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00:02 Yeah. Okay. Mm hmm. folks, let's get started.

00:26 so a couple of things uh Windows open tomorrow so that will be a

00:31 more comprehensive. Um the uh it's smart work, remember that's due this

00:40 on sunday and Tuesday and cost exams week? So you're four for material

00:47 start on Wednesday of next week. that that is already up. Everything

00:52 there that you need ready to Okay. So that is the uh

00:57 the hell there's technically a final exam is not, its only his exam

01:03 , it covers uniform material. It's comprehensive. Okay, so the,

01:11 today we are going to get through , I'm not going to do all

01:17 the remaining traffic tennis that we're gonna through here this slide and we're

01:22 we're gonna talk about these topics next and then that will close out uh

01:28 three, chapter 10. And then the end of in terms of what's

01:33 the exam. Okay. So uh what we're gonna do is go through

01:41 really the rest of chapter this chapter part one. So we have yet

01:45 cover the fan Opteron and there's a of the control of the opera on

01:49 that's kind of pushed into part two this Chapter 10 material and and we'll

01:54 that. So basically just we'll do little bit of rehash on some of

01:58 stuff we've been talking about in this and then um and then finished out

02:05 trip defend Oberon and all the control goes on with that and then we'll

02:10 it a day. So uh sober uh didn't want that one to pop

02:17 . Let's go to this one. so eyes over here first. Okay

02:21 remember that uh kind of uh yes concept here. Right so we're looking

02:28 controlling gene expression. Okay so we previously previously went through operation structure.

02:33 we're coming back and revisiting it and how genes are controlled. Um and

02:39 the levels of control. So remember how genes are expressed right from

02:45 translation. Obviously this is where the points are as well. Okay so

02:50 can control we can manipulate DNA sequences nucleotides and that can influence expression.

02:56 can uh determine whether or not there any preliminaries will transcribe or not transcription

03:04 control. Very common mechanism and Um if the transcript is made then

03:10 can still have control there. We influence how stable it is, how

03:13 it hangs around. Um We can translation and manipulate the river zone or

03:20 going to translate or not. So control. Uh and then finally the

03:25 product of proteins themselves can also be whether through enzymes that are producing them

03:34 through ah modifying proteins. The typical too far forward. The protein that

03:41 kind of activate or inactivate. Uh depending on the protein. We can

03:46 just get rid of it completely. the point is any of these things

03:51 happen to control gene expression and they can all occur in combinations as

03:58 Okay, so all the efforts keeping control on really the functions of the

04:04 . Right? Because of course the being expressed or functioning in some sort

04:08 cell something doing something for the cell some way. So obviously the needs

04:14 a cell change. Microbial change certainly be rapidly. Maybe not so much

04:20 make what the environment it's in but gonna have a tight ring on all

04:25 functions and does so through not controlling points. Okay. Uh we're really

04:32 look at some of those different We're just focused now on the opera

04:36 the model and how the whole things through the through this probably talked about

04:41 one before. Uh these these people here. Right, induction de

04:46 So these terms you see here and , next week we'll look at some

04:51 examples of things other than just kind just operate control but for now we'll

04:55 focus here. So remember last time gonna be some again some terminology to

05:01 with the expression control. So, deeper pressure on me that that serves

05:07 uh these mechanisms turn on expression. , repression may often involve a co

05:14 that is about minimizing or stopping gene . Okay, and so this is

05:21 definition active versus inactive repressor. So involving they're ready to put the protein

05:27 compressor. That as we saw last relax those opera acts with the operator

05:33 . Right? That whether it's active inactive, that definition doesn't change.

