Practice Exam Questions for Biotechnology Lecture 1. Eco RI is an example of which type of enzyme? a. b. c. d. e.
reverse transcriptase RNA polymerase restriction endonuclease [CORRECT] DNA polymerase DNA ligase
2. The diagram is a restriction map of a circular plasmid DNA showing the recognition sites for the restriction endonucleases xyz I and xyz II. Which of the 5 lanes (A, B, C, D, or E) in the agarose gel show the DNA the fragments expected following a restriction digest of the plasmid using enzyme xyz II ONLY? [D is CORRECT]
3. If you discovered a bacterial cell that contained no restriction endonuclease, which of the following would you expect to happen? a. b. c. d. e. The cell would be unable to replicate its DNA. The cell would destroy all plasmids. The cell would be easily infected and lysed by bacterial viruses. [CORRECT] The cell would become an obligate parasite. Both a and d would occur.
4. Which of the following is a technique that is used to separate DNA molecules from each other by differential movement due to size and electrical charge? a. b. c. d. e. restriction enzymes gene cloning agarose gel electrophoresis [CORRECT] ampicillin DNA ligase
5. Which of the following procedures would be involved in demonstrating a Restriction Fragment Length Polymorphism (RFLP) in human DNA? a. incubating a mixture of single strand DNA from two closely related species with the enzyme reverse transcriptase b. incubating DNA nucleotides with DNA polymerase c. Southern Blotting [CORRECT] d. incubating RNA with DNA nucleotides and reverse transcriptase e. incubating DNA fragments with "sticky ends" with ligase
Short Answer 1.	
  	
  	
  	
  	
  	
  	
  	
  	
  2.	
  	
  	
  3.	
  	
  	
  	
  	
  	
  	
  4.	
  	
  	
  	
  5.	
  	
  	
  	
  Consider	
 the	
 DNA	
 sequence:	
  5'	
 ATCTA	
 3'	
  3'	
 TAGAT	
 5'	
  Is	
 this	
 sequence	
 a	
 "palindrome"?	
 Yes,	
 you	
 could	
 say	
 so.	
  Is	
 this	
 sequence	
 an	
 inverted	
 repeat?	
 NO	
  In	
 the	
 restriction	
 enzyme	
 name	
 "NotI",	
 what	
 does	
 the	
 "Not"	
 mean?	
  Refers	
 to	
 the	
 latin	
 binomial	
 name	
 of	
 the	
 bacterial	
 species	
 from	
 which	
 the	
 enzyme	
 was	
 isolated.	
  [Nocardia otitidis-caviarum, in case you are interested.]	
  How	
 do	
 restriction	
 enzymes	
 differ	
 from	
 other	
 (ordinary)	
 nucleases?	
 	
  The	
 most	
 important	
 difference	
 is	
 that	
 they	
 cut	
 DNA	
 molecules	
 reproducably	
 only	
 at	
 specific	
 recognition	
  sequences.	
  How	
 do	
 these	
 special	
 properties	
 make	
 them	
 useful	
 in	
 molecular	
 biology?	
  Allows	
 a	
 DNA	
 sample	
 to	
 be	
 repeatedly	
 	
 cut	
 up	
 into	
 families	
 of	
 identical	
 fragments	
 with	
 predictable	
 sizes.	
  What	
 is	
 the	
 natural	
 role	
 of	
 restriction	
 modification	
 systems	
 in	
 bacteria?	
  Probably	
 protection	
 against	
 infection	
 by	
 bacterial	
 viruses.	
  What	
 2	
 types	
 of	
 enzymes	
 are	
 involved	
 in	
 R-M	
 systems?	
  Endonuclease	
 and	
 methylase	
 
6.	
  	
 
Complete	
 the	
 following	
 example	
 of	
 a	
 R-M	
 sequence.	
 The	
 arrow	
 represents	
 a	
 site	
 of	
 strand	
 cutting	
 and	
 the	
 "*"	
  indicates	
 a	
 methylated	
 base.	
 
*
7.	
  	
  	
  	
  	
  	
  	
  	
  	
  Compute	
 the	
 average	
 frequency	
 of	
 the	
 restriction	
 site	
 above	
 in	
 a	
 DNA	
 with	
 40%	
 GC	
 base	
 pairs.	
  (0.3)	
 (0.2)	
 (0.2)	
 (0.2)	
 (0.2)	
 (0.3)	
 =	
 0.00014	
  What	
 would	
 be	
 the	
 average	
 restriction	
 fragment	
 size	
 in	
 kilobases?	
  1/0.00014	
 =	
 6944	
 bp	
 
8.	
  	
 
The	
 following	
 diagram	
 is	
 a	
 restriction	
 map	
 of	
 a	
 small	
 linear	
 DNA	
 molecule	
 containing	
 one	
 gene.	
 
