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AP Biology Exam Review Put Your Knowledge to the Test

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Presentation on theme: "AP Biology Exam Review Put Your Knowledge to the Test"— Presentation transcript:

1 AP Biology Exam Review Put Your Knowledge to the Test
Enter the Game How to play

2 How This Works Read the Question
Click on the button of the right answer If you are wrong you go back to the start, if you answer correctly, you move on. **Click on the buttons only, not the page*** Enter the Game

3 Genetics 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24

4 Genetics Continued 25 26 27 28 29 35 30 31 32 33 34

5 A B C 1. What are Mendel’s Laws? Law of Segregation
Law of Independent assortment C Both Law of Segregation and Law of Independent Assortment

6 Nope! Try Again BACK TO QUESTION

7 Right!!!!!!!! Both the Law of Segregation and the Law of Independent Assortment are included in Mendel’s Law The Law of Segregation states that each allele segregates separately. One of each homologous chromosomes goes to each new cell. The Law of Independent Assortment states that in a dihybrid cross, each trait is independent of the other. BACK TO GENETICS PAGE

8 A B C 2. What is a Locus? The copied strand of the chromosome.
Exact location on a chromosome where a gene is located. C The offspring generation

9 Wrong! Try Again BACK TO QUESTION

10 Right!!!!!!!! A locus is the exact location on a chromosome where a gene is located BACK TO GENETICS PAGE

11 A B C 3. What is progeny? The offspring generation
The parent generation C A sex influenced trait

12 SORRY, Try again! BACK TO QUESTION

13 Progeny is the offspring generation of a test cross
RIGHT! Progeny is the offspring generation of a test cross BACK TO GENETICS PAGE

14 4. What is a homologous pair?
Every cell contains two copies of each chromosome B The chromosome and its copy C The original pair of chromosomes

15 Wrong Answer! BACK TO QUESTION

16 ***RIGHT*** In a homologous pair, every cell contains two copies of each chromosome BACK TO GENETICS PAGE

17 5. Define an x-inactivation
A genetic defect on the x chromosome B The x chromosome replicates uncontrollable C One of the x chromosomes does not uncoil into chromatin, it becomes a barr body instead.

18 TRY AGAIN BACK TO QUESTION

19 CORRECT X-inactivation is when one of the x chromosomes does not uncoil into chromatin and becomes a barr body instead BACK TO GENETICS PAGE

20 6. What is a test cross? A A cross between any two pair of alleles to find the progeny When you are trying to figure out what the make up of the allele is, A_ (either A or a), and you cross it with a pure recessive allele B C A test between progeny to find the parent generation

21 Sorry, try again BACK TO QUESTION

22 Yeah!! A test cross is when you are trying to figure out what the make up of the allele is, A_ (either A or a), and you cross it with a pure recessive allele BACK TO GENETICS PAGE

23 7. In the genus Homo sapien, who is the heterogametic sex?
Female B Either sex could be the heterogametic sex C Male

24 WRONG! BACK TO QUESTION

25 ~RIGHT~ In the genus Homo sapien, the male is the heterogametic sex
BACK TO GENETICS PAGE

26 8. In the genus Homo sapien, who is the homogametic sex?
Female B Male C Either sex could be the homogametic sex

27 NOPE, TRY AGAIN! BACK TO QUESTION

28 ALRIGHT! In the genus Homo sapien, the female is the homogametic sex
BACK TO GENETICS PAGE

29 9. What is the genotype of the blood type A?
AA and AB B AB and AO C AA and AO

30 Sorry, wrong answer BACK TO QUESTION

31 RIGHT!! The genotype of blood type A is AA or AO BACK TO GENETICS PAGE

32 10. What is the genotype of the blood type B?
BB and BO B BB and AB C AB and BO

33 WRONG BACK TO QUESTION

34 YEP! The genotype for blood type B is BO or BB BACK TO GENETICS PAGE

35 11. What is the genotype of the blood type AB?
AB and AO B AB C AA and AB

36 ~TRY AGAIN~ BACK TO QUESTION

37 ***RIGHT*** The genotype for blood type AB is AB BACK TO GENETICS PAGE

38 12. What is the genotype of the blood type O?
OO and BO B OO C AO and OO

39 Try Again! BACK TO QUESTION

40 CORRECT!!!! The Genotype for blood type O is OO BACK TO GENETICS PAGE

41 A B C 13. What is pleiotrophy? An inactive gene
A single gene which has multiple effects C A recessive gene that shows in the phenotype

42 Wrong, try again BACK TO QUESTION

43 RIGHT Pleiotrophy is a single gene which has multiple effects
An example would be Siamese cats BACK TO GENETICS PAGE

44 14. What is epistasis? A A gene that expressed in the genotype but not shown in the phenotype B A gene which effects multiple characteristics C Two recessive genes which cause dominance not to show

45 Go Back and Try Again! BACK TO QUESTION

46 You’re Right!!! An epistasis is two recessive genes that cause dominance not to show An example would be snapdragons BACK TO GENETICS PAGE

47 15. What is polygenic inheritance?
A single gene which has multiple effects B A gene which shows no characteristics C A dominant trait that is not expressed

48 Nope, try again BACK TO QUESTION

49 RIGHT!!! Polygenic Inheritance is a single gene which has multiple effects An example would be in skin color and height BACK TO GENETICS PAGE

50 16. An environmentally produced phenotype that stimulates the effects of a particular gene is called: A Genetic Drift B Industrial Melanism C A Phenocopy

51 SORRY, GO BACK !!! BACK TO QUESTION

52 Correct!!!! An environmentally produced phenotype that stimulates the effects of a particular gene is called a phenotype Examples are tranquilizer BACK TO GENETICS PAGE