05:39 what can change is one of the that bring it about and we'll see

05:44 these are two very opposite conditions um pressure from here combined to the operator

05:53 whatever the regulatory sequences. And then that would act as a block to

05:57 proliferation from terrance Bryant. Okay, we acted with pressure requires a co

06:03 . Right? So together, only they're together can they buy the operators

06:08 expression. So again the different. , but an active active repressor here

06:16 here. Right uh yields the same . Right, So active and active

06:25 the same results stop expression but occur different ways. Okay, similarly to

06:30 them, Same thing a little bit . Okay, and so the inactive

06:37 is generated through the the top top through the inducer and do certain induces

06:46 . Right? So it binds the and then that eliminates expression. And

06:52 down here in the irrepressible opera the is united by the lack of the

06:59 oppressor but it goes away. That's uh induces de repression or expression of

07:06 gene. Okay, so kind of know, you should be comfortable with

07:10 terms and what they mean. And versus inactive oppressor. Um and then

07:16 course on top of that we can have or in addition to that,

07:20 not just not just relieving the whatever the mechanism is, you can

07:27 add the function of activators. So will enhance expression. Okay, you

07:33 think of it as these two mechanisms inactivate the repressor allow expression to

07:40 Okay, that can sometimes be different increasing expression. Right? So we

07:46 allow it by one of these Okay, but then we can really

07:51 it by involving an activator. that's kind of how that it all

07:55 together. Okay. And so inactive increasing expression. Remember, it's kind

08:01 events happening at the promoting right molecules together. Activators. And depending on

08:09 organism in the scenario, other molecules come together at the promoter. It's

08:15 about enhancing the affinity of the promoter to the preliminaries to make those two

08:22 together. And so if they do in a very kind of tight

08:28 if you will you get lots of . Okay, so that's kind of

08:30 activators Rolls of those things are. . Um and so, you

08:36 an activator is not necessarily going to , right? Unless this has happened

08:41 the repression has been inactivated. So now there's access to that promoter and

08:46 when the activators and things can come . Okay, so uh that's kind

08:52 the nuts and bolts who went what went through last time in terms of

08:56 there any kind of questions about Okay, so uh I think one

09:01 that if you're kind of still fuzzy it. One thing that can help

09:07 take a look at a couple of animations and these are available call on

09:12 blackboard site, there's a on the , there's a menu button there that

09:18 take you to the textbook publisher material in their animations. And this

09:23 this is from that. Alright, there's one of the laptop round trip

09:26 opera on and you can you can on enable the text too if you

09:31 . But let's just kind of take look at this one real quick to

09:36 black cop Ron. Okay, and I'm gonna kind of just just goes

09:42 little slow. So I kind of to hurry it up a little

09:44 So here's the lack off run in to say E. Coli and uh

09:49 course remember the three genes. So don't have to worry about the lack

09:53 right that transit satellites, there's really knowing what the exact we know it

09:58 something to do with lactose metabolism. uh so just worry worrying about Z

10:03 Y. And so the um and here's a scenario we have glucose um

10:14 remember uh a couple of factors Right, so the presence of glucose

10:19 the influence, it has an expression course having the president's having lactose President

10:24 course is necessary for the upright to expressed. There's no need to express

10:28 , if there's no lactose around. so then remember the influence of the

10:34 white product is lactose permeates. This the thing that allows you to basically

10:38 transport protein for lactose specific proactive and will enable to sell. It's the

10:43 the soul can quote see if there's out there. Okay, so in

10:48 present scenario we the blue dots are glucose. Okay. No lactose present

10:55 . Okay. And so but again we have a tiny tiny low level

11:01 expression. Okay. And um and need that in order to form the

11:06 permits. And again, it's we're talking about a couple of molecules

11:11 Okay, so here is um because like coast. Alright. That's going

11:18 because repression no expression of genius. . And so um so for

11:29 Okay, so here's our like There's the regulatory genes like i that

11:37 for the repressor. Okay. And that forms a te trimmer.

11:45 And the te trimmer will bind both operator of the lack of opera and

11:52 the black eye. Okay. And what brings about this um coming together

12:00 the segments they're hiding the promoter So that our you know, primaries

12:07 really do anything. Okay, promoter not accessible. So um so of

12:13 that scenario occurs certainly we're not going be close as present. Okay.

12:20 and even if that person is present not. Right, so now there

12:27 occurrences, right, normally this is state. Right? But there's

12:32 you know, occasional rare time. back up a second. I win

12:42 that uh come on like more. , so here so okay, like

12:51 said occasionally there'll be a time when can sneak in and make it over

12:55 transcript, even though it's repressed because this binding is not irreversible, it's

13:01 bound but there's a little bit of when it's not and that's when they

13:04 sneak in and make a little bit transcript. Okay, and again,

13:08 importance is to make the permits. , so black president buy into

13:13 bring it in. Okay, assuming there is no glucose present and then

13:19 break it down into the dissect Sacha rides checking in going to metabolism

13:24 little bit of it goes to make low lactose time. And so ella

13:31 is actually the inducer. Ok. you see here. Alright, and

13:37 um uh so here is in the form of the oppressor, right?

