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Extending Mendelian Genetics Chapter 7
Complex Patterns of Inheritance Day One
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GENES are more complicated than Mendel thought
ENVIRONMENT influences ____________________________ the ________________________. = ________________________ Genes ________ the ______ for development, but how plan unfolds also _______ on ______________conditions. expression of genes “Nature versus Nurture” provide plan depends environmental
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GENES are more complicated than MENDEL thought
Traits determined by ____________have _____“___________” phenotypes. more than one gene many in-between
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Sex-linked Traits Traits (genes) located on the sex chromosomes
Mendelian Genetics 9/19/2018 Sex-linked Traits Traits (genes) located on the sex chromosomes Sex chromosomes are X and Y XX genotype for females XY genotype for males Many sex-linked traits carried on X chromosome copyright cmassengale
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Sex-linked Traits Example: Eye color in fruit flies Sex Chromosomes
Mendelian Genetics 9/19/2018 Sex-linked Traits Example: Eye color in fruit flies Sex Chromosomes XX chromosome - female XY chromosome - male fruit fly eye color copyright cmassengale
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Sex-linked Trait Problem
Mendelian Genetics Sex-linked Trait Problem 9/19/2018 Example: Eye color in fruit flies (red-eyed male) x (white-eyed female) XRY x XrXr Remember: the Y chromosome in males does not carry traits. RR = red eyed Rr = red eyed rr = white eyed XY = male XX = female XR Xr Y copyright cmassengale
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Sex-linked Trait Solution:
Mendelian Genetics 9/19/2018 Sex-linked Trait Solution: XR Xr Y 50% red eyed female 50% white eyed male XR Xr Xr Y copyright cmassengale
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Sex Linked Traits Most sex-linked traits on X chromosome are recessive
Examples include: hemophilia, red-green colorblindness, and a form of muscular dystrophy
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Colorblindess Test A person with red-green color blindness sees a number 2.
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Colorblindess Test
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Colorblindness Test
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Hemophilia In this pedigree, only males are affected, and sons do not share the phenotypes of their fathers. Thus, hemophilia is linked to a sex chromosome–the X. Expression of hemophilia often skips generations. Thus, it is recessive. Extensive bruising of the left forearm and hand in a patient with hemophilia. Hemophilia Hemophilia is a condition of excessive bleeding caused by missing clotting factors in the blood. Hemophiliacs are prone to bruising, as illustrated in the photo here, and to other, potentially fatal, risk factors. In this pedigree, there is a trend for only males to express the trait strongly suggesting the role of sex chromosomes. However, the sons do not share the phenotypes of their fathers, so the Y chromosome is not a likely candidate. Thus, we can conclude that the gene for hemophilia is on the X chromosome. Since the trait skips generations, we can assume that an allele for hemophilia is recessive to an allele for normal blood clotting factors. Although rare, a female can be afflicted if she inherits an allele for hemophilia on both X chromosomes. Reference Campbell, N. E. & Reece, J. B. (2002). Biology (6th ed.). San Francisco: Benjamin Cummings. Image Reference Young, M. (2005). Pedigree chart. Houston, TX: Baylor College of Medicine, Center For Educational Outreach. Hemophilia A. Retrieved from
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Genotypes for females XHXH = normal blood clotting, non-carrier
XHXh = normal blood clotting, carrier of gene XhXh = female with hemophilia Queen Victoria of the United Kingdom was a carrier of hemophilia
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Genotypes for Males XHY = normal blood clotting
XhY = male with hemophilia Tsarevich Alexei of Russia had hemophilia
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Cross a carrier mother with a normal father.
XH Xh Y
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No daughters with hemophilia, ½ of sons with hemophilia
XH Xh XHXH XHXh Y XHY XhY
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Cross a hemophiliac father with a normal (non-carrier) mother.
XH Xh Y
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All daughters are carriers, no sons have hemophilia.
