You are on page 1of 8

BioMG1350 Prelim.

2- K Spring 2014 - ANSWER KEY  

DO NOT OPEN THE EXAM UNTIL


INSTRUCTED!
The exam will start at 9:05 and end at 9:55

While you wait to start the exam, please fill out your name, ID and version of this
test on the Scantron form. Do NOT fill out your birthdate

m
er as
co
eH w
LAST NAME (space) FIRST NAME 7 DIGIT STUDENT ID NUMBER

o.
rs e
Make sure you fill in the information clearly; only use #2 pencil
ou urc
• TURN OFF CELL PHONES AND ALL ELECTRONIC DEVICES. Anyone
found touching an electronic device will be assumed to be cheating, and the
o

test removed.
aC s

• Put ALL belongings under your seat.


vi y re

• If you finish before 9:50, you may hand in your Scantron and leave.
AFTER 9:50 YOU MUST STAY IN YOUR SEAT UNTIL THE END OF THE
EXAM AND ALL EXAMS HAVE BEEN HANDED IN.
ed d
ar stu

• At the end of the exam, hand in just the Scantron form; you
may keep this set of questions.
• Suggestions: indicate your answers on the test and then
sh is

transfer them to the Scantron.


Th

• Answer the easy questions first, and go back to the harder


ones.
• Mark only one response per question (the Scantron will
invalidate any answers with more than one entry)
• GOOD LUCK!

https://www.coursehero.com/file/12081236/Prelim-2-SP14/ The  exam  starts  on  the  next  page  


BioMG1350 Prelim. 2-K Page 2

Q1.   The  version  of  this  test  is:  


  1.   Version  K            ß          THIS  IS  YOUR  VERSION,  PLEASE  ENTER  THIS  ANSWER  IN  THE  FORM!    
  2.   Version  L  
 
Q2.   Many  proteins  are  completely  synthesized  in  the  cytosol  and  then  targeted  to  the  appropriate  organelle.    
For  which  of  the  following  organelles  is  this  not  the  case:  
  1.   Mitochondrion  
  2.   Nucleus  
  3.   Chloroplast  
  4.   Peroxisome  
  5.   It  is  true  for  all  of  these  organelles  
 
Q3.   You  are  studying  a  nuclear  protein  and  want  to  identify  its  nuclear  localization  sequence.  If  you  use  
molecular  genetics  to  express  a  construct  lacking  the  first  ten  amino  acids  of  your  protein,  it  fails  to  go  into  the  
nucleus.    If  you  express  a  construct  of  the  ten  amino  acid  sequence  fused  to  a  normally  cytoplasmic  protein,  you  find  
that  the  fusion  protein  is  cytosolic.    Which  of  the  following  statements  would  be  true  about  the  ten  amino  acid  
sequence:  
  1.   It  is  necessary  and  sufficient  to  target  a  protein  to  the  nucleus    

m
  2.   It  is  not  necessary  nor  sufficient  to  target  a  protein  to  the  nucleus  

er as
  3.   It  is  not  necessary  but  is  sufficient  to  target  a  protein  to  the  nucleus  

co
  4.   It  is  necessary  but  not  sufficient  to  target  a  protein  to  the  nucleus  

eH w
  5.   None  of  the  above  
 

o.
Q4.   Which  of  the  following  molecules  require  a  receptor  to  pass  through  a  nuclear  pore:  
  1.  
rs e
ATP  
ou urc
  2.   GTP  
  3.   A  20  kilodalton  protein  
  4.   A  100  kilodalton  protein  
  5.   Both  3  and  4  
o

     
Q5.   You  are  studying  nuclear  import.  You  mutate  the  only  nuclear  import  receptor  in  a  cell  so  that  it  cannot  bind  
aC s

Ran-­‐GTP  but  can  still  bind  a  cargo  protein.    Which  of  the  following  statements  would  correctly  describe  what  would  
vi y re

happen:  
  1.   The  import  receptor  would  be  found  both  in  the  cytosol  and  nucleus  with  bound  cargo  
  2.   The  import  receptor  would  accumulate  in  the  cytosol  with  bound  cargo  
  3.   The  import  receptor  would  accumulate  in  the  nucleus  with  bound  cargo  
  4.   The  import  receptor  would  accumulate  in  the  cytosol  without  bound  cargo  
ed d

  5.   The  import  receptor  would  accumulate  in  the  nucleus  without  bound  cargo  
ar stu

 
Q6.   Which  of  the  following  statements  is  wrong  regarding  import  of  proteins  into  mitochondria:  
  1.   The  precursor  protein  is  first  translated  in  the  cytosol  
  2.   The  protein  is  folded  after  it  is  transported  
sh is

