@huttyjuju123 the clamp is simply reffered to as the clamp, the clamp loader haver is also known as the gamma complex which is relayed to the two core enzymes by the tau complex (i.e. linker)
There is a small error. The primer in this video is shown synthesizing RNA primer 3' to 5' which is incorrect because we are on the lagging strand. The primer should work backwards much like how DNA polymerase must work in reverse for the lagging strand. It always goes 5' to 3', and the primase violated this rule in the video.
What if the base pairs of the single loop of the lagging strand match up and link together while the polymerase of the lagging strand is working backwards from the primer? Mutation????
There's another animation showing it slower and more understandable on the link below (just add the three "w" in the beginning), but it has a difference, the RNA primase isn't a part of the protein complex and it correctly adds the primer from 5' to 3'... My biology book clearly says the primase is attached to the helicase which would mean a synthesis from 3' to 5', which one is correct?
please, could anyone write down what the video is saying? It's seems very interesting but unfortunately it's speaks really too fast for a non-english speaker ;(
@MrVexedspirit XD i think we'll get it if we just take some time and reasearch all the components. It's just a little computer. Which is weird. Dna computers work to make a human computer and when that computer achieves intelligence (we can see DNA as being the founding fathers of artificial intelligence XD) we use it to make more computers o.O the Universe is a helluva drug.
@MrVexedspirit I'm guessing you're in highschool - this is university level biology all you need to know is that because DNA is always synthesised in the 5-3 direction , that the lagging strand (5' -3' strand) needs to be synthetised in okazi fragments from RNA primers added by Primase.
this does not explain how the primer on the lagging strand is then removed... by polymerase I, and then how the 'nick' between okasaki fragments is ligased...
Please help here? I am so confused. DNA synthesis is 5' to 3' but the new template made is 3' to 5' right? What about the nucleotides being added? Which direction does that go? The nucleotides are being added to the existing strand in 5' to 3' but after it is added and sealed by ligase, the new strand is antiparallel which is 3' to 5' right? SO, if I have a question which asks the nucleotides are being added in what direction? What is it? 5' to 3' or 3' to 5'???
@Msholyangel17 DNA synthesis is always in the 5' to 3' direction. This is due to the biochemistry of a nucleotide, which has a hydroxyl group (-OH) hanging off carbon 3 of the ribose sugar of the nucleotide, hence 3'. This can only react with a phosphate (part of the triphosphate chain) which is connected to carbon 5 of the nucleotide, hence 5'.
DNA polymerase is uni-directional, it will only ever synthesis in this direction. Are you at graduate level ? also, this video leaves out DNA ligase
@remeader Thank you so much! That does help a lot. So, what about when adding nucleotides? What direction is that? 3' to 5'? I got my BA in biology about 3 years ago. I am preparing for the teachers' certificate exam for Life Sciences 8-12.
@Msholyangel17 It is important that we remember what strand of the DNA we are talking about when discussing DNA replication. For example, the parent strand (the template) could lie with the 3' on the left and the 5' end on the right and we add creating out daughter strand on top, running anti-paralell. If you regard the parent strand, then yes, adding nucleotides are being added 3' to 5', but regarding the newly synthesised strand (daughter strand) it is in the 5' to 3' direction.
missgenie89, You are really confuse. In the figure, upper and rigth, yellow point is 3', and upon and right point is 5', then in blue (lagging) you'll observe adds nucleotides in 3' end. In blue, observe that at right 5' end, and in left 3' end. So, nucleotides adds in 3' end. Correct. Sorry, I don't know read in inglash. So, excuse-me.
Anyone watching this should be aware of recent data that suggest that the factory model is dead, for both prokaryotes and eukaryotes; there is no organization of polymerases as this movie shows.
Is it just me who sees the RNA primase as synthesising the primer from 3' to 5'. I know I get confused with the polarities but it really does look that way. Any confirmation would be appreciated. Thanks
@missgenie89 ,well, I see it too. At first look, I didn't notice, but I guess it is reall wrong. But the mistake isn´t in the primase. If you see it carefuly, this strand is going 3' to 5'. So, the primase is synthesising 5' to 3'. So far so good. But the DNA polimarase is wrong. It is reaaly syntissing 3' to 5´.