XH Xh XHXh Y XHY
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Disorders Caused by Recessive Alleles
Two copies of the allele must be present for a person to have the disorder. Appear in offspring of parents who are both heterozygotes. Each parent has one dominant (normal) allele that masks the disease-causing allele. A person that is homozygous for the recessive allele has the disease. A person that is heterozygous for the allele will not have the disease, but will be a carrier. Carrier – does not show disease symptoms but can pass on the disease-causing allele.
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GENES are more complicated than MENDEL thought
KINDS OF DOMINANCE ____________________ COMPLETE DOMINANCE INCOMPLETE DOMINANCE CO-DOMINANCE
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COMPLETE DOMINANCE __________ allele _______ the ___________ one
Dominant __________ allele _______ the ___________ one PATTERN ? ____________ allele ________ in a _____ratio in the ____ generation masks recessive Recessive returns 3:1 F2
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INCOMPLETE DOMINANCE __________ expected _____ ratio in F2 generation
DON’T SEE __________ expected _____ ratio in F2 generation _____________ organisms with one dominant and one recessive allele show a _________ in-between trait 3:1 Heterozygous BLENDED
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Incomplete Dominance An individual displays a trait that is intermediate between the two parents Example: a red snapdragon crossed with a white snapdragon produces pink offspring
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Red = RR, White = WW, Pink = RW
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Make a Punnett square for a red plant crossed with a white plant
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All offspring are pink, with RW genotype
R R RW W
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What happens if you cross two pink snapdragons?
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Offspring are 1 red, 2 pink, and 1 white
R W RR RW WW R W
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1 red (RR), 2 pink (RW), 1 white (WW)
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Incomplete dominance in horse coat color
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Codominance Two dominant alleles are expressed at the same time
Roan coat color in horses or cows is an example A roan horse has both red and white hair
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Codominance red white roan
Defined: When both alleles are dominant and equally expressed The colors do NOT blend together, but are equally seen Ex: Cattle Coat Red cow x White cow = Roan Cow Ex: Human Blood types Type A x Type B = Type AB red white roan
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Roan has red and white hairs
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CO-DOMINANCE BOTH SAME TIME
_______ traits are expressed at ___________ (_____________________) in heterozygote NO BLENDING ROAN A ________HORSE has ______________ hair and __________ hair side by side BOTH RED WHITE
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Parents Codominance in chicken feather color. Black and White feathers Erminette
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Codominance Example In some chickens, the gene for feather color is controlled by codominance. The allele for black is CB and the allele for white is CW. The heterozygous phenotype is known as erminette. a. What is the genotype for black chickens? ____ b. What is the genotype for white chickens? ____ c. What is the genotype for erminette chickens ______? CBCB CWCW CBCW
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CoDominance Example If two erminette chickens were crossed, what is the probability that: a. They would have a black chick? ____% b. They would have a white chick? ____% Parents: ____ X ____
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Codominance example CB CW CB CW
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Codominance example CB CW CBCB CBCW CB CW CBCW CWCW
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CoDominance Example If two erminette chickens were crossed, what is the probability that: a. They would have a black chick? ____% b. They would have a white chick? ____% Parents: ____ X ____ 25 25 CBCW CBCW
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Practice problems: Using XBXB x XbY, answer the following questions (Show the Punnett square): What proportion/percent of the male children are colorblind? What proportion/percent of the female children are colorblind? In snapdragons, flower color is controlled by incomplete dominance. The two alleles are red (R) and (W). The heterozygous genotype is expressed as pink. What is the phenotype of a plant with the genotype of RR? What is the phenotype of a plant with the genotype WW? What is the phenotype of a plant with the genotype RW?