13:43 have an inducer bound to it. in the state it can't bind to

13:47 operator here, I'm sorry here, it's a present because absent michael's present

13:54 . Okay, induction. And then we have the contribution then of the

14:05 mp. Right second MPO levels rise the absence of glucose and now available

14:11 bind to the receptor protein and form active activator form complex. Okay.

14:18 that promotes lots of binding by political to to um promote expression.

14:25 but when glucose is present then that imperial was dropped and now you can't

14:31 that um ah activator complex. so again glucose you want high level

14:39 expression of lactose flaperon. Get rid glucose obviously have lactose there.

14:45 Um so the uh um let's get of this one and we'll go just

14:56 this one up for in a few . We'll look at this one.

15:01 , but any any questions like what's ? Okay, so um so as

15:11 go into the we just went through that. So let's look at this

15:15 . Okay, so it's our segue the tryptophan opera on. Okay,

15:21 which is true regarding the trip to opera. Okay. Uh The operating

15:27 the metabolic pathway for metabolism. A to fan be in the absence of

15:32 co repressor. Fan operation will not expressed. The repression occurs when the

15:40 presents two different co repressor is trip fan itself. Well, none of

15:47 are true. Mhm. Okay. , let's go through these.

16:39 so first off defending controls. It's pathway that is for the synthesis.

16:48 metabolism. Alright, lactose up. is good. Catapult pathway uh for

16:55 breakdown and of lactose for as an source, this is all about

17:01 Okay, in the absence of the pressure. Um the trip different opera

17:07 not be expressed that actually it will will be expressed okay in the absence

17:15 the covert pressure as we'll see here a second the repression so remember that

17:19 is to stop expression. The repression the opposite. So that expression.

17:25 and so that occurs when the fan absent. Sure. And then uh

17:33 incorrect statement is d okay, tryptophan repressor is actually it is for the

17:37 itself which is kind of a self process. Check. Um so let's

17:44 at that here. Okay so again trip opteron right, is here's your

17:53 operator. Typical opera in structure multiple these all code for different enzymes of

18:02 pathway to make tryptophan from his starting called charisma. It's okay. Um

18:12 the tryptophan synthesized then of course can used primarily for protein synthesis.

18:18 All the all of the amino acid pretty much work the same way.

18:24 controlled the same way. Okay um so the in this situation where that's

18:33 reiterate. So back up a So the trip are is the regulatory

18:37 . Okay so the papal repressor is form that is not activated, dresses

18:45 inactive form here. Okay um and in that form it can't bite.

18:53 to the operator. So you can bind, become active when tryptophan binds

18:58 it. Okay so that if the present or low tryptophan then you get

19:06 because then the operator is not bound the oppressor and you is for you

19:11 transcribe. Okay. But if trip fan accumulates okay now it is free

19:19 bind repressor and activate it. And so um and so hence it

19:28 a core pressure for that reason binding the pressure makes the active complex.

19:34 um and so it binds the operator then we block expression. Okay so

19:42 couple of things. One is when tryptophan actually be present? Wild guess

19:50 would in this cell when is going accumulate? When is it not going

19:57 be used? It was being made not going anywhere. When likely would

20:00 happen? It depends the meal acid to make proteins. If those are

20:05 sitting there going no where where is most likely to happen? Doctor give

20:11 something, throw something at me. myself was like what should defend be

20:21 for actively growing. Wouldn't wouldn't that used for tryptophan if it's actively grown

20:27 proteins? Yes yes when it's the just slowing down or maybe you've zapped

20:34 with UV light. Right and all a sudden it's stressed right now it's

20:39 certainly not going to be in the to make sure you put the fan

20:42 make any protein proteins. Right remember thousands of proteins. And they sell

20:50 bet the farm that each one of proteins has at least one trip to

20:53 . Right? So the cells actively trip making proteins, it absolutely will

20:58 using tryptophan among the other As well the other 19 amino acids. So

21:05 one growth when it's when it's growing gangbusters, it's a log phase growth

21:11 what have you. It's it's basically using as fast as it's made more

21:16 . So interest several levels will be low when it's actively growing. But

21:22 , it's not an all or It's going to be a continuum.

