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00:25 Yeah. Okay. Welcome folks. right. Um, okay. The

00:49 one club be available uh, crops afternoon. It was gonna be

00:55 but told me they were doing some of maintenance thing. So,

01:00 so it should be available tomorrow afternoon the rest of the week.

01:05 speaking of that, let me just forward real quick. So distribution nearly

01:12 average. Um, so, do do, um, look at

01:20 exam when it's available tomorrow afternoon. a look at it. Um,

01:26 , if you've got questions, you know, go through because you

01:29 through some of the questions that you them. Um, let me very

01:35 . Um, Oh yeah, that's I should have put from the

01:38 So there's no answer key because everybody has a different combination of

01:43 Okay? So go through the, , you can figure out the answer

01:49 if you can't, then, you , certainly let me know, email

01:54 office hours will have you. So, but, but it's a

02:01 learning process for you to first look the example on your own.

02:07 Rather right away. Just email me , la, la la.

02:11 It's better for you just to give a chance to look at it.

02:14 obviously there's questions, let me Um, if even for the sake

02:21 justice, if I left up on question was completely, and it's just

02:25 that reason alone, look, look the MS question. So, I

02:30 , so anyway, so do that certainly arranged time to visit if you

02:37 to, if you didn't meet expectations God's sakes. Do not do the

02:41 thing again. Okay. Do not the same process of study again.

02:46 it up. Okay. Um to change it up is just gonna mean

02:53 the same result. It just trust me, I've been doing this

02:56 long to not know that. And the there's no shame in seeking

03:05 . Okay, so um so do . If you didn't meet expectations,

03:12 jump off a little bit, but reassess. Okay. And you

03:19 you need help with that as Let me know china. So uh

03:24 probably gonna have some good amnesia just . It's now the focus is exam

03:31 that which is uh still a ways obviously after spring break. Okay.

03:38 not even on exactly a week after break later that week. So um

03:46 so we're back to stuff being new . So backward quiz this week.

03:52 A smart work Islamic do although I somebody say it wasn't available. So

03:57 will check that. I'll check smart too. Does anybody else notice that

04:02 tried doing some artwork? Chapter 60 ? You have access? Okay then

04:07 will I will check that. Um Let's see. So okay,

04:14 gonna continue with viruses um into uh cycles today and uh and um and

04:25 half of likely to finish up halfway . If not sooner than that on

04:33 . And then the rest of thursday be Project Flipped Class on Chapter

04:39 Uh really just part one, part is more of the basics of

04:45 It's not really the the pathways and . It's more just kind of um

04:50 know, here is how really how gets the energy kind of thing.

04:55 , and so forth. So anyone through that stuff is available and um

05:01 then really 13, 13 14 is lot of metabolism, but don't let

05:07 we do out. Okay. So try to hopefully make it somewhat more

05:14 . Okay. Um and I said not going to have to memorize all

05:20 plus reactions on the tackle. Nor all the enzymes. It's just

05:25 a way I do it. That not that way. Okay, so

05:29 so don't be afraid of it. . Um it's actually metabolize probably one

05:35 my probably my favorite part of of . So, because it's the way

05:40 the way life works. Alright, metabolism. Okay. Same in the

05:46 as it is in you really. , but we're there let's let's continue

05:55 um, with viruses. Okay, this is kind of just a rehash

06:00 bit. So the last time was about part one was released about the

06:05 virus here is very structural components of uh vary. So here is really

06:12 focusing on structure and components of the . Um of course they're not

06:19 as we mentioned, they obviously require host the metabolism uh as other things

06:26 they have to remember the basic structure our alliances that protein the capsule surrounding

06:35 genome of RNA. The doesn't have envelope or not. Another important

06:46 Um the envelope derived from the host in fact. So um then other

06:55 of course are going to be envelope . Uh it's the captain. Uh

07:03 are typically involved in certainly in the or at the recognition of vote buying

07:09 entry into the host. Um the so remember the viral infection begins or

07:17 whether or not the virus can recognize appropriate help in fact. So we

07:24 have the terms thrown in. There not mentioned here but range and uh

07:31 is that tissue right there in a host. How many different types of

07:37 sells can infect? Okay. And can be broad ordinary. Okay.

07:43 let's see. So then we ended with classification. Right. So we

07:49 at different groups of viruses. So Baltimore classification is about genome type uh

07:59 RNA double strategy and then the route takes to get to the um

08:07 R. Writes the M. D. Of course is the point

08:10 which you can then translate into viral . Okay. And so remembering that

08:16 we're gonna rehash this again because the group here can be the RNA

08:22 And so it's always important to remember the endgame is the virus at some

08:28 . Right. For some viruses, more or less immediate, Others can

08:34 prolonged. Okay. Uh and that what when does it begin producing viral

08:41 ? Right, viral project. so it's going to take over to

08:45 at some point and make it a using factor. Okay. And uh

08:51 time for that to happen again, virus type but eventually it's gonna do

08:58 might make lots of viral particles. does that have to have lots of

09:02 synthesis? Right. Make lots of protein components right now to make the

09:08 that make uh any other necessary proteins assemble it all. But the genome

09:15 , not talking the genome. So that's what the endgame is.

09:21 And so it's just, you depending on the viral type, it

09:25 take a kind of a circuitous route you will to get there.

