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Bio 178 Lecture 25 Genetics. Reading Chapter 13 Quiz Material Questions on P 276-278 Chapter 13 Quizzes on Text Website (www.mhhe.com/raven7)

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Presentation on theme: "Bio 178 Lecture 25 Genetics. Reading Chapter 13 Quiz Material Questions on P 276-278 Chapter 13 Quizzes on Text Website (www.mhhe.com/raven7)"— Presentation transcript:

1 Bio 178 Lecture 25 Genetics

2 Reading Chapter 13 Quiz Material Questions on P 276-278 Chapter 13 Quizzes on Text Website (www.mhhe.com/raven7)

3 Outline Genetics Non-Mendelian Patterns of Inheritance Human Genetics

4 Non-Mendelian patterns of Inheritance (cntd.) Incomplete Dominance When 2 alleles produce heterozygotes that are phenotypically different from either parent. The heterozygotes have a phenotype that is intermediate between the phenotypes of the parents. Example - Japanese four o’clocks Explanation: The unmasked Mendelian genotypic ratio is a result of the heterozygotes having less red pigment than the red homozygotes.

5 Incomplete Dominance

6 Japanese Four O’clocks http://www.bio.miami.edu/dana/250/mirabilis.jpg

7 Incomplete Dominance - Snapdragon  J. Elson-Riggins

8 Non-Mendelian patterns of Inheritance (cntd.) Environmental Effects When the degree of expression of allele is affected by the environment. Example - Temperature Sensitive Alleles The ch allele in Himalayan rabbits and Siamese cats encodes an enzyme that controls melanin production. Effect of Temperature: Temps >33  C - Enzyme inactive (no melanin  white) Temps < 33  C - Enzyme active (melanin  brown)

9 Himalayan Rabbit http://www.bio.miami.edu/dana/250/himalayanbun.jpg

10 Arctic Fox

11 Non-Mendelian patterns of Inheritance (cntd.) Multiple Alleles and Codominance Often there are multiple alleles for a trait. When no single allele is dominant, the alleles are codominant. Example - ABO Blood group The gene I codes for an enzyme that puts sugars on red blood cells (rbcs). The sugars are important for self-recognition by the immune system. Alleles: I = Sugar on (I A  galactosamine, I B  galactose) i = Gene non-functional

12 ABO Blood Group Genotypes & Phenotypes

13 ABO Blood Groups (Cntd.) Immune Response The immune system will reject rbcs coated with a sugar it does not recognize as self, as it has antibodies to non-self. Recipient/ Donor ABABO A B O

14 ABO Blood Groups (Cntd.) Immune Response The immune system will reject rbcs coated with a sugar it does not recognize as self as it has antibodies to non-self. Recipient/ Donor ABABO A+--+ B-+-+ ++++ O---+

15 Codominance Example - Roan Horse http://www.bio.miami.edu/dana/250/roanhorse.html

16 Non-Mendelian patterns of Inheritance (cntd.) Multiple Alleles (Cntd.) Example - Rhesus Blood group Usually treated as a 2 allele system, but there are 8 alleles for this trait (Rh factor). Rh codes for a surface protein on rbcs. Rh + = Has Rhesus factorRh - = No Rhesus factor Rh + is dominant to Rh - In contrast to ABO, Rh - individuals do not have antibodies to Rh unless they have been previously exposed. Eg. Erythroblastosis fetalis (hemolytic disease of newborns)

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18 Human Genetic Disorders Hemophilia Sickle Cell Anemia Huntington’s Disease

19 Genetic Disorders Frequency Although genetic disorders are rare: (a) Their frequencies may be higher in particular populations. (b) Natural selection does not entirely remove them from a population. Dominance Mostly, but not all, are recessive.

20 Studying Patterns of Inheritance Pedigrees Family trees documenting the inheritance of a trait. Example - Hemophilia Clotting disorders caused by a mutation resulting in a loss of function in any one of the 12 clotting factors (proteins) involved in the clotting cascade. Sex-Linked hemophilia A recessively inherited hemophilia that is carried on the X chromosome.  Any male with the recessive allele (X h Y) will have the disease. Any heteozygous female will be a carrier.

21 Royal Hemophilia The hemophilia mutation occurred either in Queen Victoria or her parents and therefore entered the royal line.

22 Royal Hemophilia http://www.people.virginia.edu/~rjh9u/roylhema.html

23 Single Base Substitution - Sickle Cell Anemia The Disease Defective hemoglobin that is unable to carry O 2 properly. Hemoglobin molecules stick to each other under low O 2 conditions  sickle cell crisis.

24 Sickle Cell Anemia (Cntd.) Inheritance Homozygous recessive. Cause Mutation in 1 base of the gene encoding  -hemoglobin: Mutation: GAG  GTG AA: Glutamic acid (polar)  Valine (non-polar) Results in a “sticky patch” (hydrophobic interaction). Why does this deleterious allele persist? Common in blacks. Confers resistance to falciparum malaria - heterozygotes have a survival advantage in areas where Plasmodium falciparum is endemic  NATURAL SELECTION.

25 Sickle Cell Anemia

26 Plasmodium falciparun  E.G. Platzer http://www.sb-roscoff.fr/CyCell/Page45.htm


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