21:26 . It could be there's almost Okay. If it's a super stressed

21:32 , maybe it's a late stationary phase something, you know? But but

21:39 could be, you know in maybe maybe before mid log phase maybe at

21:44 beyond. But it's gonna fluctuate. going to be in a state of

21:49 there's a little and a lot or lot and a little. Alright,

21:53 depends and it will adjust accordingly. but the point is that again,

21:58 will not build up in a cell something's happened to that cell either nutritionally

22:04 grow much anymore or it's stressed in other way that's when you should defend

22:09 made previously will then accumulate. So signal them for themselves. And that's

22:15 not keep making more trips to fan do that? Because I'm obviously stressed

22:20 something is stopping my growth. I need it as much anymore. So

22:25 again, as I said, the time this semester processes like this gene

22:34 DNA replication protein things all take lots energy. Okay. It's not obvious

22:41 it's not showing you a tps being or whatever, but it takes a

22:44 of energy to do this. So you're gonna definitely keep it under

22:49 . So I want you to see on the screen does control probably 95%

22:58 the expression. Um But so there a plan B. Okay for a

23:07 bit of expression that may occur when doesn't put the complete clamp on.

23:12 , so in other words, in state here. Okay, repressed.

23:18 , that again this binding. That binding is not irreversible. Like

23:24 can come off and it may do well once in a blue moon.

23:28 ? Not a lot. But it . And that's the opportunity when you

23:33 you can transcribe this. Right? so you kind of want to if

23:40 need to you want to keep that to zero as close as you can

23:43 the situation requires that you like. , so again, whereas most of

23:48 control is through this mechanism, you a backup plan in case.

23:54 and that's what involves this sequence. you notice that when transcription occurs,

23:59 get this obviously these are the structural . Okay, but you also get

24:05 because that's actually right before. I this was right before that information,

24:10 leader sequence. Okay, so and really the can be control mechanism.

24:16 gonna talk about next the attenuation So if you do that a little

24:22 of expression when you don't want how can you still put a clamp

24:26 ? And that's what are expected to which structural genes are involved in a

24:32 between. Absolutely not. Yeah So um uh yeah he was responsible

24:42 knowing the control mechanism. That's it just as a repressor. And if

24:46 don't need it yeah as long as can you know well you need to

24:54 the unit quiz. So if I something what if what if there's a

24:59 that the repressor doesn't mind anymore. things like that. Right so you

25:06 it off and I'm not saying something . But no it you know what

25:09 mean? Right so but there will questions like that on the quiz.

25:14 think of okay if this went wrong would happen? Okay that tests your

25:20 of the mechanism. Okay so so said can you get a little bit

25:27 expression when the soul doesn't want The first thing that gets transcribed is

25:32 leader sequence and that's really the crux the whole attenuation mechanism. So let's

25:37 at that here. Well not I forgot I wanted to throw this

25:42 first. So again this is about able to compare and contrast between the

25:47 and left hop around. We just about. Okay so here we have

25:51 . Coli which which can has lactose on as you can see lack plus

26:00 a trip Oberon. So obviously you ferment lactose you can use like toast

26:05 metabolize it. It can make a to France because of that. So

26:08 growing on minimal medium. Okay containing lactose and tryptophan check. So no

26:16 coaches present. Okay so what can say about these cells with respect to

26:23 and trip operations respectively? Okay so for lack opteron in this scenario is

26:31 opteron expressed yes or no. Yeah. Yeah because lactose is

26:40 glucose is not. That's the clue key. Um Is the trip Opera

26:46 expressed? Why not? Obviously trips already. Okay um What is the

26:55 of the oppressor in Black Opera is active or inactive ah inactive. Right

27:05 inactive repressor allows expression. Active repressor not it stops expression. Okay and