09:31 And so again, the plus minus virus system just plus minus gonna pay

09:37 together. Right? So the fact we're talking about those types right?

09:43 RNA virus and mine is right. just has to do with the with

09:50 acid based pairing rules relationship. Um the has to be its complementary stand

09:58 referred to one is plus someone as as the plus track campaigns coding

10:02 Okay. It can be directly um and it can be directly translating this

10:10 . Okay, so maybe it's Maybe it's a minus strength.

10:14 And the minus strand has to then copied into a plus strength. Okay

10:19 one of the things I remember is plus strand is always a plus our

10:22 and it's always the the mmr it's one that is translated. Okay.

10:27 the other thing to remember is if tournament minus any virus. Yes it

10:33 to copy that to make this make transcript to make transit into proteins.

10:39 it also has to make copies of minus G. M. Because that's

10:43 gonna be stuck into all these little is gonna make it's making viral because

10:50 a dinosaur and virus. So everything comes out of the whole cell have

10:55 have that genome. Right so it's going to take that and then go

11:01 to this right? Making minus RNA for the purpose of popping them

11:08 All the different caps have been Okay so uh and so you keep

11:15 in mind that that plus strand I copied until minus is copied into A

11:22 . Right? My um strand is into a plus. Okay come

11:27 So just just just the way it . Okay like that. Mm hmm

11:34 hmm mm hmm mm hmm. Okay again we'll move cash this again as

11:43 go through today uh we go through specific Vira types. Okay. Any

11:50 about this stuff at this point? . The roof. Okay so one

12:01 time. That's what I like. ? No that only because it's a

12:16 Arnie box. So in order to gonna have to launch a cognitive in

12:21 to reason for our project. So the it is it is.

12:29 even this one. All right. this one uh when it has to

12:35 lots of copies of this as it just turns out that they can

12:39 both as an actor and as a itself. So, I guess to

12:45 your question. Yeah. Having to that. Yeah. Because the double

12:53 RNA has both. So you don't to work that you didn't. All

12:57 . Just take his minus pocket until train and then off it goes.

13:07 . Oh sorry. Sure. Let's here. Any other questions. Okay

13:20 let's um alright so this is actually last thing we wanted to talk

13:25 This is the last slide of the and stuff. And again, do

13:28 memorize this table. I just just to point out you know, just

13:33 uh some of the viruses you're probably with. My point here is really

13:39 point out the number of RNA viruses we have with the flu. Common

13:47 rabies, mumps, measles, covid. These are all kinds of

13:52 viruses. Okay so they're very um actually pretty common. Okay. Uh

14:00 the other prepared to point out is last one which is kind of a

14:06 don't know, maybe the opposite of retrovirus or it's a the variation of

14:12 called retrovirus. So it has an DNA genome that's cos the R.

14:18 . A. And then during the it's in its replication cycle to make

14:22 viruses, it will constantly reverse transcribed RNA back into D. N.

14:28 . Being accomplishments were put into the the partners. Right? So it's

14:36 1st, wow reverse transcribed harmony and D. N. A. For

14:41 purpose of having the genomes. so it's a demon virus.

14:45 And that's the way it makes copies its genome is just by this

14:51 Um Now the hepatitis B virus is one that's you're lucky you're familiar with

14:58 causes uh their disease can be quite . Yeah. So the viral life

15:11 . So we went through kind of generic life cycle at the start of

15:17 as part of the show you do . So there's many variations at different

15:25 in the process. Okay. Because was kind of somewhat really gonna rehash

15:30 that. So remember the post recognition tax. Right. So it's gonna

15:35 through the peripheral proteins. That's where obviously is on that uh that membrane

15:47 cash it envelope interface that um the of genome. So I mentioned before

15:56 there's variations, there can be the entire caption comes in to sell uh

16:04 continued to sell. There's variations. uh rotation of the genome. So

16:12 , the endgame here, right, what's coming which was infecting, here's

16:18 exiting. Okay, so the the does that requires requires lots of copies

16:24 genomes. Obviously I'm making it pretty diagram, everybody's showing you three,

16:30 know, a few handful of However sometimes it can be hundreds in

16:36 single cell. So um the uh of course the synthesis to produce

16:44 assemble everything And then eventually exit and infect more cells. Okay. And

16:52 uh the rate and we'll also see the rate at which this happens,

16:57 , is there 50 or 100 or of introducing themselves? It just isn't

17:01 really this five or six in Right. That that range of our

17:08 also takes a toll on the wholesale remember that all this stuff going on

17:14 sapping energy from wholesale. Okay. it's using wholesale nuclear tides, wholesale

17:22 many wholesale and enzymes and things and . So that's it's taken away from

17:27 host can be using on cortisone the is So how much is going on

17:33 in the replication of viruses will definitely the viability of the host cell.

17:41 and because there's viral types as we'll they can literally literally just do this

17:46 of rate of viral production. But with this these few viral progeny coming

17:52 at a time and that's something the can do the host cell can actually

17:56 along. Okay. Yeah and and the virus is doing this as well

18:03 it doesn't have to be it's not the case that whole virus infection.

18:07 we sell so they can die pretty . No that self can actually remain

18:12 for quite some time again. All on the viral type infecting it.