BamHI EcoRI BamHI
1.0 kb 0.5 kb
0.1 kb
0.3 kb GENE
0.9 kb
EcoRI
Samples	
 of	
 this	
 DNA	
 are	
 digested	
 in	
 4	
 separate	
 tubes	
 with	
 different	
 combinations	
 of	
 restriction	
 enzymes	
 as	
  follows:	
  	
  Tube#:	
  1	
  2	
  3	
  4	
  Enzyme/s:	
  Control	
  EcoRI	
  BamHI	
  EcoRI	
 +	
 BamHI	
  	
  (no	
 enzyme)	
  	
  Unfortunately,	
 the	
 4	
 DNA	
 digests	
 were	
 not	
 labeled	
 properly,	
 and	
 were	
 mixed	
 up	
 while	
 loading	
 them	
 onto	
 an	
  agarose	
 gel.	
 The	
 stained	
 gel	
 looked	
 like	
 this:	
 
	
  Can	
 you	
 un-mix	
 the	
 samples?	
 i.e.	
 Can	
 you	
 determine	
 which	
 lane	
 of	
 the	
 gel	
 (A-D)	
 corresponds	
 to	
 each	
 tube	
 (1- 4)?	
  	
  Circle	
 all	
 the	
 bands	
 on	
 the	
 gel	
 that	
 containing	
 a	
 DNA	
 fragment	
 with	
 the	
 complete	
 sequence	
 of	
 the	
 gene.	
 Give	
  the	
 sizes	
 of	
 these	
 fragments.	
 
1
A
3
B
2
C
4
D
2.8 kb
1.2 kb
9.	
  The	
 following	
 diagram	
 is	
 a	
 restriction	
 map	
 of	
 a	
 small	
 circular	
 plasmid	
 DNA.	
 Two	
 genes	
 are	
 shown,	
 Amp-R	
 and	
  lacZ.	
 The	
 arrows	
 indicate	
 the	
 direction	
 of	
 transcription	
 for	
 these	
 genes.	
  	
 
EcoRI 0.4 kb BamHI 0.2 kb Amp-R EcoRI 0.7 kb SmaI 1.0 kb
1.1 kb lacZ
SmaI 0.3 kb EcoRI SmaI
	
  	
  What	
 is	
 the	
 total	
 size	
 of	
 the	
 plasmid	
 DNA	
 in	
 kilobases?	
  	
  4.8	
 kb	
 	
  	
  Determine	
 the	
 #	
 and	
 the	
 sizes	
 of	
 the	
 DNA	
 fragments	
 expected	
 when	
 the	
 plasmid	
 is	
 fully	
 digested	
 by	
 each	
 enzyme	
  combination	
 below.	
 List	
 the	
 fragments	
 in	
 order	
 of	
 decreasing	
 size	
 in	
 each	
 column	
 of	
 the	
 table.	
  	
  BamHI	
  EcoRI	
  SmaI	
  SmaI	
 +	
 BamHI	
  SmaI	
 +	
 EcoRI	
 +	
  BamHI	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  In	
 the	
 SmaI	
 +	
 EcoRI	
 +	
 BamHI	
 column	
 circle	
 the	
 fragment	
 that	
 would	
 contain	
 the	
 promoter	
 sequence	
 for	
 lacZ.	
 
EcoRI
0.5 kb
0.6 kb
	
  	
  BamHI	
  4.8	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  EcoRI	
  	
  	
  	
  1.6	
 (X2)	
  	
  	
  1.0	
  	
  0.6	
  SmaI	
  	
  2.7	
  	
  	
  1.4	
  	
  	
  0.7	
  SmaI	
 +	
 BamHI	
  	
  	
  2.5	
  	
  1.4	
  	
  	
  0.7	
  	
  	
  	
  	
  0.2	
  SmaI	
 +	
 EcoRI	
 +	
  BamHI	
  	
  	
  	
  	
  	
  1.1	
  1.0	
  0.7	
  0.6	
  0.5	
  0.4	
  0.3	
  0.2	
 
10. This problem is about the inheritance of color blindness caused by expression of an X-linked recessive allele. The recessive allele for color blindness is relatively common in the human population. A color-blind man (I-1) marries a woman with normal color vision (I-2). This couple's daughter (II-1) has normal vision and she marries a man with normal color vision (II-2). I. As a genetic counselor, what could you tell this family about the probability that their offspring (III-1) will be color-blind?
I-1
I-2
II-1
II-2
There is a 1/4 probability of a color-blind son.
III-1
You suggest that the family in question undergoes DNA testing. A pair of PCR primers is used to amplify a specific region from the human genome containing the gene for Xlinked color blindness. The normal allele of the gene has a variable restriction site for the enzyme Hind III that is missing in the color-blind allele. After amplifying DNA from the genomic DNA of each individual, the PCR product is digested with Hind III and the digests are then separated on an agarose gel.
I-1 I-2 II-1 II-2 III-1
800 kb 400 kb 200 kb
II. What would you tell the family now (based on the results of the DNA test)?
	
 
Now you can tell them they will have a daughter with normal vision but who is heterozygous for the recessive allele.