My Englis is awfull, but I expect you understand it. :)
@shocs19: On the parental strand, the yellow strain has its 3' end on the right. After the loop, the Pol-III runs along the yellow matrix strand 3' to 5', the complementary nucleotide sequence is therefore elongated 5' to 3', so everything is alright. The primase instead really seems to synthesize the primer 3' to 5', as it runs 5' to 3' on the yellow strand, directly following the replication fork opening.
Unfortunately I'm unable to find more information about this, too.
@missgenie89 The helicase is moving in a 5'-->3' direction along the original lagging whilst the primase must move in a 5'-->3' direction along the new lagging strand. The primosome momentarily revereses its direction to synthesise the RNA primer before continuing in the original helicase dictated direction(Voet,Voet&Pratt Principles of Biochemistry). The main thing this video does is illustrate the trombone model, so the primosome action isnt too crucial. :)
All of the newly synthesized complimentary DNA is elongated/constructed in the 5'-to-3' manner (relative to the strand being made). Whether it's the primer, the leading strand DNA, or the lagging strand DNA, they're all made 5'-3'.
If you're naming it relative to the parent DNA strand, the lagging strand is synthesized on the 3'-5' parent DNA strand, while the leading strand is synthesized on the 5'-3' parent DNA strand.
@missgenie89 The animation is correct. In the leading strand, it goes from 5' to 3' as left to right. In de lagging strand it goes from 5' to 3' as right to left. But the lagging strand in this animation is folded into a loop and to the viewer, it synthesises DNA from left to right.
@missgenie89 Primase does synth RNA primers 3' to 5'. In know in 5' to 3' dNTP incorporation the reaction is driven by the release and hydrolysis of PP but for the RNA primase direction i dont know. I would assume that primase incorporates NTPs not NMPs so the next 5' nuceotide is added with a 3'-OH nucleophilic attack releasing the PP on a NTP already H-bonded on the template. Can anyone help? I'm not sure if this is correct.
@missgenie89 Homochirality is a disaster for naturalistic origins. All amino acids in proteins are 'LEFT-handed', while all sugars in DNA and RNA, and in the metabolic pathways, are 'RIGHT-handed'. Chirality!
A 50/50 mixture of left- and right-handed forms is called a racemate or racemic mixture!!. Which life can't use!! Its what we see in nature and in labs!
Life never came about by time chance natural processes! IMPOSSIBLE!!!
waay o kahverengi olanlar T-Rna dikis makinesi gibi yapmislar :D Ben klavye olarak dusunmustum :P Klavyeden veri girisi gerekli olan protein Ascii kodlari ornegin A=65 8 bit 01-01-10-11 Insulin= 8 bit oldugunu varsay =AT-GS-SG-TA Herbir proteinin ascii kodlari var M-rna (Ram) gecici olarak kopyaliyo, Ribozoma gonderiyo oda Islemci, gelen kodlarda a olusturmak icin gerekli araclari tespit edim T-rna ya gonderiyor ve T-rna tum ihtiyaclari karsilayip getiriyor ve protein olusuyor .Benim yordamim ..
Recent studies show that positive emotion/thought such as love, joy, greatfulness and etc. effects human DNA by making the strands longer and more perceptive (meaning uncoding the hidden talents such as ESP, precognition, clairvoyance and others), when negative emotion such as fear, anger, despair and etc. makes DNA shrink, therefore limiting human perception a great deal. One has to establish an ongoing positive thought in order for these change to occur.
@ABCDOREMI1235 They are Single-Stranded Binding Proteins (SSBs), they are proteins that help keep the two template strands apart from each other while DNA helicase unwinds them.
