00:01
So you're looking at a target dna sequence up here.
00:04
So you want to use pcr to amplify this region.
00:08
So what method is used to cause the two strands of dna to come apart, which is called denaturation? so in the lab, you're going to heat up the dna to 95 degree celsius.
00:22
The heat is going to denature dna.
00:27
As i just mentioned, denaturation means the two strands of dna separate.
00:35
Due to the heat breaking down the hydrogen bond between the nitrogen base.
00:41
So after the denaturation, the two strands of dna separate.
00:45
One strand has only a and the other strand has only t.
00:56
Now, to amplify this dna sequence, you will need primers.
01:02
So the question asks you to figure out the primers that you will need to finish the pcr reaction.
01:08
So you'll need two primers.
01:10
One primer is complementary to the top strand.
01:13
I'm going to use red color.
01:15
So it's going to be five prime end on the right side and all t's, which will amplify the top strand, three.
01:26
And then the other primer you'll need is going to be the green one, which is going to be complementary to the bottom strand.
01:32
And again, they have opposite orientation, five on the left side and three on the right.
01:37
So you'll need these two primers, which is going to be complementary to the bottom strand.
01:39
Going to be the b answer for the question.
01:43
So now this is question four.
01:45
Let's take a look at five, which is asking about transcription.
01:49
So you can see that on a board, you'll have a dna strand, and then only partial region is being transcribed.
02:05
So this is a gene that being transcribed and produced single strand in m rna.
02:11
So first of all, draw a box around the label, the promoter and terminator of this gene.
02:19
Now, a promoter region is always upstream of the transcription initiation side, which is right here.
02:25
So the red box right here is the promoter region, which initiate transcription.
02:31
The terminator is somewhere here at the end of the transcribed gene.
02:35
Terminator is a sequence that tells the enzyme rite polymerase to take off from the gene or dna, so the mrna will be released.
02:46
So now i draw the promoter region and terminal region.
02:51
What enzyme synthesized rna product? so the enzyme that transcribe the gene from dna to mrna is called rna polymerase.
03:07
So the enzyme, this is mrna, is called rna polymerase.
03:14
That makes sense because rna polymerase preliminized rna.
03:22
So rna polymerase synthesize the product, which is rna.
03:42
Now, the next question, where in the cell occurred? so obviously, the location, i'll just add them in the end, rna polymerase mrna in the nucleus of eukaryotic, organism.
04:01
The nucleus is the location where this process happens.
04:06
The next question, initiation of transcription occurs at what part of the g? so the initiation happens at promoter region.
04:29
This is because promoter region has certain sequence we call potato box that is going to recruit the rna polymerase...