DNA structure, DNA replication, Transcription, Translation, Mutations Flashcards

1
Q

Based on Griffith’s experiment, mice lived when:

Injected with heat killed S strain cell components of S. pneumoniae

Injected with live R + live S strains of S. pneumoniae

Injected with heat killed R strain cell components + live S strain of S. pneumoniae

Injected with live S strain of S. pneumoniae

A

Injected with heat killed S strain cell components of S. pneumoniae

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2
Q

Based on Chargaff’s rule, if a dsDNA has 40%As then the DNA should have______Cs.

  5% 
  10% 
  40% 
  20% 
  50%
A

10%

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3
Q

In the Hershey and Chase experiment 35S labeled bacteriophages were found in _______, while 32P labeled bacteriophages were found in__________.

  nucleus, Endoplasmic Reticulum (ER) 
  supernatant, supernatant 
  pellet, supernatant 
  supernatant, pellet 
  pellet, pellet
A

supernatant, pellet

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4
Q

The elongation of the leading strand during DNA replication__________

  is carried out by DNA polymerase III 
  produces Okazaki fragments 
  progresses away from the replication fork 
  occurs in the 3’ to 5’ direction 
  All options are true.
A

is carried out by DNA polymerase III

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5
Q

Primases are enzymes that synthesize primers for DNA replication in cells. Which of the following sequences could potentially serve as a primer to replicate the DNA sequence below (in cells)?

5’-ATCGGAACATTACG-3’

  3’-AUCATA-3’ 
  5’-CCTTGT-3’ 
  3’-UUGUAA-5’ 
  5’-TTTTTT-3’ 
  All options are correct
A

3’-UUGUAA-5’

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6
Q

Think back to Hershey and Chase experiment using 32P and 35S labeled bacteriophages. Hypothetically, if they would have found 35S labeled bacteriophages in the pellet, then they would have concluded that:

  Protein was the genetic material 
  RNA was the genetic material 
  DNA was the genetic material 
  Carbohydrates were the genetic material 
  Lipids were the genetic material
A

Protein was the genetic material

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7
Q

Which of the following is TRUE for both Prokaryotic DNA polymerase III and RNA polymerase?

Both enzymes need a primer to add nucleotides to

Both enzymes make a new strand of RNA in 3’ to 5’ direction

Both enzymes add new nucleotides in 5’ to 3’ direction

Both enzymes form peptide bonds to make new polymers

Both enzymes are used in transcription

A

Both enzymes add new nucleotides in 5’ to 3’ direction

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8
Q

What is the correct order of use of enzymes/proteins in DNA replication?

a) SSB
b) Helicase
c) Primase
d) DNA pol I
e) DNA pol III
f) DNA Ligase

A B D C E F
B A C E D F
A B C D E F
B A C D E F

A

B A C E D F

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9
Q

Which statement below about pre-mRNAs and mRNAs is TRUE?

pre-mRNA has introns and exons, while mature mRNA has only exons

there is no difference between pre-RNA and mature mRNA

pre-mRNA is in Prokaryotes, while mRNA is in Eukaryotes

pre-mRNA is made using DNA polymerases while mRNA is made using RNA polymerase

pre-mRNA has a 5’ cap and a 3’ poly A tail, while mature mRNA does not

A

pre-mRNA has introns and exons, while mature mRNA has only exons

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10
Q

What is a role of the ER signal sequence (peptide) in protein transport in a cell?

It is used to help proteins enter the nucleus
It is used to make new proteins
It is used to help proteins enter the ER
It is used to help proteins go to Golgi from ER
It is used to mark proteins for hydrolysis

A

It is used to help proteins enter the ER

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11
Q

What is the difference between the leading strand and the lagging strand in DNA replication?

The leading strand requires an RNA primer, whereas the lagging strand does not.

The leading strand is synthesized in the 5’ to 3’ direction while the lagging strand is synthesized in the 3’ to 5’ direction.

The leading strand is synthesized in the 3’ to 5’ direction in a discontinuous fashion, while the lagging strand is synthesized in the 5’ to 3’ direction in a continuous fashion.