18:19 . So and they're expands the Okay they're different variations. Okay so

18:26 look at this question. So the part it's gonna be on bacteria

18:34 So uh said for the bacteria viruses their life cycle tends to be a

18:43 bit more less complicated than the animal for the fact that they're infected less

18:50 cells compared to ourselves. So we start off with looking at the model

18:56 the bacterial blocks. Okay. And it will have some have some features

19:05 are the animal viruses don't have but do have of course a lot of

19:10 in common. Uh Let's see. so take a look. Yeah so

19:41 talking about elliptic fage and Sophie ages whenever you see a page that refers

19:50 bacterial viruses? Always right. Okay there we go. 432.

20:21 . The majority says f who answered what are the what are the two

20:29 aren't part is like D. And . Correct yes. Okay so

20:38 E. Okay so um again terminology so always refers to bacterial viruses um

20:49 wouldn't use the term fade from an virus. Um One of the things

20:54 think pretty universal. I wanna say probably an exception out there is that

21:00 the bacterial viruses. Um Only the manners. So never the purple captured

21:08 of the virus. Only the Okay. Everything else stays outside.

21:14 Certainly many copies of phase DNA are . So the lighting face, let's

21:17 go into the differences between these So the lighting fage I figured as

21:24 end game is well any viral endgame produced lots of viruses and likely kill

21:31 . But for lighting virus that's that its goal. Okay. Hence the

21:35 lightened. All right we're going to in the cell but in the process

21:40 lots of fage. And so bacteria can produce of this type we call

21:45 even pages They can produce upwards of think 500 faith Purcell. Um Now

21:56 that overwhelms itself and the virus kills by a combination of the virus is

22:01 bursting out. But also they have enzyme it's called lifestyle design that can

22:07 down cell wall. Um Well look the cycle here in a second.

22:13 as with any viral type it's gonna this process of recognition binding and genome

22:19 . But with the bacteria virus this a type one of those tailed

22:24 Um It's called uh that the capsule here contain the genome. Okay.

22:32 it compresses within this part of the called the shaft is spraying and shoots

22:40 genome inside the cell. Um The cycle is all about uh in fact

22:47 Grayson Science cell began exploring that cell factory and then very quickly the selfies

22:54 then other cells are affected. So seen a small culture E coli line

23:02 dense lots of cell density in there then add a couple drops of the

23:07 in about 30 minutes. It looks water because the fates have basically affected

23:13 blown them up right. And all see is angry, so angry at

23:16 bottom. And the because they're all resulting in quick fashion. Okay.

23:24 that's your classic galactic virus. Unless any. Okay. Is a state

23:31 the virus can do what the virus . But it can also go into

23:36 state of inserting itself into the host and just kind of hangs out and

23:41 host cell just goes on its merry for a while. Okay. There's

23:46 a finite time to it because it last forever over the cell is unaffected

23:51 the virus that's inside of it. that's what we call a profile page

23:56 . So it will you can buy specific part of the chromosome and uh

24:03 hang out as a piece of N. A. Inside that

24:06 Okay. That's what we call a page. And so of course you

24:10 come out of that cycle and begin because that's it has to be.

24:15 the only way to do to make viruses is to come out of that

24:19 go into the lifecycle. Okay, those are components of estrogenic cycle and

24:25 called? Which is the which is dormant phase if you will of

24:33 And so it's always you know, are gene products produced while it's in

24:41 appropriate state that a lot of the had the health of the host

24:48 Okay, so it's all about that terms of what's it gonna do?

24:53 as a pro Pedro pop out and start feeding reproductive cycle. Okay,

24:59 let's look at it here. So terms um uh electric faget's age because

25:08 know, I have programmed to the that they basically make lots of viruses

25:12 then kill the cell. Okay, phages. Something's temperate. Right?

25:18 can kind of switch between moods, ? It can be mad and start

25:23 lighting cycle. Or you can kind just relax and just hang out in

25:26 chromosome while the cell is just functioning . Right? That's a temperate

25:31 Less estrogenic pages are that way. so so the first part of this

25:38 see the olympic cycle. And for lighter fage. This is all okay

25:47 life, afraid this is all it do is what you see here.

25:51 , so basically um it will enter cell. It will actually uh break

25:57 the whole chromosome. Right? And use those nucleotides for its own replication

26:04 the genome. Um it'll very quickly about proteins assemble and then put the

26:12 genome into the captain's as you see . Okay. And then as

26:17 this could be upwards of 200 and . That's a lot. Okay.

26:24 so that the combination of design life a greater released quantum effect multiple cells

26:33 course. Um and so so that's all of us. Just this

26:40 now, the land of age. . Can of course do that but

26:46 also do this. Which is a . Okay. And so um so

26:53 . So you see here and it a circular chromosome does lambda and it

26:59 insert. So it's it may not visible on your copy. But you

27:05 that there's a purple color purple. all these have a copy of what's

27:11 the Prophet. Okay. And as continues to grow from this war

27:16 And all those progeny bacteria will have copy of that. Okay. And

27:23 again it doesn't it doesn't have any effect on Jose in this state.

27:28 the profile profile state. So if multiply it well, don't grow.

