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    Mendelian Inheritance

    Part 1

    Prepared By: Asst. Prof.Sheryl Santa Cruz- Biscocho

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    Gregor Mendel

    1823-1884

    Father of

    Genetics

    Monk in Austria

    Experimented

    with garden peas

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    Short

    Tall

    Tall

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    Mendels Hypotheses

    Each parent has two factors (alleles)

    Each parent gives one of those factors to the

    offspring Tall has TT

    Short has tt

    Tall is DOMINANT Short is recessive

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    TT tt

    T t

    Tt

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    TT TT

    T T

    TT

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    tt tt

    t ttt

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    Law of Segregation

    Alleles separate during gamete production

    Gametes have one allele for each trait

    During fertilization gametes combine at

    random to form individuals of the next

    generation

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    Discovery of Chromosomes in 1900

    Confirmed Law of Segregation Chromosomes

    are in pairs

    Each chromosome hasone of the allele pair

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    Chromosomes line up in a

    double row.

    Meiosis Metaphase

    Assume a T allele on each red chromatid and a t

    allele on each blue chromatid

    T T t t

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    Chromosomes separate

    Each each daughter cell getsdoubled chromosomes

    T Tt t

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    Doubled Chromosomes Separate

    in Second Meiotic Division

    T T t t

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    Each gamete will have a T allele or a t

    allele

    T T t t

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    Allele

    Member of a paired gene

    One allele comes from each parent

    Represented by a single letter

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    Dominant & Recessive

    Alleles Dominant alleles are expressed

    Recessive alleles are not expressed in the

    presence of a dominant allele

    Recessive alleles are only expressed if both

    recessive alleles are present

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    Gene

    A unit of heredity that controls the

    development of one trait

    Made of DNA

    Most genes are composed of two alleles

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    Homozygous

    Both alleles alike

    AA or aa

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    Heterozygous

    Alleles are different

    Aa

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    Genotype

    Genetic make up

    Represented by alleles

    TT & Tt are genotypes for TALL pea plants

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    Phenotype

    A trait

    Genotype determines the phenotype

    Tall is a phenotype

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    Homologous Chromosomes

    Chromosomes of the same pair

    Each homologue will have one allele for a

    paired gene

    Homologous chromosomes pair up during

    meiosis

    Only one of each homologue will be in each

    gamete

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    Sickle Cell Anemia

    RBCs sickle shaped

    Anemia

    Pain

    Stroke

    Leg ulcers

    Jaundice

    Gall stones

    Spleen, kidney & lungs

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    Sickle Cell Anemia

    Recessive allele s, codes for hemoglobin S

    Long rod-like molecules

    Stretches RBC into sickle shape

    Homozygous recessive ss, have sickle cell

    anemia

    Heterozygous Ss, are carriers

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    Albinism

    Lack of pigment

    Skin

    Hair Eyes

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    Amino Acids Melanin PigmentEnzyme

    A a

    AA = Normal

    pigmentation

    Aa = Normalpigmentation

    aa = Albino

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    PKU Disease

    Phenylalanine excess

    Mental retardation if

    untreated

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    Phenylalanine TyrosineEnzyme

    P p

    PP = Normal

    Pp = Normal

    pp = PKU

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    If a man & woman are both carriers

    (heterozygous) for albinism. What is

    the chance their children will inherit

    albinism? Solve using punnet square

    use letter a.

    Monohybrid Cross or One Trait

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    AA = Normal

    pigmentation

    Aa = Normalpigmentation

    (carrier)

    aa = Albino

    Man = Aa Woman = Aa

    A

    a a

    A

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    A

    a

    a

    A AA

    Aa

    Aa

    aa

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    AA

    Aa

    Aa

    aa

    Genotypes

    1 AA, 2Aa, 1aa

    Phenotypes

    3 Normal

    1 Albino

    Probability

    25% for albinism

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    If a man & woman are both

    carriers (heterozygous) for PKU

    disease. What is the chance their

    children will inherit PKU disease?

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    p

    p

    P PP

    Pp

    Pp

    pp

    P

    PP = Normal

    Pp = Normal

    (carrier)

    pp = PKU disease

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    PP

    Pp

    Pp

    pp

    Genotypes

    1 PP, 2Pp, 1pp

    Phenotypes

    3 Normal

    1 PKU disease

    Probability

    25% for PKU disease

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    If a man with sickle cell anemia

    marries a woman who is a carrier.

    What is the chance their children

    will inherit sickle cell anemia?