  3.   The  signal  sequence  binds  a  receptor  in  the  outer  membrane  


  4.   Translocation  across  both  membranes  is  coupled  
Th

  5.   None  of  the  above  statements  are  wrong  


     
Q7.   What  fraction  of  the  different  proteins  synthesized  in  a  cell  are  made  on  the  endoplasmic  reticulum?  
  1.   About  1%  
  2.   About  10%  
  3.   About  30%  
  4.   About  50%  
  5.   About  80%  
 
 
 
 
 

                                                                                                             The  exam  continues  on  the  next  page  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/
BioMG1350 Prelim. 2-K Page 3

The  diagram  at  right  shows  the  membrane  of  the  endoplasmic  reticulum  and  relates  to  Questions  8-­‐10.  
 
Q8.   Which  of  the  indicated  components  is  involved  in  slowing,  
or  stopping,  translation  
  1.   A  
  2.   B  
  3.   C  
  4.   D  
 
Q9.   Which  of  the  components  is  necessary  to  relieve  the  
slowed,  or  stopped,  translation?  
  1.   A  
  2.   B  
  3.   C  
  4.   D  
 
Q10.   Which  of  the  components  is  rapidly  degraded?  
  1.   A  

m
  2.   B  

er as
  3.   C  

co
  4.   D  

eH w
 
Q11   In  the  diagram  of  the  sequence  of  a  membrane  protein  shown,  if  the  signal  sequence  is  removed  after  the  

o.
protein  is  synthesized,  how  many  times  will  the  polypeptide  chain  cross  the  membrane  
  1.  
rs e
Two  times  
ou urc
  2.   Three  times  
  3.   Four  times  
  4.   Five  times  
  5.   Six  Times  
o

 
Here  is  a  list  of  some  of  the  organelles/compartments  found  in  cells;  this  relates  to  questions  12-­‐17.  
aC s

  A.   cis  Golgi  
vi y re

  B.   Early  endosome  
  C.   Lysosome  
  D.   Endoplasmic  reticulum  
  E.   trans-­‐Golgi  network  
 
ed d

Q12.   In  which  organelle/compartment  does  the  first  step  of  N-­‐linked  glycosylation  occur?  
ar stu

  1.       A    
  2.   B  
  3.   C  
  4.   D  
sh is

  5.   E  
 
Th

Q13.   In  which  organelle/compartment  are  proteins  destined  for  regulated  secretion  sorted  from  those  destined  
for  constitutive  secretion:  
  1.   A  
  2.   B  
  3.   C  
  4.   D  
  5.   E  
 
 
 
 
 
 

                                                                                                             The  exam  continues  on  the  next  page  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/
BioMG1350 Prelim. 2-K Page 4

Q14.   In  which  organelle/compartment  are  mis-­‐folded  secretory  proteins  retained  and  then  subject  to  
degradation:  
  1.   A  
  2.   B  
  3.   C  
  4.   D  
  5.   E  
 
Q15.   From  which  organelle/compartment  do  COPI  vesicles  transport  material  from:  
  1.   A  
  2.   B  
  3.   C  
  4.   D  
  5.   E  
 
Q16.   From  which  organelle/compartment  do  COPII  vesicles  transport  material  from:  
  1.   A  
  2.   B  

m
  3.   C  

er as
  4.   D  

co
  5.   E  

eH w
 
Q17.   From  which  organelle/compartment  do  clathrin  vesicles  transport  material  from:  

o.
  1.   A  
  2.   B  
rs e
ou urc
  3.   C  
  4.   D  
  5.   E  
 
o

Q18.   If  the  t-­‐SNARE  present  on  the  plasma  membrane  was  removed,  which  of  the  following  things  would  start  to  
happen:  
aC s

  1.   Lysosomal  enzymes  would  be  secreted  


vi y re

  2.   Secretory  proteins  would  build  up  in  the  endoplasmic  reticulum  


  3.   Secretory  proteins  would  build  up  in  post-­‐Golgi  secretory  vesicles  
  4.   The  LDL  receptor  would  continue  take  up  LDL  normally  
  5.   Secretory  proteins  would  no  longer  be  subject  to  N-­‐linked  modification  
 
ed d

Q19.   If  a  transport  vesicle  is  accidentally  made  without  a  v-­‐snare,  which  of  the  following  events  would  not  
ar stu

happen:  
  1.   Cargo  would  be  packaged  into  the  transport  vesicle  
  2.   Adaptins  would  associate  with  the  vesicle  
  3.   The  vesicle  would  become  tethered  
sh is

