Lecture Notes Beginning Week 9-End ‘ Flashcards

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1
Q

What are the mechanisms of DNA replication?

A

Unwinding of the DNA strands- Initiation of Replication- Elongation of the DNA strands being replicated-Termination of Replication

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2
Q

Origins of replication are associated with a _____.

A

Bubble

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3
Q

Each replication bubble has _____ replication forks.

A

2

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4
Q

Which order of strands are continuous?

A

From the origin of replication, 3’ to 5’ strands are continuous.

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5
Q

Define Replication Fork

A

A y-sharped region of the replicating DNA where the parental DNA strands are being unwound and the replication of DNA takes place.

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6
Q

Define Origin of Replication

A

A region of DNA that has specific nucleotide sequences where the DNA replication begins.

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7
Q

Define Helicases

A

Enzymes that untwist the double helix at the replication forks, separating the 2 strands and making them available as templates.

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8
Q

Which enzyme is responsible for releasing the tension in DNA strands?

A

Topoisomerase.

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9
Q

Define Topoisomerase

A

An enzyme that breaks, swivels, and rejoins the DNA strands. During the replication of DNA, this enzyme helps relieve the strain in the double helix ahead of the replication fork. T-BSR

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10
Q

Define Single Strand Binding Proteins

A

Proteins that bind to the unpaired DNA strands during DNA replication, stabilizing them and holding them apart while they serve as templates for the synthesis of the complementary DNA strands.

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11
Q

Define Primase

A

AN RNA Polymerase that joins RNA nucleotides to make the primer using the parental DNA strands as a template.

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12
Q

Define DNA Polymerase III

A

A complex of enzymes that catalyzes the elongation of new DNA by adding nucleotides to the 3’ end of an existing chain. In elongates in the 5’ to 3’ direction and READS in the 3’ to 5’ direction.

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13
Q

What is an important thing to note about DNA Polymerase III?

A

It can only add nucleotides to the free 3’ end of a sequence of nucleotides and CANNOT do it by itself. It needs the primase enzyme to add a sequence of ribonucleotides.

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14
Q

The _____ end has to be free to allow for further binding.

A

3’

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15
Q

What is the bond formed between the carbon ends and the phosphate groups of another nucleotide?

A

Phosphodiester Bond

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16
Q

What happens to the phosphates in the phosphate group when DNA polymerase allows for the binding of nucleotides?

A

2 inorganic phosphates get released in the cytoplasm and the nuclear matrix.

17
Q

_____ must be removed; this is done by _____.

A

Primers-DNA Polymerase I

18
Q

Define DNA Polymerase I

A

An enzyme that removes and replaces the RNA primer.

19
Q

Define Ligase

A

An enzyme that ligates the ends of DNA molecules.

20
Q

What is the main difference between leading strands of DNA and lagging strands of DNA?

A

The main difference is that the leading strand is continuous and the lagging strand is in Okazaki fragments.

21
Q

Define Okazaki Fragments

A

Short of sections of DNA. Formed at the time of discontinuous synthesis of the lagging strand during replication of DNA.

22
Q

What is meant by the proofreading activity of DNA polymerase?

A

Polymerase has the ability to check each nucleotide against the template soon after it is added to the growing strand. In real life, we find 1 in 10 million mistakes.

23
Q

How do mismatched nucleotides evade DNA polymerase proofreading?

A

They evade proofreading or occur after DNA replication because of the exposure of cells to things such as chemical carcinogens and UV light.

24
Q

How is the mismatched nucleotide problem fixed?

A

Thymine Dimer distorts the DNA molecule
A nuclease enzyme cuts the damaged DNA strands at two points.
DNA polymerase fills the gap.
DNA ligase seals the remaining nick.

25
Q

How many enzymes aid in the fixing of nucleotide mismatching? What is a defect in these enzymes associated with?

A

We have about 130 enzymes. Defects of one of these enzymes is associated with colon cancer.

26
Q

What happens in the process of chromatin packing ?

A

Proteins called histones allow for the wrapping of strands to make nucleosome beads. The beads pack together. The domains further loop and get more and more condensed.

27
Q

What histones are available to us? What histones do the nucleosome contain?

A

H1, H2A, H2B, H3, H4 ate available to us.

H2A,H2B,H3,H4 are contained in the nucleosome (2 of each).

28
Q

Which histone is not present in the histone octamer? Where is it located?

A

H1; it is attached near the nucleosome.

29
Q

What are histone modifications?

A

Methylation of Histones leads to the condensation of DNA and PREVENTS transcription of genes.

Acetylation of Histones leads to the decondensation of DNA and ALLOWS for the transcription of genes.