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Extending Mendelian Genetics Chapter 7
Complex Patterns of Inheritance Day Two
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GENES are more complicated than Mendel thought
Some traits have ____________ allele __________ = ____________________ EX: blood type Allele choices ___ ___ ___ MORE than 2 choices MULTIPLE ALLELE TRAIT A B O
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An A allele tells the cell to put “A” glycoproteins on its surface
BLOOD TYPES An A allele tells the cell to put “A” glycoproteins on its surface
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different “B” glycoprotein on its surface
BLOOD TYPES A B allele tells the cell to put a different “B” glycoprotein on its surface
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the cell NOT to put anything on the surface
BLOOD TYPES An O allele tells the cell NOT to put anything on the surface
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A and B are CO-DOMINANT A cell with BOTH an A and a B allele has BOTH “A” and “B” glycoproteins on its surface
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Blood types are also an example of codominance.
The ABO blood types result from codominant alleles This blood group consists of 3 different alleles Dominant A allele Dominant B allele Recessive O allele A and B are equally dominant
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PHENOTYPE (BLOOD TYPE)
BLOOD TYPES & ALLELES GENOTYPE PHENOTYPE (BLOOD TYPE) IAIA IAi IBIB IBi ii IAIB A A B B O AB
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O ____ can donate to EVERY BLOOD TYPE = _________________
DONOR BLOOD O ____ can donate to EVERY BLOOD TYPE = _________________ Nothing on surface to recognize as “NOT SELF” UNIVERSAL DONOR YOU DON’T HAVE ANYTHING I DON’T HAVE! Body images modified from:
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AB can only GIVE to AB BUT . . .
______ can RECEIVE FROM EVERY BLOOD TYPE = ____________________ AB UNIVERSAL RECIPIENT
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List the genotypes. 4 IAIB List the phenotypes. 4 type AB blood
Ex: Cross Jason who is homozygous for type A blood with Maria who is homozygous for type B blood. List the genotypes. 4 IAIB List the phenotypes. 4 type AB blood IA IA IB IAIB IAIB IB IAIB IAIB
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Ex: Cross Mike who is heterozygous for type A blood with Lisa who is heterozygous for type B blood.
List the genotypes. 1 IAIB, 1IAi, 1IBi, 1 ii List the phenotypes. 1 type AB blood 1 type A blood 1 type B blood 1 type O blood Probability of Heterozygous individual? 75% IA i IBi IB IAIB i IAi ii
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V. Polygenic traits Traits that are influenced by 2 or more genes
Examples include human height,weight,hair color, eye color, and skin color
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Epistasis One gene that interferes with the expression of other genes.
Example is with albinism. One gene interferes with all other genes for pigment production.
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The environment interacts with genotype.
Phenotype is a combination of genotype and environment. The sex of sea turtles depends on both genes and the environment Height is an example of a phenotype strongly affected by the environment.
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A pedigree is a chart for tracing genes in a family.
Phenotypes are used to infer genotypes on a pedigree. Autosomal genes show different patterns on a pedigree than sex-linked genes.
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A circle represents a female A square represents a male
On a pedigree: A circle represents a female A square represents a male A horizontal line connecting a male and female represents a marriage A vertical line and a bracket connect the parents to their children A circle/square that is shaded means the person HAS the trait. A circle/square that is not shaded means the person does NOT have the trait. Children are placed from oldest to youngest. A key is given to explain what the trait is.
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Marriage Male-DAD Female-MOM Has the trait Female-daughter Male- Son Male-Son Oldest to youngest
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ff Ff Ff Key: affected male affected female
Steps: Identify all people who have the trait. For the purpose of this class all traits will be given to you. In this example, all those who have the trait are homozygous recessive. Can you correctly identify all genotypes of this family? F- Normal f- cystic fibrosis Ff Key: affected male affected female unaffected male unaffected female
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Several methods help map human chromosomes.
A karyotype is a picture of all chromosomes in a cell. X Y
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Karyotypes can show changes in chromosomes.
deletion of part of a chromosome or loss of a chromosome large changes in chromosomes extra chromosomes or duplication of part of a chromosome
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Practice problems A man with type A blood marries a woman with type A blood. They have the first child with blood type O. What are the genotypes of the father, mother, and baby? You are blood type O and you marry a person with blood type AB. Complete the Punnett square for this cross. List the possible blood types (phenotypes) of your offspring.
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