  4.   The  vesicle  would  fuse  with  its  target  membrane  


  5.   The  vesicle  would  have  bound  Rab-­‐GTP  
Th

 
Q20.    If  dynein  is  absebnt,  which  of  the  following  things  will  occur:  
  1.   The  Golgi  will  disperse  
  2.   The  endoplasmic  reticulum  will  collapse  
  3.   Transport  from  the  endoplasmic  reticulum  to  the  Golgi  will  be  affected  
  4.   Both  1  and  2  
  5.   Both  1  and  3  
 
 
 
 
 
 
 

                                                                                                             The  exam  continues  on  the  next  page  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/
BioMG1350 Prelim. 2-K Page 5

The  scientists  Mike  Brown  and  Joe  Goldstein  established  the  receptor-­‐
mediated  uptake  of  LDL  (Low  Density  Lipoprotein)  by  analyzing  cells  
from  patients  with  hypercholesterolemia.  The  diagram  shows  normal  
LDL  receptor  (A),  and  two  mutant  receptors  (B  and  C)  from  such  
patients,  with  the  location  of  the  mutation  indicated  by  a  star.This  
relates  to  questions  21  and  22.  
 
Q21.   Which  of  these  receptors  cannot  bind  LDL:  
  1.   A  
  2.   B  
  3.   C  
  4.   B  and  C  
  5.   All  can  bind  LDL  
 
Q22.   If  you  treat  cells  to  neutralize  the  pH  of  the  early  endosome,  which  of  these  receptors  will  get  trapped  in  an  
early  endosome  with  bound  LDL  
  1.   A  
  2.   B  

m
  3.   C  

er as
  4.   A  and  B  
B  and  C  

co
  5.  

eH w
 
Q23.    In  which  of  the  following  organelles  do  proteins  from  the  secretory  pathway  first  meet  up  with  material  

o.
from  the  endocytic  pathway  
  1.  
rs e
The  Golgi  apparatus  
ou urc
  2.   The  endoplasmic  reticulum  
  3.   The  early  endosome  
  4.   The  lysosome  
  5.   They  never  meet  up  
o

 
Q24.    The  pathway  for  delivery  of  lysosomal  enzymes  to  lysosomes  was  elucidated  by  studying  cells  from  patients  
aC s

in  which  lysosomal  enzymes  did  not  get  to  lysosomes.    One  of  these  diseases  is  called  I-­‐cell  disease  -­‐  the  lysosomal  
vi y re

enzymes  fail  to  be  appropriately  modified  in  the  Golgi  for  recognition  by  the  lysosomal  enzyme  receptor.    In  cells  from  
a  patient  with  I-­‐cell  disease,  which  of  the  following  statements  is  correct:  
  1.   The  lysosomal  enzyme  receptor  would  be  degraded  
  2.   The  lysosomal  enzymes  would  be  degraded  in  the  trans-­‐Golgi  Network  
  3.   The  lysosomal  enzyme  receptor  would  be  stuck  in  the  trans-­‐Golgi  Network  
ed d

  4.   The  lysosomal  enzyme  receptor  would  be  stuck  in  the  early  endosome  
ar stu

  5.   The  lysosomal  enzyme  receptor  would  cycle  normally  between  the  trans-­‐Golgi  Network  and  the  
early  endosome  
   
Q25.   Which  phase  of  the  cell  cycle  is  most  variable  in  duration  between  different  cells  in  an  animal:  
sh is

  1.   M  
  2.   G1  
Th

  3.   S  
  4.   G2  
 
Q26.   During  which  phase  of  the  cell  cycle  is  M-­‐cyclin  synthesized  
  1.   M  
  2.   G1  
  3.   S  
  4.   G2  
 
 
 
 
 
 

                                                                                                             The  exam  continues  on  the  next  page  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/
BioMG1350 Prelim. 2-K Page 6

The  diagram  at  right  relates  to  questions  27-­‐31  and  shows  inactive  M-­‐Cdk  with  two  
sites  phosphorylated    
 
Q27.   What  is  the  component  labeled  B:  
  1.   CDK  
  2.   M-­‐Cyclin  
  3.   APC  
  4.   The  kinetochore  
  5.   Kinesin  
 
Q28.   Component  B  is  necessary  for  M-­‐Cdk  activity  because:  
  1.   Without  component  B,  component  A  cannot  bind  ATP  
  2.   It  moves  an  inhibitory  loop  in  the  structure  of  component  A    
  3.   Component  A  is  degraded  without  component  B  
 
