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Sample Questions, Exam III 1. Snapdragons have a sincle gene (locus) that determines flower color. The allele R is for red flowers and it shows incomplete dominance over the recessive allele r for white flowers. What color flowers are produced by Rr plants? a. All red b. Mixed red and white (some flowers of each color) c. pink d. white with pink streaks e. purple 2. An allele at one locus affects several phenotypic traits (e.g. cystic fibrosis is caused by a single defective gene which causes clogged blood vessels, sticky mucus, salty sweat, liver failure, etc.). This is an example of: a. continuous variation. b. codominance. c. incomplete dominance. d. epistasis. e. pleiotropic effects. 3. A human is heterozygous at a blood group locus and expresses both genotypes (e.g. they have type AB blood). This is an example of: a. polygenic inheritance. b. codominance. c. incomplete or partial dominance. d. pleiotropy. e. complete dominance. 4. Occasionally, a gene at one chromosomal locus affects the phenotypic expression of a second gene found at an entirely different chromosomal locus. This phenomenom is called: a. pleiotropy. b. partial dominance. c. epistasis. d. secondary regulation. e. polygenic inheritance. 5. An example of a sex-linked human genetic-based disorder is: a. Duchene muscular dystrophy. b. sickle cell anemia. c. HuntingtonÕs disease. d. cystic fibrosis. e. Tay-Sachs disease. Genes located on the same chromosome are said to be: a. polygenic. b. bottlenecked. c. pleiotropic. d. linked. e. epistatic. 6. 7. A human autosomal recessive lethal genetic disease whose defective allele has been maintained at a relatively high level in certain population groups because it gives the heterozygote resistance to an infectious disease is: a. Tay-Sachs disease. b. cystic fibrosis. c. sickle-cell anemia. d. muscular dystrophy. e. HuntingtonÕs disease. _______________________________________________________________________ 8. Four genes (A, W, E, and G) on a chromosome have the following linkage map: The lowest recombination frequency would be observed between genes: a. A and W. b. W and E. c. E and G. d. A and E. e. A and G. _______________________________________________________________________ 9. Thomas Morgan was a. b. c. d. e. the first person to: map a specific gene/trait to a specific chromosome. observe codominance. carry out amniocentesis. observe crossing over under the microscope. define genetic variation. 10. An example of a human genetic condition caused by an autosomal dominant defective gene/allele: a. KlinefelterÕs syndrome. b. Down syndrome. c. HuntingtonÕs disease. d. cystic fibrosis. e. Turner. 11. An inactivated ÒXÓ chromosome in a human female cell is seen as a/an: a. centrosome. b. Barr body. c. genetic imprint. d. nucleosome. e. centromere. 12. An early theory explaining the basis of evolution suggested organisms could alter their phenotype by use or disuse of a character (stretch the neck, for example) and that such aquired characteristics could be passed on to the following generation. The scientist best known for this theory was: a. Lamarck. b. Mendel. c. Morgan. d. Darwin. e. Barr. 13. The primers for DNA synthesis in E. coli cells are: a. short segments of DNA which contain many errors. b. special proteins called primases. c. short RNA molecules. d. synthesized by reverse transcriptase. e. E. coli DNA polymerase does not require a primer. 14. An example of a human genetic disease involving a male with a a. Klinefelter syndrome. b. Down syndrome. c. HuntingtonÕs disease. d. Turner syndrome e. muscular dystrophy. Barr body is: 15. The human chromosomes which are not either the "X" or "Y" chromosomes are collectively called _________. a. mosaics b. sex chromosomes c. karyotypes d. monosomics e. autosomes 16. A human gene is said to be sex-linked if: a. it is more common in females than males. b. it is found on the ÒYÓ chromosome. c. it is encoded by the ÒXÓ chromosome. d. it is expressed only in males. e. it is recessive in males. 17. The structure shown to the right is an example of a: A. purine. B. pyrimidine. C. ribose sugar. D. deoxyribose sugar. E. molecule not found in DNA. 18. Which of the following is not a source of microevolution? a. genetic drift b. mutation c. random mating d. natural selection e. All of the above are sources of microevolution. 19. All of the following conditions are requirements for maintaining HardyWeinberg equilibrium in a population EXCEPT: A. random mating. B. no migration. C. a high net mutation rate. D. large population size. E. no natural selection. 