Yeah I don't think the clamps randomly diffuse to find the RNA template on the lagging strand though. That sounds like a job for the clamp-loading complex of pol3
I think its a bit premature to describe DNA replication as simply as some kind of "type-writer tape-scroll" we simply do NOT know how it works. full stop.
If you learn a little about lipids and bases you will find that it is just a matter of time (lots of time) and the laws of chemistry, and things like this will happen!
People will allmost allways turn to religion when they face something they cannot understand. Time and time again in history we see this, and when it comes to advanced biochemisty, few people actually know how it works.. and as allways, many turn to religion! Dont use sciense to find out what YOU are looking 4, but what it is!
Let me get this straight, these incredibly complex, interactions, with all parts totally reliant on all the other parts functionality and presence, just 'happened'?
By accident?
Yeah, right!
In that case, I have this bridge I wanna sell you.
It's down in Sydney Australia and you can have it for a cool million dollars.
Not by accident, but by beeing super efficient! There is a reason that eukaryotic cells use it still and has not evolved much since they where prokaryotes!
Life is amazing and it follows the laws of chemistry, physics and biology!
@gangsterper Actually, the individual components of a cell cannot be super efficient until they have been formed into a cell. For this to happen, they need to be gathered together, and placed into relationship with one another such that they form an integrated, super efficient whole. That is the part that can't possibly happen by accident.
If you doubt this, check up on enzymes that can survive in water, or chemical reactions that are not degraded by water. When you find some, let me know.
@BigAl53750 Right, but they weren't integrated and exposed to water, there was a phospholipid bilayer, or some sort of precursor to a cell membrane that kept them inside and protected somewhat.
Ah.. sorry! Saw just now that you are a religious retard.. why comment on something you have dont know at all?? I would never start arguing about who did what in that story book we call The Bible!!
The only way this video could be any cooler is if it were playing Raining Blood by Slayer in the background. I like my DNA Replication to be F'ing METAL!
@coneal55 I want to thank you for an epic win because my biology prof showed this video to our class of 100ish students while your comment was visible. Thank you.
The DNA primer is made by DNA primase, but this polymerase only works from 5' - 3', in the video it is synthetised from 3' - 5'. Is the video incorrect?
Nope this video is completely correct. Both strands are being synthesized 5'-3', the method shown here is known as the trombone model. Probably more than what you learned.
Hehe, you should read what I've typed. I'm not talking about synthesising the strands, i'am taling about making the primer for the strand. RNA primase is a 5'-3' proteine, in this video shown, it looks like it is a 3'-5' proteine.
Anyway I asked my prof, and this video should be correct. Since the primer is ~10-15bp long, it can be made on the 5'-3' string without the loop (as you call it trombone)
Looks like a weird sewing machine.
EpicGreenCat 1 day ago
Incomplete info. Good animation, though.
jeydii06 3 days ago
THUMBBBZ UP IF YOUR HERE CAUSE OF AMANDA Y!!11!!!!!
jonk512 5 days ago
her voice makes me uneasy. there's too much... excitement
jessicahomely101 3 weeks ago
I dont understand.. what are these brown balls then..??????
Blackberrypipe 1 month ago
This is not very detailed. .__.
8crazy88 1 month ago 3
lol, wtf am I watching?
soren329 1 month ago
the scary part is i understand all of what she just sped through :|
anfro18 1 month ago
what is the clamp called?
huttyjuju123 1 month ago
@huttyjuju123 the clamp is simply reffered to as the clamp, the clamp loader haver is also known as the gamma complex which is relayed to the two core enzymes by the tau complex (i.e. linker)
SophieDP1 3 weeks ago
@huttyjuju123 B2 subunit of the DNA Polymerase III (Sliding DNA clamp)
jeydii06 3 days ago
WHY YOU SPEAK ENGRISH SO FAST FO??