Q29.   How  is  M-­‐Cdk  activated:  
  1.   By  additional  phosphorylation  
  2.   By  removal  of  inhibitory  phosphate  

m
  3.   By  removal  of  activating  phosphate  

er as
 

co
Q30.   Which  of  the  following  is  activated  by  a  positive  feedback  loop  to  fully  activate  M-­‐Cdk:  

eH w
  1.   Wee1  kinase  
  2.   Cdk-­‐activating  kinase  (CAK)  

o.
  3.   Cdc25  phosphatase.  
 
rs e
ou urc
Q31.   How  is  active  M-­‐Cdk  turned  off  when  the  checkpoint  in  mitosis  is  satisfied:  
  1.   By  phosphorylation  of  the  inhibitory  site  
  2.   By  removal  of  the  activating  phosphate  
  3.   By  degradation  of  component  A  
o

  4.   By  degradation  of  component  B    


 
aC s

Q32.   p53  is  a  human  protein  called  the  'guardian  of  the  genome'.    Which  statements  about  p53  is  false:  
vi y re

  1.   It  is  activated  by  DNA  damage  


  2.   It  is  stably  present  in  cells  with  no  DNA  damage  
  3.   It  becomes  phosphorylated  upon  DNA  damage  
  4.   p53  is  a  transcription  factor  that  regulates  expression  of  a  gene  encoding  a  Cdk  inhibitor  protein  
 
ed d

Q33.   At  which  checkpoint  do  cells  arrest  if  DNA  synthesis  is  not  complete:  
ar stu

  1.   Checkpoint  in  mitosis  


  2.   G2  checkpoint  
  3.   G1  checkpoint    
  4.   None  of  the  above  
sh is

 
Using  this  list,  answer  questions  34-­‐36     A.   Telophase  
Th

          B.   Metaphase  
          C.   Prometaphase  
          D.   Anaphase-­‐Metaphase  transition  
          E.   G1  phase  
          F.   G2  phase  
          G.   S  phase  
          H.   Prophase  
Q34.   When  do  cohesins  first  function:  
  1.   B  
  2.   C  
  3.   D  
  4.   G  
  5.   H  
 

                                                                                                             The  exam  continues  on  the  next  page  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/
BioMG1350 Prelim. 2-K Page 7

Q35.   When  do  cohesins  get  degraded:  


  1.   A  
  2.   C  
  3.   D  
  4.   F  
  5.   S    
 
Q36.   The  kinetochore  is  assembled  on  chromosomes  during:  
  1.   B  
  2.   C  
  3.   D  
  4.   F  
  5.   H  
 
Q37.   Microtubule  disassembly  at  kinetochores  during  anaphase  is  involved  in  
  1.   Sliding  of  inter-­‐polar  microtubules  
  2.   Movement  of  chromosomes  to  poles  
  3.   Activation  of  the  checkpoint  in  mitosis  

m
  4.   Kinesin  5-­‐dependent  movement  

er as
  5.   Movement  of  spindle  poles  apart  

co
   

eH w
 
Q38.   During  anaphase  B,  dynein  is  involved  in:  

o.
  1.   Sliding  of  inter-­‐polar  microtubules  
  2.  
rs e
Movement  of  chromosomes  to  poles  
ou urc
  3.   Activation  of  the  checkpoint  in  mitosis  
  4.   Kinesin  5-­‐dependent  movement  
  5.   Movement  of  spindle  poles  apart  
 
o

Q39.  Which  type  of  signaling  uses  membrane-­‐bound  signals?  


    1.  Paracrine  
aC s

    2.  Neuronal  
vi y re

    3.  Contact-­‐dependent  
    4.  Endocrine  
    5.  More  than  one  of  the  above    
 
Q40.  An   investigator   is   studying   the   effect   of   hormones   on   cells   and   sets   up   the   following   experiment:   First,   he   takes  
ed d

blood  from  rats  that  have  been  stressed  by  extreme  exercise.  Then  he  uses  the  blood  to  treat  3  different  types  
ar stu

of   cells   which   he   is   growing   on   independent  


dishes.   The   following   day,   he   observes   cells  
under  the  microscope  and  notices  that  cells  A  
have   proliferated   dramatically,   while   cells   B  
sh is

have   changed   their   morphology.   The   cells   in  


plate   C   secrete   proteins   that     turn   the   media  
Th

red.   The   investigator   explores   the   following  


hypotheses   to   explain   the   results   from   the  
experiment.   Based   on   the   information  
provided   and   your   knowledge   on   cell  
signaling,   indicate   which   one   provides   a   valid  
explanation:  
 