27:14 means it's not working. Yeah Exactly. Exactly. Um So trip

27:20 is an active or inactive. That's . Sorry you're right. Alright so

27:28 to fan if the court pressure so bind third pressure and inactivated. Okay

27:33 activated. Sorry? Co repressor binds the pressure and activates it. So

27:39 have an active with pressure. Okay binds repressor but does not prevent the

27:46 from binding to the opera. No the thing. It's opposite. I'll

27:51 lactose and I just offering. That's . And if you're different operators not

27:57 binding to the repressor activates it binding the molecule and the black opera an

28:05 . So correct. Yeah. Yeah that's that's the the term active inactive

28:16 means the same thing in both It's what is causing it is way

28:20 . Right? Um so second GMP are the higher road in the lack

28:27 operation scenario. Uh Yeah, so will lower it. So no glucose

28:34 . Doesn't apply it. Obviously the opera. Okay. Um Okay so

28:40 the so this is the um plan . Control for the trip operation.

28:47 again, mhm 90-plus% of it is care of by the previous mechanism.

28:54 takes cover a little bit that that's . Okay, so again it's all

28:58 around this leader sequence. Right, it's called. And so I'm kind

29:03 doing a little different here because I to show I'm going to show.

29:08 this Alright, so this leader Right. This is the trip.

29:16 . Okay. Leader a couple of . Note the location. Right

29:24 Right here. So these are the jeans the beginning. Right? It's

29:33 E D C. B. Okay, structural genes are this way

29:40 that point. So the mechanism is , is about really are we going

29:46 allow RNA polymerase? Which is right . Right. So here's our nina

29:50 race. Mm hmm. And Okay, so it's gonna go It's

30:04 Transcribed that trip leader sequence 1st. changed my pants color here. She

30:11 the leader sequence. Right. And here comes our people embrace. All

30:18 . It's moved from here down here as it's transcribing. And here is

30:27 on a on a form of the sequence. Okay, just basically transcribing

30:37 DNA making the art form. And so um and so here's our

30:43 down here now. So it's about that going to continue to go forward

30:50 is it gonna be knocked off? that's that's the all or nothing

30:55 Okay. So if it's allowed to then it will transcribe the structural

31:00 If not it gets knocked off then won't. And that's that walnut shell

31:04 the mechanism. Okay. Now, determines whether it gets knocked off or

31:10 ? Okay, well that involves these . Okay, so um we have

31:19 adjacent trip coordinates. Okay, right . Oops. Two. Okay,

31:32 we have a normal Mhm Stop cooking all transcripts we have. Okay,

31:42 right. So, um now the zone. Okay, will bind.

31:52 here is our right, okay. so it will move forward once the

32:05 begins to be made. Um So mechanism of whether it knocks off or

32:16 is about the position of the river . Right, Where is it going

32:20 stop? Is it going to stop for here. Okay. Two

32:31 Right? Starting stop at that point that Right. So it's really whether

32:42 knocked off or not, it's really it's it's a mechanism where it's transcription

32:46 control. Okay. Because we're influencing the audience criminals can transcribe it.

32:54 the definition of transcription control. What's but what's actually kind of controlling

33:01 temperature control is the ribosomes. That's very kind of very legal.

33:07 but most of the specifically it's the of the river zone. Right?

33:12 so if it stops here at the code ons then you get the army

33:20 gets to go and keep transcribing. , if it stops here at the

33:25 code on then it won't, it off the. Okay. And that

33:32 happens because there's secondary structure with this this particular transcript. Okay, there's

33:39 that will it will fold up. , so now let's flip to the

33:44 thing. So another thing before I to the next five. So what

33:49 whether it stops at the trip code or the stop code on is what

33:55 required for translation? Are these Right. I draw them like

34:01 Right. Uh And this will have anti code on corresponding to the code

34:09 the T. R. N. . Right? The charged P.

34:14 . N. A. S. ? So this will contain the anti

34:18 on. Right? That's charged. means the Trn A Right? Charge

34:29 N. A. Has its its acid hooked to it. Right?

34:34 every T. R. A. specific for each coat on,

34:38 And that is bound to a one the 20 amino acids. Okay.