20. Throughout history, the migration of people on Earth has steadily increased. This movement has changed human evolution by increasing the: a. nonrandom mating. b. bottleneck effect. c. genetic drift. d. mutation rate. e. gene flow. 21. Two males and two females are the first colonists on Mars. After many generations, the population of Mars has a high allele frequency for color blindness. This is most likely due to: a. the bottleneck effect. b. gene flow. c. assortative mating. d. the founder effect. e. mutation. 22. The red flower allele exhibits incomplete dominance over the white flower allele. Using the Hardy-Weinberg equation (p2 + 2pq + q2 = 1), if the frequency of the red allele in a popopulation is 0.8 and the frequency of the white allele is 0.2, what is the fraction of plants which will have pink flowers? a. 4% b. 8% c. 16% d. 32% e. 64% 23. During DNA replication, the "lagging strand" is synthesized as a series of small DNA fragments which are later connected into a continuous DNA molecule. These short segments are called : a. Okazaki fragments. b. replicons. c. replication forks. d. transcription units. e. Griffith units. 24. The enzyme which unwinds the DNA helix, allowing replication to occur is called: a. primase. b. DNA replicase. c. reverse transcriptase. d. helicase. e. DNA litigase. 25. The DNA from cells grown many generations in 14N medium and then switched to 15N medium for one generation would give a pattern after CsCl gradient centrifugation looking like: (a) (b) (c) (d) (e) ____________________________________________________________________________ 26. DNA replication in bacteria occurs by a _____________ mechanism as demonstrated by the experiment of ___________. a. semi-conservative, Chargaff b. c. d. e. conservative, Messelson and Stahl dispersive, Avery and Mcleod semi-conservative, Messelson and Stahl conservative, Watson and Crick 27. The enzyme which covalently connects the short DNA fragments synthesized on the lagging strand (i.e. "ties" them together) is called: a. DNA nuclease. b. DNA polymerase. c. helicase. d. DNA ligase. e. primase. 28. The enzyme which extends the primers, making the new DNA strand at the replication fork is: a. DNA polymerase I. b. primase. c. RNA polymerase. d. DNA replicase. e. DNA polymerase III. 29. Okazaki is best known for: a. his experiments which showed DNA replication occurs in a semiconservative manner. b. his experiments which showed tha DNA is the genetic material. c. his experiments which showed that genes encode proteins. d. his experiments which showed the direction of DNA synthesis. e. his experiments which showed DNA on the lagging strand of a replication fork is synthesized in short pieces. 30. Griffith used rodents and strains of Streptococcus pneumoniae (the bacterial species he used were at that time known as Pneumococcus) to demonstrate: a. that DNA is the genetic material. b. DNA replication occurs semiconservatively. c. bacterial transformation. d. protein coats of bacteriophage are not required for successful infection. e. German bombs can adversely affect experimental results. The structure of DNA molecules was first elucidated by: a. Watson and Crick. b. Avery. c. Franklin and Wilkins. d. Griffith. e. Beadle and Tatum. 31. 32. Alfred Hershey and Martha Chase used 32P and 35S radioactively-labeled bacteriophage show that: a. DNA can be selectively labeled by 35S atoms. b. bacteriophage proteins can be specifically labeled by 32P. c. entry of bacteriophage proteins into the bacterium correlated well with the subsequent production of progeny bacteriophage. d. DNA is the genetic material of T2 bacteriophage. e. the phospholipid membrane of bacteriophage does not transfer genetic material from one generation to the next. 33. Which of the following is NOT true of the presently accepted model for the structure of DNA? a. It is a double helix. b. The two strands are antiparallel. c. The bases are located on the interior of the helix. d. The two strands are complementary. e. All of the above are true of this model for DNA structure. 34. The experiment by Avery (using the method of Griffith) utilized which of the following to demonstrate that DNA is the genetic material? a. Cesium chloride (CsCl), ultracentrifugation, 14N, 15N, E. coli b. 32P, 35S, T2 bacteriophage, E. coli c. TMV virus, RMV virus, tobacco plants d. Pneumococcus, DNase, RNase, protease, lipase (digests lipids) e. X-ray crystallography 35. Chargaff’s studies lead him to conclude: a. that the amount of adenine (A) in the DNA from an organism always equaled the amount of thymine (T) in the DNA from the same organism. b. that DNA was a helix. c. that the lactose operon was inducible. d. that DNA was in fact the genetic material responsible for bacterial transformation. e. he should have gone to medical school and made real money. 