Qstyles18 1 month ago
2 mins of 'wtf'
456honoka 1 month ago
The music scared me!
heart4evilyn 1 month ago
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If I were an enzyme, I would be DNA helicase so I could unzip your genes
iwashere2011able 1 month ago
Writing it down makes it much easier to learn.
lanalu12 1 month ago
i dont understand whats happening-especially the 2nd half-that was just freaky
Zumerjud 1 month ago
'we' is the last refuge of the man who is afraid to use a more intimate impersonal pronoun
FootDanielLight 2 months ago
I am just so confuse when it starts at
jb12124 2 months ago
Is this the same thing as the holoenzyme in prokaryotes?
kt032 2 months ago
@kt032 no, that is for transcription, not replication
RachelHeather13 1 month ago
There is a small error. The primer in this video is shown synthesizing RNA primer 3' to 5' which is incorrect because we are on the lagging strand. The primer should work backwards much like how DNA polymerase must work in reverse for the lagging strand. It always goes 5' to 3', and the primase violated this rule in the video.
italbello6t9 2 months ago 5
@italbello6t9 You are incredibly right! I watched this video five times at least trying to understand this mistake.
PavelKrupin 2 months ago
That's cute, but what about the remaining primers? Complete the story...
TeodorVonBurg 2 months ago
IM GOING TO KILL MYSFEL :''(
dianafeiteira 2 months ago
@dianafeiteira dont
Shabasky1 2 months ago
its so confusing i still don't get it wt to do!?
losttya 2 months ago
Watched this high and the 2and half of the video rocked my world
randy161616 2 months ago 17
worst fucking video ever...still amazed at the amount of likes!
ProteinFTL 2 months ago
AHHHH where is the clamp loader!!!???
mygrandpappyisafrog 2 months ago
stupid complicated video!!!!
Meltemfb48 2 months ago
brainwashed by second half of the video!!
Romis008 3 months ago
What if the base pairs of the single loop of the lagging strand match up and link together while the polymerase of the lagging strand is working backwards from the primer? Mutation????
miceskin 3 months ago
huh what is going on ???
kajal199560 3 months ago
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i totally understand this.....
MrFunnylicious 3 months ago
Thank you so much for the visualisation! it helps so much when u need to study and understand this process!!!! (n_n) thx!!!!!!
PilotzInTheSky 4 months ago
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mytoiletalk . com
Check out this new funny blog!
numer1pimp1234 4 months ago
There's another animation showing it slower and more understandable on the link below (just add the three "w" in the beginning), but it has a difference, the RNA primase isn't a part of the protein complex and it correctly adds the primer from 5' to 3'... My biology book clearly says the primase is attached to the helicase which would mean a synthesis from 3' to 5', which one is correct?
mcb.harvard.edu/losick/images/trombonefinald.swf
Darkoooooooo 4 months ago
@Darkoooooooo Synthesis is from 5' to 3', as the polymerisation reaction involves addition of a nucleotide to the 3'-OH
MrHypocrism 4 months ago
Comment removed
Darkoooooooo 4 months ago
Oh my God! After hours studying I can finnaly see it. THANKS!
NailAliNaila 4 months ago
thanks for the upload very useful..........
shafran32 4 months ago
Extremely helpful. Wish it would go a little slower though :/
Arenicolous 4 months ago
please, could anyone write down what the video is saying? It's seems very interesting but unfortunately it's speaks really too fast for a non-english speaker ;(
MrsPadlock 4 months ago
creepy music
ntgnr9 5 months ago
I prefer the other animation.
sammy3212321 7 months ago
This is going the wrong way . . . .
pereztr8 7 months ago
Thanks a lot! This clearly shows the lagging strand that is folded back during replication so that the polymerase III dimer can perform a coordinated DNA synthesis on both leading and lagging strands.
jiujiuplus 8 months ago
fuck you! this is fiendishly complicated
MrVexedspirit 8 months ago 49
@MrVexedspirit XD i think we'll get it if we just take some time and reasearch all the components. It's just a little computer. Which is weird. Dna computers work to make a human computer and when that computer achieves intelligence (we can see DNA as being the founding fathers of artificial intelligence XD) we use it to make more computers o.O the Universe is a helluva drug.
