DNA Structure and Function Flashcards

1
Q

What does DNA stand for?

A

Deoxyribonucleic Acid

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2
Q

DNA is a polymer of ________, which are held together by ________ bonds.

A

nucleotides; phosphodiester

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3
Q

Label the 5’ end and the 3’ end of this single DNA strand.

A

The 3’ end carbon is attached to an -OH group and the 5’ end carbon is attached to a phosphate group.

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4
Q

Define:

the antiparallel nature of DNA.

A

The two strands of DNA that make up the double helix run in opposite directions, one strand with a 5’ -> 3’ orientation and the other with a 3’ -> 5’ orientation.

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5
Q

What are the three main parts of a nucleotide?

A

a phosphate group, a 5-carbon sugar, and a nitrogenous base

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6
Q

Name the purines and pyrimidines.

A

The purines are adenine and guanine. The pyrimidines are cytosine and thymine.

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7
Q

What is the difference in structure between purines and pyrimidines?

A

Purines are two ring structures while pyrimidines are single ring structures.

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8
Q

Which nitrogenous base forms hydrogen bonds with adenine?

A

thymine

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9
Q

Which nitrogenous base forms hydrogen bonds with guanine?

A

cytosine

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10
Q

Which type of bond forms between the nitrogenous bases of two complementary DNA strands?

A

hydrogen bond

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11
Q

How many hydrogen bonds form between adenine and thymine?

A

two hydrogen bonds

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12
Q

How many hydrogen bonds form between guanine and cytosine?

A

three hydrogen bonds

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13
Q

What is the central dogma of molecular biology?

A

DNA is transcribed to RNA which is translated to amino acids that make up a protein.

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14
Q

Define:

DNA helicase

A

an enzyme responsible for separating the two strands of a DNA double helix needed for initiation of DNA replication

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15
Q

What is the name of the enzyme responsible for adding deoxyribonucleotides to a newly created DNA strand during replication?

A

DNA polymerase

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16
Q

What does DNA polymerase require to get started?

A

DNA polymerase cannot begin adding nucleotides by itself. An RNA primer of approximately 10 ribonucleotides is required to which DNA polymerase can begin adding nucleotides.

17
Q

In what direction does DNA polymerase read the parental strand?

A

3’ -> 5’

18
Q

In what direction is the new complementary strand created by DNA polymerase?

A

5’ -> 3’

19
Q

What is the difference between the leading strand and the lagging strand?

A

The leading strand is the newly synthesized strand of DNA being replicated continuously due to the complementary parental strand’s 3’ -> 5’ direction towards the replication fork. The lagging strand is the newly synthesized strand of DNA that is replicated in a series of fragments (Okazaki fragments) due to the complementary parental strand’s 5’ -> 3’ direction towards the replication fork.

20
Q

Define:

**semiconservative **
in terms of DNA replication.

A

The semiconservative nature of replication means that when a new double helix is created, it contains one strand from the original DNA, and one newly synthesized strand.

21
Q

Which enzyme is responsible for making repairs during DNA replication?

A

DNA polymerase proofreads as it adds nucleotides to new DNA strands. When a mismatched nucleotide is detected, DNA polymerase re replaces it with the correct nucleotide.

22
Q

Define:

recombinant DNA

A

DNA whose two DNA strands have been artificially recombined.

23
Q

A __________ enzyme cuts a DNA strand at a specific nucleotide sequence that is usually palindromic.

A

restriction

24
Q

Define:

sticky ends

A

Sticky ends are complementary single stranded ends created by a restriction enzyme cut. A restriction enzyme will often cut a strand unevenly, creating sticky ends that can form base pairs with any DNA molecule that has a complementary sticky end.

25
Q

_________ ends are those caused by a restriction enzyme that cuts a DNA strand straight across, leaving no uneven ends that can hybridize.

A

Blunt

26
Q

Define:

hybridization

A

Hybridization is the process by which separated strands of DNA will spontaneously bond with either their original complementary partner or any other complementary strand.

27
Q

Which three kinds of double stranded combinations can be made from hybridization?

A
  • DNA-DNA
  • DNA-RNA
  • RNA-RNA
28
Q

Describe the process of:

gene cloning

A
  1. Cut human DNA and plasmid DNA with the same restriction enzyme.
  2. Insert human DNA restriction fragment into plasmid by mixing them together.
  3. Seal with DNA ligase.
  4. Insert plasmid into bacteria, where replication occurs.
29
Q

What use does an antibiotic resistant gene have during gene cloning?

A

Since the cloning process is not perfect, some bacteria will not have the desired plasmid. To get rid of this bacteria, an antibiotic resistant gene is necessary in desired plasmids. Bacteria that do not have the appropriate plasmid will be killed upon contact with the antibiotic, leaving only desired clones.

30
Q

Which two specific genes must a bacterial plasmid contain to eliminate undesirable bacteria in the gene cloning process?

A

The lacZ gene and an antibiotic resistance gene

31
Q

When active, what does the lacZ gene do?

A

An active lacZ gene allows bacteria to break down the sugar X-gal. When placed on a medium with X-gal, the active lacZ gene is indicated by blue.

32
Q

What purpose does an inactivated lacZ gene have in the gene cloning process?

A

An inactivated lacZ gene containing the desired DNA fragment cannot break down the sugar X-gal. When the cloned bacteria is put on a medium with X-gal, the inactive lacZ gene does not change color (like active lacZ gene would).

33
Q

The ________ gene allows for detection of desired DNA fragments while an _________ ____________ gene allows for detection of desired vectors.

A

lacZ; antibiotic resistance

34
Q

What does PCR stand for?

A

Polymerase Chain Reaction

35
Q

Why is PCR more beneficial than simply gene cloning?

A

PCR is a much faster method of cloning.

36
Q

Describe the process of:

PCR

A
  1. Target DNA is denatured to separate the double stranded DNA template.
  2. Many copies of two complementary DNA primers are mixed.
  3. The solution is cooled so primers can hybridize with the single stranded templates.
  4. Heat resistance polymerase is added to extend the primers.
37
Q

Which three items must be mixed for PCR to take place?

A

target DNA, two RNA primers, and a heat resistance polymerase