Lecture 4 Flashcards

1
Q

What is the common structure properties of nucleotides like RNA and DNA?

A

➢ One to three phosphate group(s)
➢ a pentose (5-carbon atom) sugar,
➢ a nitrogenous base (a pyrimidine or purine)

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2
Q

What bases are purines? structure difference?

A

Adenine & Guanine
- have two cylical shapes (pentagon and hexagon)

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3
Q

What bases are pyrimidines?
structure diff?

A

Thymine, Uracil and Cytosine
- have ONLY ONE cyclical shape

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4
Q

What sugar and base is ONLY in RNA?

A

-Ribose (containing two OH group)
- Uracil instead of thymine

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5
Q

What sugar and base is ONLY in DNA?

A
  • Deoxyribose (containing one OH and one H)
    -Thymine instead of Uracil
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6
Q

What are nucleotide functions as monomers?

A
  • Building Blocks of Nucleic Acids (DNA & RNA)
    -Energy carriers (cell energy currency), carrying high-energy
    bonds between phosphate groups (e.g. ATP, GTP)
    -Form coenzymes (essential for enzymatic activity)
    -Intracellular signalling molecules (e.g. cyclic AMP)
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7
Q

What is the structure of the DNA/RNA strand/ backbone?

A

In DNA/RNA, nucleotides are covalently linked to form polynucleotide strand (backbone)
▪ via phosphodiester bonds, linking 5’ phosphate of one nucleotide to the 3’ OH of the next
▪ Creating a 5’-to-3’ directionality
▪ Nucleic acids of human cells has a 5’ end and a 3’ end
➢ (e.g., 5’-TCG-3’)

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8
Q

What is the structure of B DNA?

A

DNA (in B form) has two helical grooves of different widths, providing binding sites
for proteins/drugs
➢ major - wider
➢ minor - narrower

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9
Q

What is the advantage to RNA being single stranded?

A

▪ dsRNA (double stranded) is possible in nature. Many viruses contain dsRNA genomes.
▪ Immune cells recognise dsRNA as a viral signature, triggering antiviral responses.

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10
Q

What is DNA denaturation?

A

DNA Denaturation → separation of the DNA double strands into single strands
* DNA renaturation → When conditions are reversed, H bonds can be reformed →

▪ High temperatures (90-100°C) break H-bonds between complementary nucleotides
▪ Higher G-C content increases DNA stability than A-T. (3 H-bonds vs 2) thus more energy needed
▪ Principles of the PCR technique to amplify specific regions of DNA

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11
Q

What is a gene?

A

A DNA segment that encode specific, inheritable traits.
* Nucleotide sequence in genes determine the specific amino acid sequence of certain
proteins through the GENETIC CODE (DNA → RNA → PROTEINS)– Lec. 4
* Human genome has ≈ 25,000 genes (<1.5% of DNA)

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12
Q

Where is DNA found in eukaryotic cells?

A

Nuclear DNA in the nucleus
Mitochondrial DNA in the mitochondria

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13
Q

What is DNA replication?

A

DNA replication is the process by which DNA makes a copy of itself, before cell divisions
▪ Each chromosome will result in 2 identical DNA (sister chromatids)
▪ Copied DNA is segregated into daughter cells
▪ Occurs in the nucleus during the S phase of interphase

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14
Q

What type of process is DNA replication?

A

DNA replication is a SEMI-conservative process

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15
Q

What are the four stages to DNA Rep?

A
  1. Replication Fork Formation
  2. Initiation
  3. Polymerase elongation
    4.Termination
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16
Q

Describe Replication Fork Formation

A
  • DNA replication starts at a sequences called
    origin of replication (rich in A - T)
  • At each, DNA is denatured by initiator proteins
  • Helicase enzymes unwind/unzip the DNA
    double strands bidirectionally, by breaking H-
    bonds, creating two Y-shaped replication forks
17
Q

Describe initiation

A
  • DNA polymerase requires an RNA primer, created
    by primase enzyme, to initiate synthesis
  • DNA polymerase attaches to the 3’ end of the primer
    and synthesises new DNA strand in the 5’->3’
    direction, using the parental strand as a template
  • DNA polymerase forms phosphodiester bonds
    between nucleotides, extending the new DNA strands
  • The process requires deoxynucleotide triphosphates
    (dNTPs) to drive the reaction
18
Q

Describe elongation

A

Replication of leading strand is continuous
▪ Same direction as the growing replication forkReplication of the lagging strand is discontinuous
▪ It requires many RNA primers
▪ Synthesis in short DNA fragments (Okazaki
fragments), each initiated by a new RNA primer

19
Q

Describe termination

A

A nuclease degrades RNA primers
➢ The gaps are filled by DNA polymerase
➢ The enzyme DNA ligase joins adjacent Okazaki
fragments → DNA Replication is complete

20
Q

What is a benefit of DNA Polymerase?

A

DNA polymerase has proofreading activity to check &
correct base-pairing errors
▪ When a mismatch occurs, DNA polymerase removes the
incorrect nucleotide and replaces it with the correct one.

21
Q

What does DNA helicase do?

A

Unwinds parental double helix

22
Q

What does DNA ligase do?

A

Joins Okazaki fragments and seals other breaks in sugar-phosphate backbone

23
Q

What does primease do?

A

Synthesise RNA primers for DNA polymerase to start the polymerisation process

24
Q

What does DNA topoisomerase do?

A

Unravel twists in DNA that occur as a result of DNA replication