Zellig 5 months ago
@MrVexedspirit agreed. there has to be a more basic and straightforward explanation for this horse shit
11cjasp11 3 months ago
@11cjasp11 Oh this IS the simplified explanation son. How complicated it really is would baffle you.
miceskin 3 months ago
@miceskin im no biologist, thats for sure!
11cjasp11 3 months ago
@MrVexedspirit Get to the graduate level, and you will be thankful for this stuff.
TDMagic1 1 month ago
@MrVexedspirit This is for students pursuing bio in College or University. Keep your high school tantrums to yourself.
muzzammil9 1 month ago
@MrVexedspirit I'm guessing you're in highschool - this is university level biology all you need to know is that because DNA is always synthesised in the 5-3 direction , that the lagging strand (5' -3' strand) needs to be synthetised in okazi fragments from RNA primers added by Primase.
SophieDP1 3 weeks ago 2
very helpful. thanks
dukeassa 8 months ago
finalyyyyyyyyyyyyyyyyyyyyyyyyy I unterstoooooood.......thank you soooo much
rockgirl236 8 months ago
this does not explain how the primer on the lagging strand is then removed... by polymerase I, and then how the 'nick' between okasaki fragments is ligased...
jtparker100 9 months ago
For great AS biology videos go to youtube dot com/biologybytes
Biologybytes 9 months ago
I don't like it! There are vids that explain the process much better! It's all about the graphics!
IvanThePeabody 9 months ago
This video has not defined RPA proteins, alothough it shows them. This may confuse viewers who are not familiar with the subject
remeader 9 months ago
Please help here? I am so confused. DNA synthesis is 5' to 3' but the new template made is 3' to 5' right? What about the nucleotides being added? Which direction does that go? The nucleotides are being added to the existing strand in 5' to 3' but after it is added and sealed by ligase, the new strand is antiparallel which is 3' to 5' right? SO, if I have a question which asks the nucleotides are being added in what direction? What is it? 5' to 3' or 3' to 5'???
Msholyangel17 10 months ago
@Msholyangel17 DNA synthesis is always in the 5' to 3' direction. This is due to the biochemistry of a nucleotide, which has a hydroxyl group (-OH) hanging off carbon 3 of the ribose sugar of the nucleotide, hence 3'. This can only react with a phosphate (part of the triphosphate chain) which is connected to carbon 5 of the nucleotide, hence 5'.
DNA polymerase is uni-directional, it will only ever synthesis in this direction. Are you at graduate level ? also, this video leaves out DNA ligase
remeader 9 months ago
@remeader Thank you so much! That does help a lot. So, what about when adding nucleotides? What direction is that? 3' to 5'? I got my BA in biology about 3 years ago. I am preparing for the teachers' certificate exam for Life Sciences 8-12.
Msholyangel17 9 months ago
@Msholyangel17 It is important that we remember what strand of the DNA we are talking about when discussing DNA replication. For example, the parent strand (the template) could lie with the 3' on the left and the 5' end on the right and we add creating out daughter strand on top, running anti-paralell. If you regard the parent strand, then yes, adding nucleotides are being added 3' to 5', but regarding the newly synthesised strand (daughter strand) it is in the 5' to 3' direction.
remeader 9 months ago
@remeader sorry ' we ARE creating out daughter strand' typo !
remeader 9 months ago
i still dont get one thing, why single strand binding proteins stop to attach lagging strand?
fumfulapenguin 10 months ago
This makes it SO much easier to understand!
