Title: Mendelian Genetics
1Mendelian Genetics
2(No Transcript)
3Who Are You?
- Phenotype
- How you look PHysical appearance
- Genotype
- Your genetic makeup GENEs
4Father of Genetics
- Modern genetics began with Gregor Mendels
quantitative experiments with pea plants
Stamen
Carpel
Figure 9.2A, B
5- Mendel crossed pea plants that differed in
certain characteristics and traced the traits
from generation to generation
White
1
Removed stamensfrom purple flower
Stamens
Carpel
2
Transferred pollen from stamens of white flower
to carpel of purple flower
PARENTS(P)
Purple
3
Pollinated carpel matured into pod
- This illustration shows his technique for
cross-fertilization
4
Planted seeds from pod
OFF-SPRING(F1)
Figure 9.2C
6Genetics Basics
- Chromosomes occur in pairs, one from MOM, one
from DAD (homologues) - Genes are carried on chromosomes
- Genes code for a trait or characteristic (I.e.
hair color) - Alternate forms of that trait are called ALLELES
(ie. Blond, brown, redhead, etc)
7Alleles
- Alleles can be dominant or recessive
- Heterozygous vs. homozygous
- Only way to see a recessive trait?
8Mendel s basic laws
- Law of Segregation
-
- Law of Independent Assortment
9- The chromosomal basis of Mendels principles
Figure 9.17
10Walter Suttons Theory of Chromosomal
Inheritance(Mendels proof)
- Gametes contribute to heredity via nuclear
material (chromosomes) - Homologues segregate during meiosis
- Homologues separate independently of other
homologous pairs
11Probability
- Mathmatical model of how often specific events
will happen - of occurances/ of attempts
12Punnett Square
- Visual representation or model of
- what alleles can be present in gametes
- how those alleles can recombine in offspring
- Used to determine the probability of offsprings
genetic makeup
13Monohybrid Cross
- One gene
- 2 alleles considered (one from mom, one from dad
14Dihybrid Cross
- 2 genes
- 4 alleles considered
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16How can we determine Homo- vs. heterozygous
individuals?
- Test Cross
- Must use homo recessive to conduct cross in order
to see the questionable allele
17What Mendel Didnt See
- Multiple alleles
- Codominance
- Epistasis
- Polygenic traits or Continuous Variation
- Pleiotropy
- Incomplete Dominance or blended inheritance
- Environmental Effects
- Sex linked and sex influenced traits
18CoDominance
- Both alleles expressed at the same time both
dominant
19- Incomplete dominance neither allele is fully
dominant (blended inheritance)
Figure 9.12Ax
20Epistasis
- Sequential action of genes
- Product of one gene influences another (one gene
gives permission for another allele to work - Gene action acts as a biochemical pathway
feedback inhibition - Ex Indian corn coloration
21Pleiotropy
- Where one allele may have multiple effects on
phenotype -
22- Normal and sickle red blood cells
Figure 9.14x1
23Individual homozygousfor sickle-cell allele
Sickle-cell (abnormal) hemoglobin
Abnormal hemoglobin crystallizes,causing red
blood cells to become sickle-shaped
Sickle cells
Clumping of cells and clogging of small blood
vessels
Breakdown of red blood cells
Accumulation ofsickled cells in spleen
Heart failure
Pain and fever
Spleen damage
Physical weakness
Brain damage
Damage to other organs
Anemia
Impaired mental function
Pneumonia and other infections
Kidney failure
Rheumatism
Paralysis
24Continuous Variationor Polygenic Traits
- Multiple genes acting to influence a
characteristic - Produces gradual changes, not distinct borders
- Ie. Height, weight, nose length, skin pigment
25P GENERATION
aabbcc(very light)
AABBCC(very dark)
F1 GENERATION
AaBbCc
AaBbCc
Sperm
Fraction of population
Skin pigmentation
F2 GENERATION
Figure 9.16
26Environmental Influence
- Example color change of fur in arctic animals
27Same eyes, different lighting
28Multiple Alleles
- More than one allele per gene
29- 3 alleles (ABO)
- 4 phenotypes (A, B, AB, O)
- Uses concept of glycoproteins (sugar name tags or
antigens) to mark cells - Non-recognition of the correct name tag for
blood type can cause agglutination
30Landsteiner Blood Groups
- Type A galactosamine AA (homo) or AO (hetero)
- Type B galactose BB or BO
- Type AB galactosamine galactose (codominant)
- Type O no sugar marker - OO
31Blood Donor Facts
32Rh factor
- Rh factor can be or
- is like a seen name tag or antigen
- - is invisible
- Rh- moms that have Rh babies are subject to
spontaneous abortions - Erythroblastosis fetalis
- Controlled with an injectionof RhoGam to hide
babies cells
33Sex Linked
- Sex on the X
- Specific trait/disorder is found on sex
chromosome, usually the X - Usually recessive traits
- Seen more often in males than females
- Ex color blindness, hemophilia
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35Barr Body inactivation
- In females, both X chromosomes are not
metabolically active - Random inactivation of one X chromosome may
influence traits expressed