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Who was Gregor Mendel?

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Title: Who was Gregor Mendel?


1
Who was Gregor Mendel?
  • Father of Genetics
  • Austrian monk, teacher, scientist and gardener
    who formulated basic laws of heredity in the
    early 1860s video

2
What did he study?
  • Worked with garden peas
  • Easy to grow and had a
  • short generation time video

3
Mendelian Genetics p68
Warm up why did Mendel choose pea plants to
study?
  • Mendel cross pollinated parent (P1) plants to
    produce new hybrids.
  • He crossed tall plants with short ones and the
    offspring (F1) were all tall.
  • Then he allowed the hybrids to self pollinate and
    got 3 tall and 1 short offspring (F2)

4
Conclusions? p68
  • Rule of unit factors we have 2 alleles
    (different gene forms) for each of our traits. (1
    from each parent)
  • Rule of Dominance one of our alleles is dominant
    (T) and one is recessive (t).
  • Law of segregation Independent Assortment
    during fertilization, both alleles from each
    parent randomly separate and combine in new ways.

5
Mendels Conclusion Paragraph p67
  • Explain how Mendel came up with each of his 3
    conclusions from his work with pea plants.

6
Examples of dominant and recessive traits in
humans! p70
7
More terminology p70
  • warm up describe some dominant and recessive
    traits you have.
  • Genotype refers to the alleles an individual
    receives at fertilization
  • Phenotype refers to the physical appearance
  • of the individual.
  • Homozygous dominant genotypes
  • two dominant alleles for a trait. (BB)
  • Homozygous recessive genotypes
  • possess two recessive alleles for a trait (bb)
  • Heterozygous genotypes
  • one of each allele for a particular trait (Bb)

8
Punnett Squares p70
  • Monohybrid Cross 1 trait, 2 parents

P1 Pure Tall x Pure Short TTTall tt short
F225 pure tall 50 hybrid tall 25
pure short
F1100 Tall
9
Dihybrid Cross 2 traits, parents p72
  • Warm up how many boxes are in a monohybrid cross
    and what does each box represent?

Dominant Yy, YY yellow Rr, RR round
Recessive yy green rr wrinkled
10
Each box is6.25
11
Recessive Allele Disorders p74
  • Warm up Describe a genetic disease that you have
    heard of or that someone you know has.
  • Disorder PKU
  • Facts missing an enzyme that breaks down
    Phenyalanine (in milk) it accumulates in the
    central nervous system
  • Caused by a point mutation
  • Symptoms can cause mental retardation, abnormal
    growth patterns
  • Incidence rare in African Americans Japanese
  • more common in Irish
  • Treatments test newborns- change diet

12
Recessive Disorders p74
  • Disorder CF- Cystic Fibrosis
  • Facts mucus in lungs digestive tract is very
    thick caused by point mutation
  • Symptoms makes breathing digestion difficult
  • Incidence most common in Caucasians(whites) 1
    in 2000 white 1 in 25 carry recessive allele.
  • Treatments frequent lungs infections, daily
    therapy is needed to loosen remove mucus

13
Recessive Disorders p74
  • Disorder Tay-Sachs
  • Facts disorder of central nervous system, brain
    spinal cord
  • missing an enzyme which breaks down lipids
    accumulates in brain
  • Symptoms everything goes in reverse
    deteriorates
  • Incidence 1 in 27 Jews, Cajuns(Lousiana),
    French-Canadians are carriers
  • Treatments none happens within 1st year most
    children dont live past 5

14
Defend your position p73
  • Q. If you were a scientist, which disease would
    you want to cure and why? (half page)
  • Q Explain why you agree or dont agree with the
    following statement We have millions of genes,
    so a mutation in one of them cant cause very
    much damage.

15
Incomplete Dominance p76
  • Warm up what does dominance mean? Incomplete?
    Codominance?
  • When 2 alleles blend for a new phenotype
  • A homozygous red flower (RR) crosses with a
    homozygous white flower (WW), to make a Pink
    flower (RW)

16
  • Ex Japanese Four oclocks
  • RR red WW white RW pink
  • F1 F2

R W
R R
R W
W W
RW
RW
RR
RW
RW
RW
RW
WW
All Pink
1 red 2 pinks 1 white
17
Codominance p76
  • When both alleles are expressed in a cross.
  • Ex. A chicken with black feathers (BB) crosses
    with a chicken with white feathers(WW) to make
    offspring with black and white checkered
    feathers.
  • Ex.Different blood types in humans A, B, AB, O

18
  • Ex Red Coat - RR
  • White Coat WW
  • White Red Mixed RW (roan)

F1 R R
F2 R W
RW
RW
RW
R W
RR
W W
RW
RW
RW
WW
All Roan both red and white hair
1 red 2 roan 1 white
19
Codominance in humans p76
  • Disorder Sickle-Cell Anemia
  • Facts sickle-shaped blood cells block/clot up
    blood vessels point mutation
  • Symptoms pain in joints, anemia, weakness
  • Incidence 1 in 375 African Americans
  • Treatments bone marrow transplants, medicines

20
Dominance Cartoons p75
  • Draw a cartoon that shows what Codominance is.
    (half page)
  • Draw a cartoon that shows what incomplete
    dominance is.