27:34 then there'll be a point where that change. Okay. And um they

27:41 revert to the lighting cycle. Typically when that happens, the queue

27:47 that to happen is often when there's nutrients around and the Celtics growing quite

27:57 . Okay because in that condition that's of potential host cells for for

28:07 So okay let's let's start to break because these guys are really healthy and

28:14 well. So if I if I to the lighting cycle now, okay

28:20 I know I have a bunch of I can affect. Alright, contrast

28:25 , let's say a commission will host aren't growing. So um maybe kind

28:32 plateau just wrong very slowly then that's not a good opportunity for the stage

28:38 initiate the cycle throughout the paper because there may not be enough host or

28:44 to your economy. So really it's very often nutrition that triggers this.

28:52 do know that some stress is like think in the lab they can use

28:57 , elevated temperature to reduce as But often times in the natural world

29:05 it's often nutritional conditions of the host that that the state of or initiate

29:17 cycle. Okay, so um so like estrogenic stage have two options.

29:24 , but you know at some point some point it will engage in the

29:29 cycle. It will it will never just to make the pro face

29:34 Okay, it will at some point have to go like cycle too,

29:38 have to produce more problems. Um many questions. Okay so um

29:48 you have this going on your right? So this is the lander

29:52 uh is specific for control line? there's other similar types and other

29:58 But this actually goes on in the as well. And and when uh

30:04 uh those are the uh and then have a meal right? Comes

30:13 Right? That's actually opportunity. When see a lot of uh pro footage

30:18 out appropriate into the lifecycle. Because food now is a source where

30:24 lots of whole cells now let's let's it. Okay. Um, so

30:30 variation. Okay, so we saw . Thank you estrogenic page.

30:38 this is um A variation of Okay, so n 13 is one

30:46 will only produced fage at a low . Okay, so number one,

30:54 does not form does not does not a profit. Okay. It stays

31:00 external to the cell. So you it infecting here. So it stays

31:06 here. Okay. Outside the host , but will initiate replication.

31:15 so M 13 will form. And see there's a filament, this type

31:21 bacteriophage. Okay. And so, so, but the host, but

31:27 improves a lot. Doesn't prove a of is Okay, it's it's a

31:35 time. Right? The whole the generation time won't be where it would

31:40 if it weren't affected by the but it will be enough. It's

31:44 . So, it can continue Right. And it does. All

31:48 . So, what is the benefit that in 13 strategy? Why do

31:56 that way? There better not using the viruses, but yeah. Uh

32:05 , it would because it's producing less . Ah But what's that's not really

32:13 reason? What's the it's kind of on that track. But why why

32:20 this be a good strategy for 13? Yeah, bacteria provide some

32:25 for the virus. Yeah, almost around it. And yeah, the

32:35 is replicating because because it doesn't kill factory and there's always a host

32:42 Right? Yeah. That's right. always a host. So each generation

32:46 always always wholesale around to effect. ? So for a landing page maybe

32:53 . You know, it's it's so like a face can be really ah

32:58 was the population of course. But maybe a scenario I'm to kill themselves

33:04 that I have anything else with Uh But the other teams don't get

33:10 the same viral production. But you , it does have a host pretty

33:14 does have a host it can find it's exited. Right? So you

33:19 just how it's evolved. Right, little bit different. Um So the

33:29 we answered that um host defenses. one thing to always keep keep in

33:33 back of your head is um prior evolved we evolved obviously it's in response

33:43 . Okay. And uh there are books defenses. Right. So they

33:50 virus egalite stage um won't wipe out entire species. Okay. He tells

33:57 members among the population that will be to. Okay. So I mean

34:03 wouldn't um benefit the virus to obliterate . And um so they changed in

34:13 to each other. Okay so with course you're you've likely heard of restriction

34:21 you know they're used in the account D. N. A. And

34:25 jeans and whatnot. Um But of these are until we kind of exploited

34:31 for that purpose. They of course had an accident bacteria they were there

34:36 prevent viral infections. Okay so um and so this is an example of

34:44 such a restriction enzyme today in Ecuador which stands for e coli restriction in

34:50 one. Right? So they recognize kinds of sequences uh sequences.

34:58 And it will cut where you see slashes. So it'll make it cut

35:03 like that creating if you call the sticky ends. Okay. Like so

35:12 so this is a viral genome. they just chopping that viral genome up

35:18 um particularly for because it can ventilate to see your messages market and asterisk

35:28 . So it's D. N. . Is altered this way can affect

35:34 . But of course the virus viral wouldn't have that adjustment. So it's

35:41 . Okay. And there's literally thousands your future and enzymes each recognizing different

35:49 . Um I failed to mention uh here so you know in mutation

35:57 Yeah. The particular type of surface of the virus recognized and attached.

36:04 . Maybe these are protein in nature or glycoprotein and altering that sequence.

36:10 of course changed like changing the locks the billboard, right, It's gonna

36:15 uh unable to get exit. So that happened that that form of resistance

36:21 across all that have been America's Okay. Um crisper now restriction in

36:30 nucleus is to meyer. Now you're around bacteria. There may be some

36:36 trying to have those um chris You've probably heard it in a different

36:43 . Although it's it's it's a bacterial that was then of course it's what

36:48 used in and uh in medicine right to use that system to alternative and

36:58 sequences that that are in there uh may not function properly, leading to

37:06 types of genetic diseases. So we fix those sequences with the proper

37:11 then you can restore function and uh curing disease. So that's heavily in

37:18 and the work is being done with system and has been done for some

37:22 . And so um but looking back the bacterial viewpoint of what it does

37:28 you, it's kind of a pseudo was I immune system for the

37:34 Okay. Um and so the the CRISPR stands for only gonna say this

37:43 is clustered regularly, interspersed base for . And so what happens is let's

37:52 look at I have this diagram kind blown up and showing piecemeal here.