36. The whooping crane population fell to less than 2 dozen individuals earlier in this century. From the point of population genetics, this group of individuals might be expected to show substantial evidence of: a. natural selection. b. pleitrophy. c. the bottleneck effect. d. Only answers ÒaÓ and ÒcÓ are likely to be true. e. All of the above are likely to be true. 37. The X-ray crystallography pictures critical to the discovery of the structure of DNA were obtained by: a. Franklin and Wilkins. b. Watson and Crick. c. Avery and Griffith. d. Beadle and Tatum. e. Messelson and Stahl. 38. The individual nucleotides which make up a single strand of DNA are connected to the nucleotides above and below them (or to the 5Õ and 3Õ sides if you prefer--NOT CONNECTING TWO STRANDS OF THE DUPLEX to each other) by: a. peptide bonds. b. hydrogen bonds. c. phosphodiester bonds. d. reversible bonding. e. faith. 39. In a DNA duplex, the base A is always paired with: a. guanine. b. cytosine. c. d. e. thymine. uracil. deoxyribose. 40. The base pairs between two strands of a DNA molecule are held together by: a. phosphodiester bonds. b. ionic bonds involving the phosphate groups. c. polar covalent bonds. d. hydrogen bonds. e. a combination of all of the above. 41. DNA polymerases do NOT require which of the following in order to synthesize new DNA? a. a primer b. a template c. deoxyribonucleotide triphosphates (dNTPs) d. ATP e. All of the above are required by DNA polymerases. 42. The protein that keeps the single-stranded DNA from rewinding at the replication fork during DNA replication is: a. DNA polymerase III. b. primase. c. ssb. d. helicase. e. DNA ligase. 43. The location on a chromosome where DNA replication begins is called a/an: a. origin (ori). b. promoter. c. centromere. d. telomere. e. initiator. 44. The scientist(s) who generated and characterized auxotrophic mutants of Neurospora to demonstrate that a gene gives rise to a single enzyme (really polypeptide) was/were: a. Watson and Crick. b. Fraenkle and Conrad. c. Abbot and Costello. d. Beadle and Tatum. e. Garrod 45. A population of flowers has a range of colors from white to pink to dark red. Deer eat the lighter colored plants to the point where their numbers are reduced in the population, giving the population a darker average color. This would be an example of: a. stabilizing selection. b. directional selection. c. diversifying selection. d. random selection. e. frequency-dependent selection. 46. The scientist credited with first proposing the chromosome theory of inheritance was: a. Garrod. b. c. d. e. Sutton. Ingram. Sanger. Mendel. 47. The enzyme which removes the primers during DNA replication is: a. primase. b. DNA polymerase III (DNAP III). c. gyrase. d. DNA polymerase I (DNAP I). e. helicase. 48. Which of the following carries out proofreading during DNA replication? a. DNA polymerases. b. helicases. c. gyrases. d. Ssb. e. primases. 49. A human with the XXY karotype is: a. phenotypically a male and no Barr body. b. phenotypically female. c. phenotypically male but with a Barr body. d. phenotypically female with no Barr body. e. frequency-dependent selection. 50. An example of a phenotypic female human with no Barr body would be someone with: a. an XXX karyotype. b. Down Syndrome. c. Kleinfelter Disease. d. Huntington Disease. e. Turner Syndrome. 51. A person with a karyotype of trisomy 21 will suffer from: a. Tay-Sachs. b. Down Syndrome. c. Kleinfelter Disease. d. Huntington Disease. e. Turner Syndrome. 52. The scientist(s) who first developed a method for determining the sequence/order of amino acids in a protein (e.g. insulin) was/were: a. Watson and Crick. b. Garrod. c. Hammerling. d. Ingram. e. Sanger. 53. Proofreading by a DNA polymerase a. the connecting process. b. the removal of c. the process of d. the removal of activity. describes: of the correct bases by the polymerization RNA primers by the 5Õexonuclease activity. forming the new hydrogen bonds between bases. improperly paired bases by the 3Õexonuclease e. the process by which DNA polymerases always get an ÒAÓ for on eplication exams. 54. The segment of DNA replicated from a single start point (the unit of DNA replication, 1 per bacterial chromosome) is called a/an: a. centrosome. b. replisome. c. replicon. d. gene. e. cistron. 55. A trait shows continuous variation within a population (e.g. humans). This suggests that the trait exhibits: a. a polygenic pattern of inheritance. b. pleiotrophy. c. incomplete dominance. d. codominance. e. linkage disequilibrium. height in