TheAce0 10 months ago
I feel that it doesn't show the 5'-3' distinction that clearly...but amazing animation nonetheless.
disc33 10 months ago
sweet.
scuzzulus 10 months ago
thanks alot
almushtaq86 11 months ago
lead: 5'---3'
lag: 3'---5'
so if the primer is the compliment of the lagging strand, its direction will be: 5'---3'
deefromott 11 months ago
All the amazing videos are just making me LOVE molecular Bio!!
laure189 11 months ago
Excuse-me, but blue stand (RNA) aren't removed, in lagging stand?
prof3f 11 months ago
@prof3f They are, by DNA Ligase i belive
aamantubillah 11 months ago
missgenie89, You are really confuse. In the figure, upper and rigth, yellow point is 3', and upon and right point is 5', then in blue (lagging) you'll observe adds nucleotides in 3' end. In blue, observe that at right 5' end, and in left 3' end. So, nucleotides adds in 3' end. Correct. Sorry, I don't know read in inglash. So, excuse-me.
prof3f 11 months ago
Don't believe a word of these lies.
Gzorz 11 months ago
Okazaki? Is that from bleach?
devin350z 11 months ago
It's dropping (attaching) the primer 3' to 5', but the replication is occurring 5' to 3'.
Suzeqte 11 months ago
This video explained lagging strand synthesis better in one minute than my professor was able to in 30 minutes. Thanks so much!
RomesFinest 11 months ago
thumbs up if after watching this video you still don't understand DNA replication.
albaskateboarding 11 months ago
Anyone watching this should be aware of recent data that suggest that the factory model is dead, for both prokaryotes and eukaryotes; there is no organization of polymerases as this movie shows.
jegra83 11 months ago
Comment removed
George92ut 1 year ago
are the "orange balls" the Single Strand Binding proteins?
valerioboa 1 year ago
Is it just me who sees the RNA primase as synthesising the primer from 3' to 5'. I know I get confused with the polarities but it really does look that way. Any confirmation would be appreciated. Thanks
missgenie89 1 year ago 16
@missgenie89 ,well, I see it too. At first look, I didn't notice, but I guess it is reall wrong. But the mistake isn´t in the primase. If you see it carefuly, this strand is going 3' to 5'. So, the primase is synthesising 5' to 3'. So far so good. But the DNA polimarase is wrong. It is reaaly syntissing 3' to 5´.
My Englis is awfull, but I expect you understand it. :)
shocs19 1 year ago
@shocs19: On the parental strand, the yellow strain has its 3' end on the right. After the loop, the Pol-III runs along the yellow matrix strand 3' to 5', the complementary nucleotide sequence is therefore elongated 5' to 3', so everything is alright. The primase instead really seems to synthesize the primer 3' to 5', as it runs 5' to 3' on the yellow strand, directly following the replication fork opening.
Unfortunately I'm unable to find more information about this, too.
2BFeXX 1 year ago
@missgenie89 sorry, you're right. XDDD
shocs19 1 year ago
@shocs19 ah sorry, I didn't see your second comment ^^
2BFeXX 1 year ago
Comment removed
George92ut 1 year ago
@missgenie89 The helicase is moving in a 5'-->3' direction along the original lagging whilst the primase must move in a 5'-->3' direction along the new lagging strand. The primosome momentarily revereses its direction to synthesise the RNA primer before continuing in the original helicase dictated direction(Voet,Voet&Pratt Principles of Biochemistry). The main thing this video does is illustrate the trombone model, so the primosome action isnt too crucial. :)
George92ut 1 year ago
Comment removed
adamebiology 11 months ago
Comment removed
nickwho622 11 months ago
@missgenie89
All of the newly synthesized complimentary DNA is elongated/constructed in the 5'-to-3' manner (relative to the strand being made). Whether it's the primer, the leading strand DNA, or the lagging strand DNA, they're all made 5'-3'.
If you're naming it relative to the parent DNA strand, the lagging strand is synthesized on the 3'-5' parent DNA strand, while the leading strand is synthesized on the 5'-3' parent DNA strand.
InternalCorruption 10 months ago
@missgenie89 The animation is correct. In the leading strand, it goes from 5' to 3' as left to right. In de lagging strand it goes from 5' to 3' as right to left. But the lagging strand in this animation is folded into a loop and to the viewer, it synthesises DNA from left to right.