37:58 here comes a material fake. Okay know a virus and it will

38:06 And then the there's a protein called protein cast for short bacterial protein that

38:14 recognize the species uh part of the . N. A. And create

38:21 called a spacer. Okay so for sequence in this cut out will be

38:27 into what's called a crisper region. ? So this really is what the

38:35 the iron dome system has memory to . Right we can you can mount

38:41 in the response to infectious agents that the same comes back we can remember

38:47 infection and and uh the new responses vaccines are all about. Okay and

38:53 we have memory these cells that are that produce antibiotics in fact and so

39:00 in a similar fashion. Okay this segment of the viral DNA taken out

39:07 infection. It's kind of it's way remember bad virus man. Okay.

39:13 it's it's it's um lick to this . Right? Yes if it infects

39:24 . Right so that's kind of how basis for this mechanism. Okay so

39:30 spacer report Christopher region can be a of the collection of but it called

39:40 regions of different virus infections. Follows in the seconds are represent prior

39:51 infections because that's where they originally from . N. A. Of that

39:57 far as that in fact. And so how does how then does

40:02 come into play and stopping the Well what happens is that um when

40:08 viral infection occurs? In fact it transcribe that region. Okay. And

40:17 um process these CRISPR RNA is they're . Okay, into little segments.

40:24 . And so presumably one of these be one right that matches right?

40:33 will be homologous to the virus infected fact. And so it combines with

40:41 Cascade. 13 s. Okay. now in that combo looks for um

40:48 with the viral DNA. Yeah. so if there's a match, if

40:53 of these, one of these is match then it came by and inactivate

41:00 D. N. A. To break a talent together maybe and

41:06 prevent expression of viral genes. The is you can basically stop of our

41:12 at that point. Okay. But it depends on is there a is

41:17 a catalog of that stays in its region? Definitely the memory of it

41:24 you will. Okay. Obviously not about T cells and B cells and

41:29 likely will in our own system later . But it is uh it does

41:34 does represent a cannot previous infection. it is somewhat that they can use

41:41 to prevent actually the future. What's that? Mm hmm.

41:49 Is it similar to to eat Memory cells. I wouldn't go that

41:56 . It's pretty primitive but I mean it's um I mean there's no other

42:02 other than this CRISPR region and then ability to that plus the cast protein

42:08 become mobilized when this virus affected. but there's no I wouldn't say I

42:12 go that far. Okay. You a question. Yeah. Remember which

42:20 type is useful So I don't think that sophisticated but um certainly that.

42:33 I mean obviously that's part of the . N. A. And wanted

42:36 buy is gonna be passed on to product for sure. Um And any

42:42 that occurred prior to a divided that be passed on for sure. But

42:48 wouldn't go as far as you know . Exactly. It's certainly to a

42:54 immune system but it is for for it is. It's pretty remarkable in

42:58 way you know being just a lowly , right? It can actually do

43:01 stuff. Yeah. More. Yeah. Among other species. I

43:18 I'm not going to say that that impossible. But um I wouldn't put

43:29 out of the realm of other of bacterial species. Okay. Um we'll

43:35 about three about how that can be and whatnot the different mechanisms so certainly

43:42 can happen. It's it's in the ends up which will have any benefit

43:49 it because um if it's I'm not what the range post ranges and Orlando

43:57 it definitely affects ability to affect the for other stereotypes. I don't know

44:04 . So whatever species inherits that, much benefit it will gain depends on

44:11 is the same thing affected by similar as the. Oh jesus.

44:21 Um Okay so here this is our into uh animal viruses. Okay so

44:29 gonna leave bacteria viruses and go into viruses. Um Look at this.

44:36 let's recap what we have uh life . Um In fact take over the

44:45 replicate. Make lots of viruses and himself. Alright, um psychogenic stage

44:52 between cycle and that kind of born pro face state. The host cell

44:58 happy replicating in that pro fake statement like cycle at some point. That's

45:05 only way that buyers can make MIN 13 m. 13 sex.

45:13 But only because low levels of virus okay. And the host cell is

45:21 . Okay. Okay. So we about animal viruses. So bacteria viruses

45:31 they infected their hope there's really only really no destination. There can be

45:42 for analyzes. Alright. When they your periodic coast, right? The

45:49 between appropriate eukaryotic cells. Okay, um so let's see. 15 12

46:12 . Ok. Stragglers. Here we . 210 E. Overwhelmingly C.

