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Rules of probability

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Title: Rules of probability


1
Chapter 14 Highlights
  • Rules of probability
  • 1. Rule of multiplication
  • a. how do we determine the chance that two
    or more independent events will occur
    together in a specific combination?
  • b. compute probability for each event then
    multiply independent probabililities to
    obtain the overall probability
  • 2. Rule of addition
  • a. a. used to find the probabilility of an
    event that can occur in two or more
    different ways is the sum of the
    separate probabilities of those ways

2
Example TtRr X TtRr
  • The probability of getting a tall offspring is ¾.
  • The probability of getting a red offspring is ¾.
  • The probability of getting a tall red offspring
    is ¾ x ¾ 9/16

3
Comment
  • Use the Product Rule to calculate the results of
    complex crosses rather than work out the Punnett
    Squares.
  • Ex TtrrGG X TtRrgg
  • What is the probability that you would get a Tall
    plant with Wrinkled (dom) Green seeds?

4
Solution
  • What is the probability that you would get a Tall
    plant with Wrinkled (dom) Green seeds?
  • Ts Tt X Tt
  • Rs rr X Rr
  • Gs GG x gg
  • Product is

5
3. Rules can be combined a. Trihybrid cross
PpYyRr x Ppyyrr What is the probability
that offspring will exhibit recessive
phenotypes for at least two of the 3 traits?
Possibilities ppyyRr, ppYyrr, Ppyyrr,
PPyyrr, ppyyrr,
6
B. Extending Mendelian Genetics 1. Incomplete
Dominance 2. Codominance 3. Multiple
alleles 4. Pleiotropy pleion (Greek for
more) a. one gene affecting many
phenotypes 5. Epistasis (Greek for standing
upon) a. a gene at one locus alters
phenotype of a gene at a second locus b.
Mice coat color and pigment deposit (color) or
not (albino) 6. Polygenic Inheritance a. an
additive effect of 2 or more genes on a single
phenotypic trait (converse to
pleiotropy) b. skin pigmentation (3
separately inherited genes)
7
(No Transcript)
8
Comment
  • Rh blood factor is a separate factor from the ABO
    blood group.
  • Rh dominant
  • Rh- recessive
  • A blood dihybrid trait

9
Skin Pigmentation Polygenic Inheritance Quantitati
ve character
10
Summary for chapter 14
  • Know the Mendelian crosses and their patterns.
  • Be able to work simple genetic problems
    (practice).
  • Watch genetic vocabulary.
  • Be able to read pedigree charts.
  • Understand carriers and be able to work
    problems with these.
  • Know Huntington disease and sickle cell

11
Chapter 15 Highlights
  • Sex linked traits
  • Duchenne Muscular dystrophy
  • Hemophilia
  • Color blindness
  • Seen more in maleswhy?

12
X inactivation in Females
  • One of the X chromosomes is inactivated in each
    cell of a female during embryonic development.
  • Inactive X is condensed and called a Barr
    bodylies along the inside of the nuclear
    envelope.
  • Occurs randomly and independently (females
    consist of a mosaic of 2 types of cells)
  • Example Tortoiseshell cat and Calico cats
  • How is the X chromosome inactivated
  • Modification of the DNA (attachment of a methyl
    group to nucleotides) chapter 18
  • XIST gene

13
Mapping the distance btw genes using
recombination data
  • Recombination frequencies depend on the distance
    between genes on a chromosome
  • Can create a linkage map from this data
  • Distances btw genes are map units
  • A map unit is 1 of recombination frequency
  • Genes are linked if they are on the same
    chromosome

14
Page 293
How you tell if genes are linked
15
A Test Cross to determine linkage and if linkage,
what is the percentage of recombination so you
can map the genes.
16
They dont look like the parents
17
Mutations of Chromosomes
1. Abnormal of Chromosomes
Nondisjunction a. members of a chromosome pair
fail to separate b. Meiosis I c. Meiosis II d.
Monosomic vs. Trisomic e. Abnormal of sex
chromosomes (aneuploidy) f.
polyploidy (triploidy 3n or tetraploidy 4n)
2. Alterations in chromosome structure a.
Deletion b. Duplication
c. Inversion d. Translocation
18
Nondisjunction
19
Alterations in Chromosomes
  • Know the following disorders and causes for the
    disorders
  • down syndrome
  • Klinefelter syndrome
  • Turner syndrome
  • cri du chat

20
Genomic Imprinting
  • The differential expression of genetic material
    depending on whether it is inherited from the
    male or female parent
  • Occurs during meiosis and results in the
    silencing of one allele of certain genes.
  • Example mouse gene Igf2only the paternal gene
    is expressed (it had methyl groups attached to
    cytosine nucleotides) exception to the rule that
    methylated DNA is silenced (not expressed)
  • Most imprinted genes are critical for embryonic
    development. (mouse experiment)normal
    development requires embryonic cells have exactly
    one copy of certain genes.

21
Organelle genes
  • Cytoplasmic genes genes outside of the nucleus
  • Mitochondria, chloroplasts, other plant plastids
  • Contain small circular piece of DNA
  • Distributed to offspring from the maternal parent
    (egg)
  • Mitochondrial diseases (Myopathy, Lebers
    hereditary optic neuropathy)
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