34:42 makes it charged when it's hooked hooked it. Right? Uncharged. Would

34:48 like this. There's there's nothing. right, that's uncharged. And so

34:56 charges uncharged. And so then what that? All right, Whether you

35:02 a trip to fan residue there or . Alright. It's black, it's

35:10 . Right? So the level of defending itself determines that. So,

35:17 you have a lot of trip to in the cell accumulating, then you've

35:21 lots of this. Okay. Which that the survival rate is going down

35:27 transcript. It gets those trip cordons won't be any hesitation. Will just

35:33 right through it because you've got lots charge. Trip to RNA is

35:39 And they will go bam right in and it'll just keep going. So

35:44 scenario, that's when it will stop the stop code? Right? In

35:49 other scenario, if you have lower trip to fan, then you've got

35:53 of many more of these. And then it gets to the trip

35:57 ons and it's gone, oh, can't go any further because I've got

36:02 uncharged T. RNA. Is sitting and they can't form a peptide bond

36:08 there's no amino acids there. So just stalls, right? And so

36:13 it's position there means the that the can actually go unhindered. And so

36:22 just let's look at that here. So what you have on hand as

36:29 ? Okay. Are these labeled Right. Our regions of but but

36:39 strand can base pair with itself. it's all a Ugc. Right?

36:44 all it is. Right A's B's with us. Right. G.

36:50 . Right? So there's lots of compatible sequences in those regions that allow

36:56 to Buy them together like that. and so it's all thermodynamics.

37:03 And the ones that form are likely that are having lots of a.

37:07 right away. You have only 200 bonds G. CSF three. So

37:12 going to be energetically more favorable to together the AU sequences. And so

37:17 23. Yeah you can actually form . Okay and that is the one

37:25 will for most of the time. that's the one that's most energetically

37:30 So it's really a battle between that's called excuse me. That's actually called

37:37 anti attenuate. Er the 23. that one And so it's a battle

37:48 that one in that one the continue and the anti attenuated which one will

37:55 . Okay and so that again depends where is the ribosomes sitting? Where

38:00 it stall at the trip protons are the stop code on that determines which

38:05 forms. Okay so but again it each thing leads to another. So

38:11 all goes back to one of the of tryptophan. That determines the proportions

38:16 these. Okay, that determines where privacy almost stopped. Okay? And

38:22 that determines which loop forms. And then that determines whether preliminaries can

38:28 transcribing or get knocked off, So it's one leads to the

38:33 Okay? And so um so let's at the high tryptophan scenario. Okay

38:41 high tryptophan, you're gonna have lots these is you're charged trip Tr

38:45 S. Okay? Um arched. and so um so it will go

38:56 the stop code on the regular, stop code on. Okay. And

39:01 that you see here is a regional and two. Okay so the ribosomes

39:10 that up physically covering it up. so that promotes the formation of The

39:17 4. Okay and so notice the two, the rhyme zone is traveling

39:25 . Remember like we have we have we have a primary zone is I'm

39:30 excuse me memorizes going ahead transcribing And so the 34 loop is in

39:37 proximity to it. Okay and that's the contacts and actually knocked it

39:44 Okay so second story structure that forms actually the obstacle that interferes with the

39:48 rice and goes away. Okay And again all based on. Okay,

39:55 tryptophan levels. Alright, high level charge tr N. A.

40:01 This will mean that a person can past the trip code on center together

40:05 stop the stop code on that covers the region here. The three or

40:10 conform. The antibiotic will be continually then. Okay and so we prevent

40:17 of the structural genes. Okay so the low defense scenario we have more

40:25 these. Okay Which means as it to the trip cardin's it's going to

40:31 it can't it can't make the bond the peptide chain so it just kind

40:37 stops there. And so of course only covering up that's that's really at

40:43 beginning of the transcript. And so two adjacent trip code on. So

40:48 only covering up region one. That's region one right there. And

40:53 now two and three Or free to even though four Is available to bind

40:59 3. 2 and three is more favorable. Okay and so it will

41:05 will favor that loop, hairpin loop and so then you can see compared

41:12 the distance between that and the That's up ahead. Okay so comparing

41:21 here in here. Okay you can't with it basically. So the plane

41:28 is free to keep going. Okay is what you want because you're low

41:34 to fan and um uh you are to maintain uh transcription to keep making

41:43 of it. Okay so um that's this works. So it's kind of

41:51 it's all about RNA positioning. I'm ride his own positioning on that leader