21
Meiosis p78
  • Warm up What happens to cells during interphase
    mitosis?
  • The production of sex cells (egg sperm, aka
    gametes) through a series of 2 cell divisions.
    video
  • Each gamete ends up with half its genetic
    material in the end-haploid (23 chromosomes)
  • After fertilization, the embryo (baby) gets its
    full 46 chromosomes- diploid (or 23 pair)

22
http//www.palaeos.com/
23
Meiosis I
  • Interphase genetic material is duplicated
  • (fill in on right page- Meiosis I)
  • First Phase meiosis (46 pair) (p267)
  • Prophase 1 The 2 sets of chromosomes condense.
    Crossing over can occur.
  • Metaphase 1 chromosome pairs align at the
    center.
  • Anaphase 1 pairs separate
  • Telophase 1 Two daughter cells are formed each
    containing 23 pair of Chromosomes (diploid)

24
Crossing Over (Recombination) p78
  • Where a section of one chromosome switches places
    with the same section of another chromosome
  • This causes variation of genes.

25
http//www.accessexcellence.org
26
Meiosis- Phase 2 (fill in right)
  • Gamete formation
  • Prophase 2 DNA does not replicate.
  • Metaphase 2 Chromosomes of each daughter cell
    align in the centers
  • Anaphase 2 Chromosomes divide and migrate
    separately to each pole.
  • Telophase 2 Cell division is complete. Four
    gametes are obtained, each having only 23
    chromosome (haploid)
  • One parent cell produces 2 diploid daughter cells
    and then 4 haploid sex cells.

27
Animation
  • http//www.johnkyrk.com/meiosis.html

28
Draw label fig 10.12, p273 on left page under
this diagram
29
http//post.queensu.ca/
30
Animation
  • http//www.csuchico.edu/jbell/Biol207/animations/
    meiosis.html

31
Sex Determination p80
  • Warm up How is the gender of a baby determined?
  • The 23rd pair of chromosomes are XX for a female
    and XY for a male.
  • Mom can only pass on her X chromosome, but dad
    can pass X or Y.
  • Dad determines if offspring is male or female.
  • Dads give their Y to sons, Moms always give their
    X to their sons
  • Sex linked traits-traits on this pair of
    chromosomes, and can be traced back to a mother
    or father.

32
Sex-linked Disorders p80most disorders are
x-linked, recessive
  • Disorder Muscular Dystrophy (MD)
  • Facts recessive, x-linked many types of MD
  • Symptoms muscle loss weakness
  • Incidence mainly in males all ethnic groups
    have an equal chance of MD
  • Treatments physical therapy , braces, wheelchair

33
Sex-linked Disordersp80
  • Disorder Hemophilia
  • Facts recessive, x-linked blood does not have
    clotting factors
  • Symptoms bleed excessively or to death
  • Incidence mainly in males Royal Family
  • Treatments inject themselves with purified
    clotting factors to prevent or stop bleeding

34
Sex-linked Disorders p80
  • Disorder Color-blindness
  • Facts recessive, x-linked disorder Cones in
    eyes(color receptors) are absent or lack of
    pigment
  • Symptoms cannot tell difference between certain
    colors
  • Incidence mainly in males- passed from mother
  • red-green color blindness most common
  • Seeing only black/white is rare
  • Treatments none

35
A Difficult Decision p79
  • If one day, you and your future husband or wife
    were a carrier for a sex linked disorder, would
    you still have children? Back up your decision
    using examples from todays or previous notes.

36
Nondisjunction p82 video
  • Warm up how many chromosomes do we have?
  • when a chromosome pair fails to separate during
    meiosis-can happen to any chromosome pair
  • 2 types
  • 1.Monosomy when gamete has one less chromosome
    than it should
  • only 45 chromosomes
  • (need 46)
  • Ex Turner syndrome-
  • occurs only in females

37
Nondisjunction p82
  • 2.Trisomy when gamete has one more chromosome
    than it should
  • 47 chromosomes( need 46)
  • Ex Downs syndrome, extra 21 video

38
Questions p81
  • Q. How can a nondisjunction occur? (1/3 page)
  • Q. What is the difference between monosomy and
    trisomy? (1/3 page)
  • Read p 273 about polyploidy and answer question
    about the banana plant under figure 10.17
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