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CHAPTER%207%20EXTENDING%20MENDELIAN%20GENETICS

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CHAPTER 7 EXTENDING MENDELIAN GENETICS SECTION 1 CHROMOSOMES AND PHENOTYPES Two copies of each autosomal gene affect phenotype. One copy comes from the Father, the ... – PowerPoint PPT presentation

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Title: CHAPTER%207%20EXTENDING%20MENDELIAN%20GENETICS


1
CHAPTER 7 EXTENDING MENDELIAN GENETICS
2
SECTION 1 CHROMOSOMES AND PHENOTYPES
  • Two copies of each autosomal gene affect
    phenotype.
  • One copy comes from the Father, the other from
    the mother
  • ? What cellular process forms gamete cells?
    (aka haploid cells?)
  • Some disorders are caused by recessive alleles.
  • The Heterozygous form of these conditions are
    known as CARRIERS because they do not portray the
    disease, but can pass it on to the next
    generation.

3
DISORDERS CAUSED BY ALLELE COMBINATIONS
  • Recessive
  • ex. Sickle Cell Anemia
  • Dominant
  • ex. Huntingtons disease
  • Homozygous recessive to have the disease/disorder
  • The Heterozygous form of these conditions are
    known as CARRIERS because they do not portray the
    disease, but can pass it on to the next
    generation.
  • less common than recessive disorders.
  • Since caused by a dominant allele, there is a 50
    chance of the next generation having the disease.

4
SEX LINKED TRAITS
  • Sex chromosomes the X and Y
  • Females XX, Males XY
  • In X-linked traits
  • women can be carriers, normal, or affected
  • males are either affected or not since they have
    only 1 X
  • In Y-Linked traits
  • Only seen in males, and all the males in a family
    will be affected from father to son.
  • The X chromosome is SUPER HUGE as compared to
    the Y chromosome and must be present in either
    sex.

5
X CHROMOSOME INACTIVATION
  • X chromosome is HUGE, and in cats controls color.
  • The cells randomly turns one of the Xs off
    allowing one color to show through.
  • The Turned off X is called a BARR BODY.
  • This is how you get calico cats! ?

6
PATTERNS OF INHERITANCE REVIEW
  • Incomplete dominance-
  • occurs when neither of the dominant nor the
    recessive allele is masked during the
    heterozygous stage.
  • The phenotypes seem to BLEND
  • Codominance-
  • both alleles of a gene are expressed completely,
    neither is dominant or recessive.
  • Polygenic traits- ex skin color, eye color,etc
  • phenotype that is controled by two or more genes.
  • Epistasis occures when there is one gene that can
    mask/ interfere with ALL the rest. Example
    Albinism

7
POP QUIZ
  • What term do we use when there is a blending of
    phenotypes due to the heterozygous genotype? ex
    white, pink, Red
  • INCOMPLETE DOMINANCE
  • What term is used to describe the state where
    BOTH alleles are expressed completely, where
    neither is dominant or recessive?
  • CODOMINANCE
  • What term is used to describe a trait that is
    controlled by two or more genes?
  • POLYGENIC TRAIT

8
POP QUIZ
  • 4. What do we call the polygenic gene that can
    mask all the rest?
  • Epistatic gene
  • 5. What is the term used to describe the X
    chromosome that has been turned off in female
    cells?
  • Barr Body
  • 6. Why are dominant trait disorders less common
    in a population than recessive trait disorders?
  • Dominant trait disorders generally cause server
    damage and death for the creature, generally
    before it can pass on its genetic information

9
POP QUIZ BONUS
  • Sunlight can cause a persons hair to become
    lighter in color. Is this an example of an
    interaction between genes and the environment?
    Why or why not?
  • YES! because phenotype is altered by environment
  • Give an example of a trait that is considered to
    be polygenic.
  • Eye color, skin color, etc

10
HOME WORK
  • Read Chapter 7 sections 3 4 pages 209 217
  • Screen notes assignment Part one
  • Fold your 2 pieces of notebook paper so that each
    side has 6 boxes.
  • Everytime you come to a BOLD BLUE or BLACK
    paragraph heading you will do the following.
  • In the LEFT BOX you will write the page number
    and notes to sum up that section.
  • minimum of 12-15 words!
  • In the RIGHT box you will sketch a picture to
    illustrate what you wrote in the left box.
    Something to help you remember it.
  • You must have 8 box sets of words pictures.
  • Part two Investigation on page 219 s 1-4, must
    show work and use COMPLETE SENTENCES!!!

11
GENE LINKAGE ,MAPPING, PEDIGREES
  • chapter 7 sections 34

12
THOMAS HUNT MORGAN AND HIS FRUIT FLYS
  • Gene linkage was first studied by Morgan in fruit
    flies because they were easy to raise and had few
    characteristics to easily study.
  • He expected the Mendelian 9331 ratio but his
    results did not always follow that.
  • He observed that some of the triats seemed to be
    inherited together in four groups.
  • we later learned that they only had four
    chromosomes
  • He called these genes LINKED GENES because they
    were on the same chromosome, and found out that
    the CHROMOSOMES not the GENES assorted
    independently during meiosis.

13
  • He called these genes LINKED GENES because they
    were on the same chromosome, and found out that
    the CHROMOSOMES not the GENES assorted
    independently during meiosis.
  • He also concluded that chromosomes must exchange
    homologous genes during meiosis CROSSING OVER

14
LINKAGE MAPS
  • Are used to estimate distances between genes.
  • The CLOSER together two genes are, the MORE
    likely they will be inherited together.
  • The FARTHER apart two genes are, the LESS likely
    they will be inherited together.
  • On a linkage map, one map unit is equal to one
    cross-over for each 100 offspring, or one point.

15
MAP CHALLENGE USE THE DATA BELOW TO ANSWER THE
QUESTIONS
  • Gene A and B cross over 6.0 of the time.
  • Gene B and C cross over 12.5 of the time.
  • Gene A and C cross over 18.5 percent of the time.
  • Which two genes are closest together?
  • Which two genes are farthest apart?
  • Draw a map showing the location of each gene and
    its / map unit distance from the next.
  • ex. ______A__________B__C_________
  • 25 2
  • so A to C 27

16
PEDIGREES
  • Human genetics, or any mammals genetics follow a
    set of patterns that can be easily recorded in
    pedigrees.
  • A Pedigree is a chart that can help trace the
    phenotypes and genotypes in a family for a
    particular trait.
  • Autosomal traits are easily traced since the
    traits will follow a Mendelian punnett square.
  • Sex linked traits leave a distinct pattern that
    requires the observed to remember if the trait is
    dominant or recessive, X-linked or Y linked

17
  • squares male
  • circles females
  • Half filled means carrier
  • Filled means affected

I
A
II
B
III
C
Give the Genotypes for IA, IIB, and IIIC
18
KARYOTYPES
  • Are pictures of ALL the chromosomes in a cell.
  • Chemical stains produce a pattern of stains on
    the chromosomes to help identify them.
  • Karyotypes can be used to show whole or partial
    chromosome deletions or additions.
  • Ex. Downs syndrome is caused by an extra 21
    chromosome.

19
HOMEWORK
  • Complete the at home investigation on page 219.
    Answer ALL the Analyze and conclude questions.
    (1-4)
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