41:56 . Okay. And that's influenced by of crypto fan because that determines the

42:01 of charge which is uncharged TR A. S. Which will determine

42:05 it stops or stalls. The trip are at the start. That then

42:11 what do forms the attenuated or anti . So kind of, It's like

42:16 story. That thing one happens in in a row. So um and

42:23 just start with am I in the or low trick defend mode? Then

42:28 will happen after that? Okay. so let's look at the next um

42:37 we go. Animation. Yeah, ahead. You have a question.

42:43 . Everything gonna show us the Exactly. I think so.

42:48 it will. So let's see Okay, so again, here's our

42:57 opteron mm hmm. Starch. so I'm gonna we have some stuff

43:07 . Again, some structural genes, regulatory region. There's a transcript until

43:13 products of the transcript form or what of the pathway to make crypto fan

43:19 um such a defendant's produced green And then um there is a

43:31 So in that form it's inactive, won't bind To the operator. Now

43:36 the active form. 50 fans binding it. And that will be able

43:41 bind to the operator, causing Okay, as in that way.

43:49 . Right. And so um no in that scenario. And then let's

43:59 what's next. So then if the is then utilized and goes away.

44:05 of course it's inactive and you can can transcribe. Okay, so here's

44:11 attenuation mechanism. Okay, So, we're going to transcribe the leader sequence

44:18 . Okay. And there we And so again, the decision has

44:24 be made. Um before we get this orange region here, that's the

44:33 genes. Alright, So there's our kind of structures that can form the

44:41 loops. Okay. 1, Okay, so that's the anti continue

44:48 . 3/4. The attenuated loop. . Um and mm hmm, mm

45:01 . So there's our continually really performing that will ah lead to knocking out

45:09 primaries. Okay, so let's they be going through. Okay. Mm

45:23 . Slow. There we go. . No. Alright, let's get

45:35 as I'm on there. Mm Stop code on. It's the adjacent

45:50 Oden's and those they're in, they're kind of that one region. So

45:55 rivals um stops. It's going to was a stop code and it's going

45:59 overlap on that to region. So here's high defense scenario.

46:10 So there's the river zone begins to , then it's going to do

46:16 So, because again we have lots fans, lots of charged to

46:22 Trh right past these two adjacent trip on stop, stop. And that

46:29 with that two regions. So the informed 34 loop, Tanya loop is

46:35 forms. Okay. And it's right to the people embrace and knocks it

46:45 . Okay, knock it off. we go. And then in the

46:54 defense scenario, mhm. It's going start off the trip code ons.

47:02 . And then that is way far from the plummer is compared to the

47:08 loop and so it's free to keep . Okay? And that's what happens

47:16 on it goes. So um any any questions about that?

47:25 And of course you can you can at yourself and enable the sound and

47:28 the guy narrating you might find that . I just find it annoying.

47:34 that's me. Um Okay, so look at this question to kind of

47:44 that mechanism. Right, so continuation that helps block expression. The trip

47:52 would include all of these except uh see. M. RNA transcript of

47:57 leader sequence. The drivers are installed the crypt cottons of the trip

48:03 Leader sequence information of continuing to high interest several levels of the

48:11 no exceptions. All are required. see. So B. E.

49:27 right. So if we're talking about AIDS saying attenuation mechanism, that's clue

49:33 one sort of blocking expression. So going to occur. Uh when if

49:45 fan is going to be to Okay. Is Hi. Okay.

50:02 And so a of course is going happen whether whatever the scenario you're going

50:07 make the trip leader sequence. so that's that's true. Okay,

50:14 the formation of an attenuated loop. , this is the attenuation mechanism.

50:19 certainly that's what we're going to Okay, I just mentioned depending levels

50:23 high. Right? So that's So I was installed the trip code

50:28 . Okay, so high tryptophan means of charged tr NH which means it

50:34 have to stall, the trip coordinates go through those, install or stop

50:38 the stop code ons or it should okay, so that's the fault.

