 121 - Punnett squares
- Genotypes homozygous dominant
CC homozygous recessive cc
heterozygous Cc
21- For Mendelian traits there were only 3
genotypes yielding only 2
phenotypes - From his work arose the Laws of Segregation
1. Traits are separated into packets which occur
in pairs 2. Two forms of each trait exist
dominant recessive 3. The forms segregate
randomly giving predictable ratios - In todays terminology. 1. Traits separated
into genes which are diploid 2.
Two alleles of each trait exist dominant
recessive 3. Alleles segregate randomly
giving predictable ratios - Keep in mind that Mendel only perceived the
phenotypes - Test cross used to determine genotype of
organism with dominant phenotype CC or Cc?
Cross with cc to find out.
22- Mendel found that alleles for the same gene can
segregate and recombine different
combinationsbut what about - Independent assortment A gene for 1 trait does
not influence (carry with) the gene for another
trait AS LONG as they are on separate chromosomes
(NOT linked) - flower color on chrom 1 A purple a
white plant height on chrom 2 B tall b
short - AB parent x ab parent just as likely to yield Ab
or aB ?
23- We can test this with a Dihybrid cross If
we cross AaBb X AaBb we get all possible
combinations Monohybrid cross gave P 31 G
121 Dihybrid cross gives P 9331
24- Single gene recessive disorders autosomal
disorders expressed only in homozygous
recessive individuals, with Heterozygous
individuals serving as carriers - Ex. 1 Albinoism P melanin p no
melanin - Consider normal parents that yield an albino
child 1. what is the genotype of both
parents? - 2. what is likelihood of the child being
albino? - Ex. 2 Sickle cell anemia H normal
hemoglobin h altered hemoglobin
- Ex. 3 Tay-Sachs disease a fatal condition
- how does the genotype ratio work on this
one? -
25All traits are not simple Mendelian traits
- 1. Incomplete dominance 3 genotypes
yield 3 phenotypes CC red Cc pink cc
white DONT think mixed Ex.
Cc X cc - 2. Co-dominance 2 of 3 alleles are
equally dominant 6 genotypes yield 4
phenotypes O is universal donor why?
26- 3. Pleiotropy 1 genotype yields many phenotypes
(symptoms) consider a gene controlling
something with global affects such as protein
production but which protein? Ex.
Sickle cell anemia PKU - 4. Epistasis epi upon 1 gene affect
expression of another Ex. albinoism
1 gene says melanin Yes or No
another group says, if Yes, how much - 5. Polygenic inheritance multiple genes
affect a single trait also called the
dosage affect Ex. skin
pigmentation 7 genes control greater dose of
dominant alleles darker skin pigmentation
27- 6. Multi-factorial traits nature vs nurture
Traits affected by both Genetic
Environmental influence No way to predict
phenotype other than empirical probability Dr.s
have kids that become Dr.s why? - Trait Environmental influence
- Consider height nutrition weight exerc
ise, nutrition intelligence nutrition,
friends, interests - heritability is a measure of the genetic
contribution to a multi-factorial trait on a
scale of 0 1. - Consider Similarity in MF trait in adoptee and
natural child Twins separated at birth yet
retain similarities - identical monozygotic same genes, same
sex - fraternal dizygotic no more similar than
any siblings
28Human genetics Ch 12
- Linked genes (vs slide 22) what if genes for 2
or more of Mendels pea traits HAD been on the
same chromosome? - would these genes be able to assort
independently? - would this prevent variability arising
from crossing over? - overall, how (much) would linkage affect
genetic variability? - Linkage map used to determine relative distance
between linked genes by measuring
frequency of gene separation via
crossing-over consider relative
likelihood of separating ? pink from
orange VS pink from green
29- Human sex determination chromosome 1
22 autosomes chromosome 23 is the sex
chromosome X or Y -
- ovum (X) sperm (X) XX female
homogametic ovum (X) sperm (Y) XY
male heterogametic - Sex-linked genes linked to X chromosome
Y X
30Genetic anomalies
- RememberSingle gene recessive disorders
- What about Sex-linked recessive disorders
almost always (we will say always) on X
chromosome who is most likely to inherit
these? can dad be a carrier? does dad
affect the son? what if mom is a carrier
and dad is normal? chance of son
expressing? chance of daughter expressing?
- Ex hemophilia, color blindness (G or R
cones), MD? - what if it is a terminal condition
male? female?
31- Abnormal chromosome number via
non-disjunction Aneuploidy wrong of a
particular chromosome can happen in 1st or 2nd
round of cell division monosomy worse than
trisomy autosomes worse than sex chromosome
Ex. Trisomy 21 Down syndrome or
mongolism - Polyploidy many copies wrong of
every chromosome actually can be a good
thing in plants Ex Triploid wheat
32Monitoring for genetic anomalies
- Alpha feta protein screening std. blood test by
law too high spina bifida incomplete
closure of spine too low Downs or other
aneuploidy - Amniocentesis gt 35 amniotic fluid drawn
from uterus genetic karyotype gives more
information, BUT carries some risk 1/200
spontaneous abortions - Chorionic Villus Sampling chorionic villi
(amnion forming tissue) sampled risk of
mortality low can do early on