The leading strand is synthesized continuously in the 5’ to 3’ direction, while the lagging strand is synthesized discontinuously in the 5’ to 3’ direction.

A

The leading strand is synthesized continuously in the 5’ to 3’ direction, while the lagging strand is synthesized discontinuously in the 5’ to 3’ direction.

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12
Q

What is the role of tRNAs in cells?

tRNAs are used in translation at ORI.

tRNAs are used in translation. They bring amino acids to be added to the polypeptide chain.

tRNAs are used in transcription. They are needed to separate the two DNA strands

tRNAs are used in transcription. They are needed to convert pre mRNA to mRNA

tRNAs are used in translation to help transport mRNA out of the nucleus

A

tRNAs are used in translation. They bring amino acids to be added to the polypeptide chain.

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13
Q

Which of the following mutations will likely be MOST harmful for protein structure/function?

silent mutation

missense mutation changing a polar amino acid to a polar amino acid

deletion of signal peptide

frameshift mutation

nonsense mutation at the end of the gene

A

frameshift mutation

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14
Q

Which of the following is a correct statement about gene expression (transcription and translation)?

In Prokaryotes, transcription and translation occur in the cytoplasm while in Eukaryotes transcription and translation occur in the nucleus

In Prokaryotes, transcription occurs in the nucleus while in Eukaryotes it occurs in the cytoplasm

In Prokaryotes and Eukaryotes transcription occurs in the nucleus while translation occurs in the cytoplasm

In Prokaryotes transcription and translation occur in the cytoplasm while in Eukaryotes transcription occurs in the nucleus while translation occurs in the cytoplasm.

A

In Prokaryotes transcription and translation occur in the cytoplasm while in Eukaryotes transcription occurs in the nucleus while translation occurs in the cytoplasm.

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15
Q

Match function with its corresponding enzyme/protein: This enzyme helps add polyA tails

PolyA Polymerase
Spliceosome
Primase
topoisomerase
DNA Ligase
DNA polymerase I
A

PolyA Polymerase

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16
Q

Match function with its corresponding enzyme/protein: This complex of proteins and snRNA is used in splicing

PolyA Polymerase
Spliceosome
Primase
topoisomerase
DNA Ligase
DNA polymerase I
A

Spliceosome

17
Q

Match function with its corresponding enzyme/protein: This enzyme is used to make RNA primers

PolyA Polymerase
Spliceosome
Primase
topoisomerase
DNA Ligase
DNA polymerase I
A

Primase

18
Q

Match function with its corresponding enzyme/protein: This enzyme helps to relieve overwound DNA

PolyA Polymerase
Spliceosome
Primase
topoisomerase
DNA Ligase
DNA polymerase I
A

topoisomerase

19
Q

Match function with its corresponding enzyme/protein: If this enzyme is defective, then there will be RNA in DNA

PolyA Polymerase
Spliceosome
Primase
topoisomerase
DNA Ligase
DNA polymerase I
A

DNA polymerase I

20
Q

Match function with its corresponding enzyme/protein: If this enzyme is defective, then gaps between DNA fragments will not be sealed

PolyA Polymerase
Spliceosome
Primase
topoisomerase
DNA Ligase
DNA polymerase I
A

DNA Ligase

21
Q

determine which process will be directly involved/affected: Promoter sequences are mutated

Transcription
Translation
RNA splicing
Replication

A

Transcription

22
Q

determine which process will be directly involved/affected: Pre mRNA is used as a template

Transcription
Translation
RNA splicing
Replication

A

RNA splicing

23
Q

determine which process will be directly involved/affected: Release factor is not present

Transcription
Translation
RNA splicing
Replication

A

Translation

24
Q

determine which process will be directly involved/affected: Helicase is mutated and not functional

Transcription
Translation
RNA splicing
Replication

A

Replication

25
Q

determine which process will be directly involved/affected: Peptidyl transferase is mutated and not functional

Transcription
Translation
RNA splicing
Replication

A

Translation

26
Q

determine which process will be directly involved/affected: GTP is needed

Transcription
Translation
RNA splicing
Replication

A

Translation