1. All  three  cell  types  contained  the  same  receptor  for  a  single  hormone  in  the  blood  of  the  rat.  
2. The  three  cell  types  responded  to  a  unique  hormone,  but  they  had  different  receptors.  
3. The  effects  were  triggered  by  three  different  hormones,  each  being  bound  by  a  different  receptor  in  each  
cell  type.    
4. All  of  the  above.  
5. None  of  the  above  
 

                                                                                                             The  exam  continues  on  the  next  page  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/
BioMG1350 Prelim. 2-K Page 8

Indicate  whether  the  following  statements  about  cell  signaling  are  TRUE  OR  FALSE.    
Q41.  Steroid  hormone  receptors  elicit  changes  in  cell  behavior  faster  than  those  elicited  by  channel-­‐coupled  
receptors.  (1=TRUE;  2=FALSE)  
Q42.  Second  messengers  are  small  molecules  that  are  produced  in  large  quantities  inside  the  cell  upon  reception  of  a  
signal.  (1=TRUE;  2=FALSE)  
Q43.  In  order  to  stay  alive,  cells  need  to  receive  signals  constantly.    (1=TRUE;  2=FALSE)  
Q44.  Drugs  can  have  secondary  effects  when  they  target  components  of  a  signal  transduction  pathway  that  control  
multiple  effectors  within  a  cell.  (1=TRUE;  2=FALSE)      
Q45.  Fill  in  the  space  in  the  following  statement  using  one  of  the  options  below:  “When  two  signals  share  a  common  
component  of  their  intracellular  signaling  pathway,  this  common  component  is  said  to    ___________  the  two  
signals  to  elaborate  a  single  response.”    
1. Relay.  
2. Transduce.  
3. Integrate.  
4. Distribute.  

m
5. Amplify.  

er as
Q46.  Indicate  which  one  of  the  statements  below  about  meiosis  is  TRUE:  

co
1. During  the  first  meiotic  cell  division,  the  spindle  separates  sister  chromatids.    

eH w
2. During  the  second  meiotic  cell  division,  homologous  chromosomes  undergo  recombination.    
3. The  first  meiotic  cell  division  is  very  similar  to  mitosis,  but  the  resulting  cells  are  haploid  because  the  DNA  

o.
does  not  replicate  previously.  
rs e
4. More  than  one  statement  is  true.    
ou urc
5. None  of  the  statements  is  correct.    
 
Q47.  Which  one  of  the  following  adult  tissues  originates  from  the  ectoderm  germ  layer:  
1. Gut,  liver  and  lungs.    
o

2. Skeleton  and  muscle.  


3. Heart  and  blood.  
aC s

4. Nervous  system.    
vi y re

5. None  of  the  above.    


 
THE  FOLLOWING  TEXT  AND  DRAWING  REFER  TO  QUESTIONS  Q48  TO  Q51  (see  below):    
A  graduate  student  is  performing  a  transplantation  experiment  in  bird  embryos.  To  be  able  to  trace  the  origin  of  cells  
ed d

after  the  transplantation,  he  uses  two  different  species  of  birds  which  have  a  different  pigmentation.  He  uses  as  
donor  tissue  a  region  of  the  hindlimb  (leg)  of  pink-­‐pigmented  bird  embryos.  He  transplants  this  piece  to  the  anterior  
ar stu

region  of  the  forelimb  (wing)  primordia  of  a  blue-­‐pigmented  bird.  The  transplanted  tissue  heals  and  the  graduate  
student  finds  that  the  treated  wing  in  the  resulting  blue-­‐pigmented  bird  develops  normally  and  contains  some  pink-­‐
pigmented  areas  in  the  anterior  part.  Indicate  whether  the  following  statements  are  TRUE  or  FALSE:  
sh is
Th

 
Q48.  The  fate  of  the  transplanted  tissue  was  to  become  wing.  (1=TRUE;  2=FALSE)  
Q49.  The  transplanted  tissue  was  already  determined  to  become  wing  before  the  transplantation  (1=TRUE;  2=FALSE)    
Q50.  The  transplanted  tissue  was  specified  as  wing  tissue  after  the  transplantation  (1=TRUE;  2=FALSE)    
Q51.  In  this  experiment  some  cells  could  induce  others  to  change  their  fate  (1=TRUE;  2=FALSE)  

                                                                                                             This  is  the  last  page  of  the  exam  


https://www.coursehero.com/file/12081236/Prelim-2-SP14/

Powered by TCPDF (www.tcpdf.org)

You might also like