Unit 1: Human Cells - Key Area 2 - Structure and replication of DNA Flashcards

1
Q

What does DNA consist of?

A

Units called nucleotides

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2
Q

What are nucleotides made of?

A

Phosphate, deoxyribose sugar, and a base

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3
Q

What forms the genetic code?

A

The base sequence

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4
Q

What holds each strand of DNA together?

A

Each individual strand of DNA is held together by a strong chemical bond between the phosphate of one nucleotide and the carbon 3 of the sugar, on another nucleotide.

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5
Q

What holds the bases in adjacent strands together and what does this cause?

A

Weak hydrogen bonds hold the bases together and make them coil into a double helix structure.

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6
Q

What does the 3’ end of a DNA strand have?

A

A deoxyribose sugar

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7
Q

What does the 5’ end of a DNA strand have?

A

A phosphate

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8
Q

What end can nucleotides only be added to?

A

The 3’ end.

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9
Q

How many different nucleotides are there and what causes them to be different?

A

There are 4 different nucleotides, depending on the base they have.

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10
Q

What are the 4 different bases?

A

Adenine, Cytosine, Guanine and Thymine

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11
Q

What do the 2 DNA strands have running in different directions?

A

Their phosphate backbone.

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12
Q

What is the double helix described as having?

A

The Double helix is described as having two anti-parallel chains of nucleotides because one side goes from 5’ to 3’ and the opposite side goes from 3’ to 5’.

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13
Q

What is DNA arranged in?

A

Tightly coiled chromosomes.

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14
Q

What is DNA polymerase and what is its function?

A

DNA polymerase is an enzyme that controls the formation of the sugar-phosphate bonding of the nucleotides into the DNA strand.

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15
Q

What is a primer?

A

A short sequence of nucleotides at the 3’ end.

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16
Q

What strand has to be replicated in fragments?

A

The lagging strand (5’ end).

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17
Q

What is the 5’ end also called and why is this?

A

The lagging strand because it has to be replicated in fragments and is slower than the 3’ end.

18
Q

What is the 3’ end also called?

A

The leading strand.

19
Q

What is ligase and what does it do?

A

Ligase is an enzyme that joins all the DNA fragments together once they are all in place.

20
Q

For DNA replication to occur, what must the nucleus contain?

A

Primers, DNA (Template), Enzymes(Ligase and DNA Polyemrase), ATP and Nucleotides (the 4 types).

21
Q

Where does DNA replication occur?

A

In the nucleus.

22
Q

What is the first thing that happens to the DNA molecule in the DNA replication process?

A

A DNA molecule unwinding.

23
Q

What happens to the DNA molecule after it has unwound in DNA replication?

A

The hydrogen bonds between the adjacent bases are broken and these bases act as a template for a new DNA strand to be made.

24
Q

What happens after the nucleotides are exposed in DNA replication?

A

Free-floating nucleotides in the nucleus join on to their complementary bases. This happens simultaneously along the DNA strand.

25
**Which end of the DNA** can **nucleotides be added to**?
The **3’ end.**
26
How do you know which end of a DNA strand is the **5’ end**?
It is **joined** to a **phosphate**.
27
Why is **DNA replication important**?
**DNA replication** is **important** so that **when cells divide** they have to have **the correct genetic information** they need to function properly **and that no information is lost**.
28
**Why** is a **primer needed** in DNA **replication**?
**A primer is needed** in DNA replication because DNA polymerase can **only add nucleotides to a pre-existing chain**.
29
What is the **function** of **the PCR**?
PCR **_amplifies_ DNA**. ( It creates many copies of a piece of DNA in vitro).
30
What does the **amplification of DNA** involve the use of?
The **amplification of DNA involves the use of primers**. Each primer is a short strand of DNA complementary to a specific target sequence at the 3' end of the strand to be replicated.
31
What are the **steps** involved in **PCR**?
* **DNA is heated (94–96 °) to separate**/denature the DNA stands. * I**t is then cooled (50–65 °C)** to allow the primers to bind to the target sequence of DNA. * **Heat tolerant DNA polymerase at 72 °C** then adds nucleotides to the primers (at the 3' end of the original DNA strands). * **Repeated cycles of heating and cooling** amplify the region of DNA. * **The first cycle of replication produces 2 identical; DNA molecules**, the second produces 4 molecules and so on and in an hour a short length can become a million.
32
What is the **first process of PCR** called which is **carried out at 94 - 96 degrees** celsius?
**Denaturation**/separation.
33
What happens in **the first stage of PCR**?
The **DNA is heated** so **it is denatured** and the **weak hydrogen bonds** between the bases **are broken** to leave two single strands.
34
What is the **second process of PCR** called where **the temperature is cooler** at around **68 degrees** celsius?
**Annealing**
35
What is the **last process of PCR** called which is carried out about **72 degrees** celsius?
**Elongation**
36
What are the **practical uses of PCR**?
* **Solve crimes** - if not enough DNA is found to work on it can be amplified so the forensics people have more to work with (DNA profiling). * **Diagnosing genetic disorders** - testing for cystic fibrosis etc. * **Settiling paternity disputes** using (DNA profiling).
37
What is **the role of ligase**?
**Joins fragments of DNA at the 5' end** strand/ lagging strand.
38
What is the **role of DNA polymerase**?
**Adds nucleotides to the 3' end** of a strand when there is a pre-existing chain and primer.
39
The 5' end is replicated in fragments, whilst the 3' end strand is replicated continuously. **Explain why the strands are replicated in different ways**?
DNA **polymerase can only add nucleotides at _the 3' end_ of a growing strand**.
40
What happens to the **primers** in the **second stage of PCR**?
The **primers bind** or anell **to the target sequence of DNA**.
41
Why is **the temperature raised again** in the **third process of PCR**?
So **the temperature** is **closer to the optimum temperature** for DNA polymerase **to add nucleotides** to the primers.