46:23 . Let's see. Okay. Is D. N. A. Or

46:27 in it? That's really kind of can tell you what it will

46:33 Um Although there are even variations among as we'll see. Okay,

46:42 Alright, so um a virus life you can get a little more scary

46:46 you will. All right, so talking about tissue specificity. Okay,

46:55 is I think the cold virus binding a cells of the respiratory tract very

47:04 . You know, ourselves are often closely linked to each other. And

47:09 are one of those you might call adhesion type of molecules. And cold

47:14 can take advantage of that as part their entry mechanism. Um So they

47:21 the genome. Right? So the of course DNA viruses um typically although

47:28 there's always free to category there's always out liar. But for the most

47:33 , DNA bars tend to go to nucleus. Okay. When they enter

47:39 host. Okay, Well I just that. Okay. Why is there

47:46 tendency to go to this? Why you stay in the cytoplasm the house

47:53 defense? That was what uh maybe were you gonna say? Another

48:03 Okay, I can't answer a question a question. Is it? You're

48:14 ? You're getting there. Which is what what's that big? It's it's

48:24 acts on the chromosome. Right? . Uh No. You know,

48:29 it's it's ends and ace. that's where that's where that stuff.

48:40 that in high quantities and it's a . So, remember remember the nightmare

48:47 mitosis back in intra violates um is so I used to work for people

48:57 these kinds of questions. Sister or . Okay. Um Okay so remember

49:08 . Right. 20 eukaryotic cell divides you have the cell cycle, you

49:17 s fades, right? That's where the chromosomes are full of DNA

49:21 Right? So that's that's the Certainly for DNA virus to go

49:25 Although you do have some DNA viruses that carry their own getting memorized.

49:31 it's certainly not uncommon for me to there for that purpose. Right?

49:36 then weirdly you have RNA viruses, pretty much stay outside because then there's

49:43 need to go to this because you , you didn't ask liberates obviously.

49:48 but there is one that does But even just strictly on a few

49:54 , for example which is a I think anyway it actually goes it

50:03 has isn't nuclear part of the cycle some weird reason. So you typically

50:08 group where you do have a few and that's an oddball that will actually

50:14 some of its functions in. But aside from these outliers. Okay,

50:21 RNA viruses have have the DNA RNA RNA polymerase. Right, so they

50:28 to copy there are M. S into RNA molecules, we don't

50:32 that. Right. We have a . N. A. Uh produce

50:36 molecules were doing so from the N. A template. Okay.

50:41 of course viruses aren't doing that they're . Okay so uh retroviruses are very

50:50 this right? To copy their And so they were typed that very

50:59 analogous to a landing page. They integrate right? Like so much like

51:07 they can integrate their names too the . Right. And so too can

51:12 DNA viruses. Okay, so um uh let's look at entry.

51:23 open the sample box. Okay, this process encoding is what remember that

51:32 ammo virus you can have. Or it could be naked viruses

51:38 But you know, there's layers around genome and the is kind of what

51:44 of apart to release the free genome the cell. Okay, now the

51:52 process can happen on them sort of of membrane of the host or you

51:57 other nuclear membrane which which many DNA will do. Okay. Uh also

52:03 production of of vesicles in those Right? So recall um the processes

52:09 indo psychosis and exhaust psychosis. And eukaryotic cells viruses exploit that same

52:17 . Okay, So if we look um um encoding at the cell

52:24 Right, So right, the personnel sell and uh measles virus for

52:29 Remember there's always gonna be the Right? So this is a specific

52:34 with receptors the virus and the host then uh then the becomes engulfed,

52:44 ? Not engulfed rather it uh Right? Then bring fusion we call

52:49 in fact. So here's the Right? And so the envelope fuses

52:54 this because they're both living virus, ? The outlook of the virus and

52:59 cell membrane of the host cell. both lipid violators actually gonna meddle together

53:05 and now the capsule is released and and it combined with the license zone

53:11 something to break down that captured and genome. Okay, of course because

53:18 an RNA virus, right? This in the second outside of it.

53:23 that occurs here uh A I'm coding in those zones. Right? So

53:29 is what now we're gonna form. is not membrane fusion but we're gonna

53:35 a bicycle public. So um so of processes you can excel with that

53:41 things in through this process of receptor needed in the psychosis cholesterol is one

53:49 those molecules that will bind to specific . Get in gold and give them

53:54 himself. Okay. Um so of there's fire detection exploit the same

54:01 And so here's a hepatitis C virus again, always have that specificity

54:09 And then uh buy into the separate in the ozone formation then um in

54:16 case I'm actually confused with it, down the caps it and releasing the

54:21 . Okay, again, RNA viruses happening outside the nucleus. Right?

54:26 finally an example of one that actually into this damn virus. And again

54:33 there's one formation like finding the naked , like the protein spikes binding inducing

54:41 but doesn't release until we get to Okay, so again all mechanisms to

54:50 get that ultimately get the genome free then they can undergo replication or it

54:57 the time the integration of the host on. It can do that.

55:02 . So um and so we look a couple of other features you may

55:10 with antivirus. Is is this process ? Okay. Um this is kind

55:16 how an enveloped virus can acquire. all okay. This process of

55:22 And so the budding process uh there's that can be a current lola.

55:31 . And so you can have a viable host cell. What viruses are

55:36 college process? Cold shedding shedding Okay. Like a an animal is

55:49 its hair. Right. So it can be shedding viruses in this fashion

55:56 they eventually acquired a it's envelope and they go. And again it's not

56:02 high level of production. This whole was perfectly fine. Okay. It's

56:07 just probably finance part of growing as as it could. But it's it's

56:12 and um uh and but buyers have shaken from it. Okay. The

56:20 of viruses of course can occur. then they within the host cell processes

56:28 going to occur based on how you out those things. Right, So

56:32 have protein senses outside the nucleus and cytoplasm. Right, very often.