53 17. Which genetic defect is the inability to break down phenylalanine?
Tay-Sach’s Syndrome B Phenylketonuria C Huntington Disease

54 WRONG BACK TO QUESTION

55 RIGHT The genetic disease that effects the inability to break down phenylalanine is phenylketonuria. BACK TO GENETICS PAGE

56 18. Which genetic defect is characterized by lipids causing nervous system disorder?
Tay-Sachs Syndrome B Phenylketonuria C Huntington Disease

57 Go Back and Try Again! BACK TO QUESTION

58 ***RIGHT*** Tay-Sachs syndrome is characterized by lipids causing a nervous system disorder. BACK TO GENETICS PAGE

59 19. Which genetic disease starts at middle age with mild mental illness?
Tay-Sach’s Syndrome B Cystic Fibrosis C Huntington disease

60 Nope, try again BACK TO QUESTION

61 ~RIGHT~ Huntington disease is a genetic disease which starts at middle age with mild mental illness. BACK TO GENETICS PAGE

62 20. Which genetic defect has sickle shaped cells and abnormal hemoglobin?
Down Syndrome B Cystic Fibrosis C Sickle cell anemia

63 Sorry, wrong answer BACK TO QUESTION

64 Correct!!!! Sickle cell anemia is characterized by sickle shaped cells and abnormal hemoglobin. BACK TO GENETICS PAGE

65 21. Which genetic disease causes problems with blood clotting?
Sickle Cell Anemia B Hemophilia C Cystic Fibrosis

66 NO WAY!! BACK TO QUESTION

67 RIGHT Hemophilia is a genetic disease which causes problems with blood clotting. BACK TO GENETICS PAGE

68 22. What is the inability to distinguish red from green?
Sickle Cell Anemia B Hemophilia C Red-green colorblindness

69 SORRY, TRY AGAIN BACK TO QUESTION

70 CORRECT Red-green colorblindness is a genetic disorder which is characterized by the inability to distinguish red from green. BACK TO GENETICS PAGE

71 23. What genetic disease is known as trisomy21?
Down’s Syndrome B Tay-Sach’s Syndrome C Red-Green Colorblindness

72 **TRY AGAIN** BACK TO QUESTION

73 GOOD JOB The genetic disease also know as trisomy 21 is Down’s Syndrome. BACK TO GENETICS PAGE

74 24. Which genetic disease causes the deteriorating of muscles?
Cystic Fibrosis B Duchene’s Muscular Dystrophy C Down’s Syndrome

75 NOPE BACK TO QUESTION

76 RIGHT!!! Duchene’s Muscular Dystrophy is a genetic disease which causes the deteriorating of muscles. BACK TO GENETICS PAGE

77 25. Which genetic disease is caused by an X, X, and Y chromosome?
Klinefelton syndrome B Down’s Syndrome C Criduchat

78 WRONG ANSWER BACK TO QUESTION

79 CORRECT The genetic disease caused by an XXY chromosome is Klinefelton syndrome BACK TO GENETICS PAGE

80 26. Which genetic disease is characterized by a cat-like cry?
Criduchat B Down’s Syndrome C Hemophilia

81 **TRY AGAIN** BACK TO QUESTION

82 ALRIGHT! The genetic disease characterized by a cat-like cry is Criduchat. BACK TO GENETICS PAGE

83 A B C 27. What is deletion? Sections of the chromosome are inverted
Sections of the chromosome are duplicated C Sections of the chromosome are deleted

84 Try again BACK TO QUESTION

85 RIGHT!!!! Deletion happens when sections of the chromosomes are deleted. BACK TO GENETICS PAGE

86 A B C 28. What is inversion? Sections of the chromosome are switched
Sections of the chromosome are duplicated C Sections of the chromosome are deleted

87 Sorry, Wrong Answer BACK TO QUESTION

88 Yep! Inversion is when sections of the chromosome are switched.
BACK TO GENETICS PAGE

89 A B C 29. What is translocation?
A section of one chromosome switches with a section of another chromosome B Sections of the chromosome are switched C A section of the chromosome is deleted

90 Try again BACK TO QUESTION

91 Good answer Translocation is when a section of one chromosome switches with another chromosome. BACK TO GENETICS PAGE

92 A B C 30. What is duplication? Sections of the chromosome are deleted
Sections of the chromosome are switched C Sections of a chromosome replicate more than once

93 Wrong Answer BACK TO QUESTION

94 Alright! Duplication is when sections of a chromosome are duplicated more than once. BACK TO GENETICS PAGE

95 31. What is nondisjunction?
There is a duplication of the chromosome B The homologous chromosomes do not separate at interphase C One X chromosome is duplicated in chromosome 23

96 SORRY, TRY AGAIN BACK TO QUESTION

97 GOOD JOB Nondisjunction is when the homologous chromosomes do not separate at interphase. BACK TO GENETICS PAGE

98 A B C 32. What is expressivity?
The degree to which a particular gene is expressed B There is a duplication of chromosome 21 C Recessive genes are expressed instead of dominant genes

99 Go back and try again BACK TO QUESTION

100 RIGHT!!! Expressivity is the degree to which a particular gene is expressed. An example would be sickle cells BACK TO GENETICS PAGE

101 A B C 33. What is polyploidy? Chromosome 21 duplicates more than once
There are more than two complete sets of chromosomes C The X chromosome is expressed twice along with a Y chromosome

102 NOPE, GO BACK BACK TO QUESTION

103 RIGHT!!! Polyploidy is when there are more than two complete sets of chromosomes. BACK TO GENETICS PAGE


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