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    s

    s

    s Ss

    Ss

    ss

    ss

    S

    SS = Normal

    Ss = Normal

    (carrier)

    ss = Sickle Cell

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    Ss

    Ss

    ss

    ss

    Genotypes

    2 Ss, 2ss

    Phenotypes

    2 Normal (carriers)

    2 Sickle cell

    Probability

    50% for Sickle cell

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    Dwarfism = D

    Normal height = d

    DD = Dwarfism

    Dd = Dwarfism

    dd = Normal height

    Dwarfism

    Dwarf Band

    http://www.quigsmss.com/kingzhomepage.htmhttp://www.quigsmss.com/kingzhomepage.htm
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    A man with heterozygous

    dwarfism marries a woman who

    has normal height. What is thechance their children will inherit

    dwarfism? Dwarfism is dominant.

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    d

    d

    D Dd

    dd

    Dd

    dd

    d

    DD = Dwarf

    Dd = Dwarf

    dd = Normal

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    Dd

    dd

    Dd

    dd

    Genotypes

    2 Dd, 2dd

    Phenotypes

    2 Normal

    2 Dwarfs

    Probability

    50% for Dwarfism

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    Law of Independent Assortment

    The inheritance of one gene does not

    influence the inheritance of another gene if

    they are on separate chromosomes. The gene for albinism does not affect the

    gene for dwarfism

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    Dihybrid Cross or Two Traits

    A heterozygous tall plant that is also

    heterozygous for yellow seeds is crossed

    with another plant with the same genotype Tall and yellow seeds are dominant to short

    and green seeds.

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    Tall Yellow

    TtYy

    TY

    What gametes can each parent produce?

    Ty

    tYty

    TtYy

    TY

    Ty

    tYty

    Tall Yellow

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    9 Tall-Yellow

    Match gametes on a Punnent Square

    TY

    Ty

    tY

    ty

    TY Ty tY ty

    TtYy

    TtYy

    TTYY TTYy TtYY

    TTYy TTyy Ttyy

    TtYY TtYy ttYY ttYy

    TtYy Ttyy ttYy ttyy

    3 Tall-Green

    3 Short-Yellow

    1 Short-Green

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    A man with blue eyes and normalheight marries a woman with

    heterozygous brown eyes and

    heterozygous dwarfism. What arethe possible phenotypes of their

    children? Dwarfism & brown eyes

    are dominant.

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    Normal height-Blue

    ddbb

    db

    What gametes can each parent produce?

    DdBb

    DB

    Db

    dBdb

    Dwarf-Brown

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    DB

    Db

    dB

    db

    Match gametes on Punnent Square

    db

    DdBb

    Ddbb

    ddBb

    ddbb

    Dwarf-Brown eyes

    Dwarf-blue eyes

    Normal height-Brown eyes

    Normal height-Blue eyes

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    X-linked Traits

    Alleles on the X chromosome

    Women have two alleles

    Men have one allele

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    Hemophilia

    Blood clotting impaired

    Recessive allele, h

    carried on X cmsX-linked recessive trait

    More common in males

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    XH XH = Normal Female

    XH Xh = Normal Female

    (Carrier)

    Xh Xh = Hemophiliac Female

    XH

    y = Normal MaleXhy = Hemophiliac Male

    Alleles must be written on X

    chromosome

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    A man with hemophilia marries a

    normal woman who is not a

    carrier. What is the chance theirchildren will inherit hemophilia?

    Hemophilia is X-linked recessive.

    XH XH = Normal Female

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    y

    XH

    Xh XH Xh

    XH

    XH Xh = Normal Female

    (Carrier)

    Xh Xh = Hemophiliac Female

    XHy = Normal Male

    Xhy = Hemophiliac Male

    XH Xh

    XHy XHy

    X

    XH

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    Genotypes

    2 XH Xh, 2XHy

    Phenotypes

    2 Carrier Females

    2 Normal Males

    Probability

    O% for Hemophilia

    y

    H

    Xh XH Xh XH Xh

    XHy XHy

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    A normal man marries a normal

    woman who is a carrier for

    hemophilia. What is the chancetheir children will inherit

    hemophilia?

    XH XH = Normal Female

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    y

    Xh

    XH

    XH

    XH Xh = Normal Female

    (Carrier)

    Xh Xh = Hemophiliac Female

    XHy = Normal Male

    Xhy = Hemophiliac Male

    XH XH XH Xh

    XHy Xhy

    XhXH

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    Genotypes

    1XH XH, 1XH Xh,

    1XHy, 1 Xhy

    Phenotypes

    2 Normal Females

    1 Normal Males

    1 Male Hemophiliac

    Probability50% for Male Hemophiliac

    0% for Female Hemophiliac

    y

    XH XH XH XH Xh

    XHy

    X

    h

    y

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    Hypertrichosis

    X-linked dominant

    Similar gene in apes