56:40 . Or just didn't sign is all And so the virus because it depends

56:47 hope follows the same rules. Like host is doing its bidding. So

56:53 proteins will be translated, produced outside . Okay, so and and so

57:03 some you'll have you have protein is made outside Memphis and then they come

57:09 into maybe a sample that comes Absolutely. So it's a little stressful

57:12 that's important here and there. depending on the viral type. Um

57:18 the Golgi is involved in the So the proteins are made in the

57:21 perhaps you go with them to the . They kind of assemble someone and

57:26 the viruses are produced and then they to themselves, so it's no it's

57:30 all the parts of the current self the eukaryotic cell it uses in the

57:35 of making stuff. Right. And that's why it can be can look

57:40 quite a complicated process because they're eukaryotic and that's the way things happen.

57:46 ? So um the so just once in the comparison between these two.

57:52 . And again, as I there's for both groups, there's always

57:56 few outliers that don't follow us but most do. Ok, so

58:02 DNA viruses gentrification and nucleus um because the process occurs outside and at

58:08 that's what it has to do. it comes back instantly to assemble so

58:14 largest can be a little bit uh because of that material passing back and

58:20 . Okay. RNA viruses basically they all their things outside the nucleus.

58:24 course. Okay. But again there's lot of don't do that like a

58:31 , so let's look at the DNA , papillomavirus. So this is a

58:38 that can cause cervical cancer women. um portrayal is a vaccine for it

58:45 quite effective. Um but it's one those that can actually integrate into the

58:52 chromosome as those types that can cause cancer of the forms of cancer associated

58:59 this type of virus. Um but with many I am a virus types

59:08 on what their host is. They tied their their reputation is tied to

59:18 the the functioning of that cell, that host cell operates. Right?

59:22 for example uh papillomavirus infects epithelial cells cells typically and they will. So

59:33 table cells are a type of these of these are ones that go through

59:37 cycle of differentiation. Right? So cells are the form that is really

59:45 a growing for. Okay, the forms are the size. Alright,

59:53 going from left to right, like looking at a thickness of these types

59:58 ever getting cells. Okay. And basal cells in the florida masks are

60:03 that aren't really grown. Okay. as chemical signals come down than some

60:09 those differentiates. So we're going out left to right, differentiate eventually into

60:16 . No sites which are very rapidly cells. Okay, so quite a

60:21 to you, basal cell is not that would differentiate in the Okay.

60:29 so the coronavirus then it's one of gratification is tied to that.

60:38 so if the cells are growing very some they're just kind of sitting there

60:44 for the signal to differentiate um papilloma that affects those. It's just kind

60:51 sitting around. And so for a of those, that's where they may

60:58 . All right, so the people our DNA integrates into the whole

61:02 Okay. And that and it's in basal cells that can count. In

61:08 um now here we all are, cells are basically don't pay attention to

61:15 usual rules of cell growth control. all controlled representative control growth because when

61:23 insert themselves can be in a critical of that chromosomes had control. Um

61:32 okay, so um and so those that can potentially form cancer cells.

61:40 . Um as we get to but as they differentiate into the faster growing

61:45 types then uh so remember, you , as the rose replicates,

61:53 That's then, you know, that's racer in the nucleus. Right?

61:57 that's when the papilloma virus will begin well and you see them being produced

62:03 being released. So um so again their life cycle is tied to kind

62:10 the cell types a defect and the of themselves. Right. That dictates

62:16 how much to buy raffle then Okay. Um and so we're just

62:21 of a simple diagram showing kind of life cycle. And so this is

62:29 a double stranded DNA virus. So a DNA virus, it's one of

62:33 that doesn't go to the nucleus. unquote at the nucleus I should

62:40 And then uses hosting. Okay. the you know, so so tied

62:47 to the whole cell replication rate. that determines how much of this the

62:52 is actually around. Okay. And um so again you have uh production

62:59 child cooking outside because that's you that's how it works. And you

63:02 itself and then material travels back into assembly occurs and then exit.

63:08 so um it's a and it can this. Right, wow. And

63:15 the cell can actually rearrange so much . It all depends on how much

63:19 being produced. Okay, so you the term sharing, So sharing

63:25 Okay. Um Okay. Any questions it? Okay, so okay,

63:33 here's a question. All right, goes now we're now we're going into

63:37 RNA viruses and the plus minus Okay, so um so a hypothetical

63:46 . This is just a really basic . Okay, so hypothetical minus single

63:55 RNA viruses. 10 rabbit nuclear times . Okay. Which one below is

64:01 likely gets genome. Okay, so about what the minus RNA represents and

64:10 you could or could not do with . Okay now hopefully we can eliminate

64:17 of these answers right off the bat you if you don't know.

64:25 Mhm. So I assumed you remember of the old intra vile protein synthesis

64:57 . Okay. Excuse me. it's a minus. Right. So

65:31 said you have to hearken back to and high protein synthesis works and

65:40 Maybe you don't remember. That's Well, it's not all right.

65:52 With that one. Okay. Okay. Okay. 765 21.

66:24 at that. Okay. Okay. about right. All right. Um

66:34 , good thing. Good news is eliminated. B. Why can't it

66:39 B. B. S. N. A. Right.

