CAS BI 105 Lecture Notes - Lecture 11: Primase, Helicase, Tyrosine
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DNA REPLICATION:
Start with the DNA Strand in a eukaryotic cell: CTAGGGATTACCATAGGATACAGA
1. Where in the cell is this strand found?
Nucleus
Let’s say this is a gene, and during replication it is changed to: CTAGGGATTACCAAAGGATACAGA.
2. What type of mutation is this?
Missense
3. Will it cause a change in the protein product produced? Why/why not? (Hint: you may want to come
back to this question after finishing question 16).
Yes.
DNA Strand: CTAGGGATTACCATAGGATACAGA
Assume this strand is a template strand being used in DNA replication.
4. What would be the sequence of the new strand being made?
GAUCCCUAAUGGUAUCCUAUGUCU
5. How many of the enzymes involved in DNA replication can you name? What are their roles?
Helicase, RNA Polymerase, DNA Polymerase, Primase, Topiomerase
6. If you are going through DNA replication, how many DNA strands did you start with, and how many
do you end with?
7. When does DNA replication occur (what phase of the cell cycle)?
The S Phase
TRANSCRIPTION:
DNA Strand: CTAGGGATTACCATAGGATACAGA
This is a gene. Before it is a promoter region with the sequence CCCGTATGGATAA. A mutation is
acquired in this promoter region so that it has changed to CCCGTAG.
8. What do you think will happen to the gene as a result?
A) No change to the gene
B) It will never be translated
C) Translation is unaffected but it will not be replicated during DNA replication.
This gene is going to go through transcription.
9. What enzyme is required?
RNA Polymerase
10. What will the resulting molecule be called?
The mRNA Transcript
11. Transcribe this DNA strand here: GAUCCCUAAUGGUAUCCUAUGUCU
12. Where in the cell does transcription take place?
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Document Summary
Why/why not? (hint: you may want to come back to this question after finishing question 16). Before it is a promoter region with the sequence cccgtatggataa. Take the molecule you ended up with after transcription and write it here: Now let"s use epigenetics to control the making of this gene. The epigenetic mechanisms we studied were: methylation, acetylation, alternative splicing, differing lengths of the cap and tail, sirna, microrna, protein activation. The process we explored in the first 3 pages can be summarized as this: Apply each of the epigenetic mechanisms to the right place in this process. For each epigenetic mechanism, label it as: the protein product is more likely to be made, there will be less protein product made or protein production will be delayed, protein production will be prevented. We discussed some of these epigenetic mechanisms within the context of biotechnology.