50:43 , so that's the exception, Writers on the stones at the stop

50:47 of Right? Not there, not . Okay. Um, any questions

50:55 Yeah, so when it's low levels Yes, because they're in charge,

51:08 does that help? Because low, to fan is gonna want to synthesize

51:16 the fan. So by stopping the cardigans, he didn't promote the information

51:21 the anti teenager loop that allows the to keep and transcribing into the structural

51:26 to make trip to fans. So you look at the fan mode,

51:29 almost a matric defense. Yeah, it's immediate. My name doesn't complete

51:44 transcription of Dakota up into the No, there's no trick to fan

51:54 because no trip to fan mean is tR NH for trip to fan.

51:59 basically, when it stops before, it stops at the trip code

52:03 it tells the cell. Uh basically, yeah, but that's what

52:12 lip. Oh because because that, think of that, that leader

52:18 we just take the leader sequence by and plop it in the buffer.

52:22 , it will form that 23 Okay, customers, energetically favorable

52:28 Okay, So um so that the point is you're not forming the

52:35 . Okay, because the 34 is will knock it off. Okay,

52:39 it's more about the 23 loop forms that's the most energetically energetically favorable form

52:44 it's free to form, right? when it stops the stop code

52:47 that is not free to form because being covered up by the Rheiman

52:52 So the 3 4 forms, which the retailer, right? It's real

52:55 to the, to the primaries that it off. Okay, so when

53:00 , when it stalls at the trip ons Then that two region is not

53:05 up. And so the 23 loop , which doesn't really mean anything in

53:09 of interfering with the rivals. And just means that the 34 doesn't

53:13 Okay, because that that is what knock off the preliminaries. The fact

53:18 the forms of 23 loop is really , it forms because it's the most

53:22 favorable luke to form. So just spontaneously. Okay, The loop itself

53:29 the 23 has nothing to do with interfering with the primaries, but that's

53:33 point. It doesn't interfere with It keeps going. What's the connection

53:37 the and the actual Because of the loop forms, it's right in proximity

53:42 that proliferates. That's right there and can mark it off as the 34

53:48 forms, it physically interferes with arrival and knocks it off the transcript so

53:53 it doesn't transcribe. Which is what want when it's in the high tryptophan

54:00 . Right? So it stops at stop but when its stop.

54:08 Right. Because all about positioning on leader sequence and positioning on leader sequence

54:13 what loot performs. So you want look the forms that you want to

54:18 transcription of the trip opera or not that's determined by the levels of tryptophan

54:24 the south. Alright, let's look this table then. Okay, so

54:34 is another way to look at examine it. So low levels of

54:38 versus high levels of trips. So interest rates. Trip levels. Are

54:43 going to synthesize trip to fan? . Um Yes high levels obviously not

54:52 the opteron and low levels of All right. Yes. No.

54:57 a trip co repressor repressor complex form low trip levels. No.

55:05 Over their charter trip. RNA. RNA is plentiful in the low trip

55:13 . No Robertson stalls at gardens in low trip level. Um At the

55:21 code ons and the high trip scenario trip leader sequence forms in the low

55:28 levels. It's the 23 And the one is the attainment of Loot.

55:35 , so just just another way to at it. Okay, so just

55:39 Uh and again as it's, there's gonna be like 50 questions on this

55:44 exam three. Okay. You lick lick, lick opera lack opera

55:50 android different operation in total. Specifically those two things. Maybe four

55:55 Okay, two and two, five the most, but blackly just two

55:59 two. Okay, that doesn't mean understand it because it's only four

56:04 but you know, I'm making a on this only because it takes a

56:10 bit talking to kind of go through see how it works. Okay.

56:15 um but certainly, you know, look at the animations and turn on

56:19 audio, right? That that anything think even text us with it as

56:23 , So but certainly ask me questions you, you know, uh you

56:28 email me. I mean you can about it on monday as well.

56:33 , we just kind of go through animation, listen to it. Um

56:36 think it makes logical sense. so anybody have any questions about it

56:42 be best to kind of like an mull it over right uh and and

56:46 know, there'll be some questions on , you know quiz. So look

56:51 uh get some practice there as Okay, that's all I got for

56:56 , folks. So we'll finish up these other kinds of genes control examples

57:00 monday, And that will finish you three,

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