66:43 You got timings there? So remember so he's out. Okay. So

66:52 minus RNA strand is um is that template to make a polyp peptide?

67:03 hmm. The minus strand Barnabe the to make a protein? No.

67:14 . So based on that knowledge, did you think? Mhm. After

67:23 he just responded to me. Okay. Alright. So you are

67:35 . What's happening in music? One. Yes. Mhm.

67:46 What? 16. Thank you. . So because Okay, so a

67:52 of things you write his own your zone will read And are in a

68:00 5 to 3:00. Okay. And remember the punctuation marks of a

68:07 Right. So you have a G. C. U.

68:11 All right. So um so the the minus R. N.

68:20 Have those elements minus RNA heavy Because if it had a G.

68:29 that mean it can be on it start like in Turkey. So see

68:39 what type of already So remember there two mice plus write A plus is

68:50 . R. A. A plus on the theoretical started improving. So

68:57 that yes, the type of RNA that the cluster minus would be what

69:05 is what he made directly translated into . Okay. So we always said

69:11 DNA. So that's plus string. . So as you said Au

69:19 Right. Start code on and this one and grant this is a super

69:26 , you know, sequence, you ? But but that's A G.

69:32 right. That's that's the template for . But that's the definition of a

69:37 strain. Okay, so by That's the antisense script. Okay.

69:47 Zach have insane. Right. So so you know, you took by

70:01 one that was a pre right? brush up on your so I'm not

70:11 have you solved. But let me blasted. What's the what's the problem

70:17 ? But because I expected to know any questions about for that explanation.

70:26 , it could be that they were yeah, a lot of your problems

70:36 this that they trained. They always it started at the very beginning.

70:39 not reality. The can be several because there's other elements needed by his

70:46 binding site and that kind of So. All right. So um

70:52 hmm. Just went through that. , so here's the question about uh

71:03 army Flynn raise enzyme is not needed a what? Mm hmm.

71:38 Okay. This spell R. B. R. D.

71:46 P. Sure. And I'll give a hint. It's not E It's

72:20 E as an eagle. Okay. as an eagle. That is not

72:25 . It is a It is a . Um Okay, let's um So

72:41 as a uh remember reminder your templates translations right through RNA virus Jack.

72:54 can be a template for to uh a protein for translation. It can

73:01 attempted to make a transcript. It be a template to make D.

73:05 . A. Retrovirus. Okay, uh let's just look at that.

73:14 is one of the two cycles of plus and minus. Once again.

73:19 so and your plus are angry, Nile poliovirus, police monitors. Uh

73:26 I started like this just to remind me uh here's what the Endgame

73:30 . Right? This is what we're to. We have to make viral

73:35 right? That have a plus genome it. Okay, so of course

73:40 the box hexagon around it represents, know, and whatever other proteins.

73:46 ? So viral proteins and copies of . Alright, so you start with

73:53 right to make um to make uh to make copies. Right. So

74:02 gonna make lots of So again, , it's a numbers game to

74:05 the virus infected with this plus But you also want to make lots

74:12 stuff. Right? And you have make lots of copies of genome because

74:16 gonna have to mention put Right, let's do it this way first.

74:22 . And again, it's just the frame rules. We're gonna make a

74:28 Now. Let's see. We're building lots of lots of stuff.

74:33 So all those virus wants to be into plus strings. Okay. Which

74:38 a lot of protein sentences that can very quickly as well as making all

74:44 cottons of gino. Okay, so what then happens, translates something that

74:54 packaging department. Okay, so that's cycle of Okay, so remember,

74:59 all down quantities of stuff. We need lots of stuff to make

75:04 of stuff. And so and and of copies of genomes. Okay.

75:11 this wrapped. Okay, again, the endgame, Right, So,

75:18 going to have to make certainly make of the plus. That's R.

75:23 . R. Is going to have make proteins can't make proteins for a

75:27 template. So make lots of plus then that makes lots of viral

75:33 But then all those copies can be into the genome. The former

75:39 right? The minus strands like. . Right. And then package So

75:46 uh so that's why I always harp what what is down here. What

75:53 the project is supposed to look And you have to make what they

75:56 right, in this case minus RNA and of course all the vital

76:02 Right? So And you can It only ever works plus to -12-plus

76:08 just tied to that room. It's not a rule because we're talking

76:14 viruses there's a rule because we're talking the Okay so um so ruminate.

76:25 on this. Okay. And uh have retroviruses do. We'll talk about

76:31 next time. Alright, so thanks . See you thursday. What's going

77:24 ? So for example when when your own DNA gene expression. Right?

77:31 you're like like everything else your DNA . So you want to make a

77:40 of your going to make a copy that. Plus drink that contains.

77:46 way that happens is by copying the strings. So what you're essentially doing

77:52 to make a copy of that minus strands plus R. N.

77:55 And that's what goes to the US go to the ones that are sitting

78:01 the er protein. So we don't we do not we do not we

78:11 make minus RNA because we have no for those. Right? Because because

78:15 never copy plus RNA and anything viruses RNA viruses do. So that's why

78:22 why the RNA dependent RNA polymerase is found in eukaryotic cells because we don't

78:28 that process, we don't have no for the minus. So yeah,

78:34 have another

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