LJZeRRo 10 months ago
@missgenie89 Primase does synth RNA primers 3' to 5'. In know in 5' to 3' dNTP incorporation the reaction is driven by the release and hydrolysis of PP but for the RNA primase direction i dont know. I would assume that primase incorporates NTPs not NMPs so the next 5' nuceotide is added with a 3'-OH nucleophilic attack releasing the PP on a NTP already H-bonded on the template. Can anyone help? I'm not sure if this is correct.
bryantm6 9 months ago
@missgenie89 It is, relative to the template. But if you consider it relative to the RNA strand then it's 5' to 3'.
Fa6ade 7 months ago
@missgenie89 that's exactly my confusion =(
NatalyInsanity 4 months ago
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@missgenie89 Homochirality is a disaster for naturalistic origins. All amino acids in proteins are 'LEFT-handed', while all sugars in DNA and RNA, and in the metabolic pathways, are 'RIGHT-handed'. Chirality!
A 50/50 mixture of left- and right-handed forms is called a racemate or racemic mixture!!. Which life can't use!! Its what we see in nature and in labs!
Life never came about by time chance natural processes! IMPOSSIBLE!!!
5tonyvvvv 2 months ago
waay o kahverengi olanlar T-Rna dikis makinesi gibi yapmislar :D Ben klavye olarak dusunmustum :P Klavyeden veri girisi gerekli olan protein Ascii kodlari ornegin A=65 8 bit 01-01-10-11 Insulin= 8 bit oldugunu varsay =AT-GS-SG-TA Herbir proteinin ascii kodlari var M-rna (Ram) gecici olarak kopyaliyo, Ribozoma gonderiyo oda Islemci, gelen kodlarda a olusturmak icin gerekli araclari tespit edim T-rna ya gonderiyor ve T-rna tum ihtiyaclari karsilayip getiriyor ve protein olusuyor .Benim yordamim ..
omgbbqyax 1 year ago
Not bad, but doean't mention that DNA pol I removes the RNA primers and replaces them with the appropriate DNA sequence.
purplesky001 1 year ago
Comment removed
saracastically 1 year ago
This has been flagged as spam show
Recent studies show that positive emotion/thought such as love, joy, greatfulness and etc. effects human DNA by making the strands longer and more perceptive (meaning uncoding the hidden talents such as ESP, precognition, clairvoyance and others), when negative emotion such as fear, anger, despair and etc. makes DNA shrink, therefore limiting human perception a great deal. One has to establish an ongoing positive thought in order for these change to occur.
RUSSKAYAG 1 year ago
what are the brown circles?
ABCDOREMI1235 1 year ago
@ABCDOREMI1235 They are Single-Stranded Binding Proteins (SSBs), they are proteins that help keep the two template strands apart from each other while DNA helicase unwinds them.
MsWaii 1 year ago
@MsWaii Thank you
ABCDOREMI1235 1 year ago
This didn't make sense to me
iDislikeNames 1 year ago
@iDislikeNames Maybe cause you're a moron.
Zenome 1 year ago
This has been flagged as spam show
@Zenome Go back in your hole, you little troll.
iDislikeNames 1 year ago
This has been flagged as spam show
@Zenome ew go back in your hole you troll
iDislikeNames 1 year ago
@Zenome
That's not very nice.
illmatikkk 1 year ago
excellent!!
juliagoolia181 1 year ago
thank you so much
im fahad from KSA
MrLoool707 1 year ago
its 2d but let me tell you its very undersandable. keep on and make even good videos.
Rshinde951 1 year ago
I guess the little brown "balls" are SSB protein ??
lemongan 1 year ago
annoying voice. sorry.
humanstructureVIDEOS 1 year ago
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this is such a shitty explanation..
xBeowulf 1 year ago
good one
But my tutor taught me that a single DNA polymerase is having two core regions synthesizing the leading and lagging strand
Kukkumolu 1 year ago
@Kukkumolu tutor for biology..hmm
Emil18ftw 1 year ago
@Kukkumolu your tutor is right
Ramouni27 1 year ago
good one
But my tutor taught me that a single DNA polymerase is having two core regions synthesizing the leading and lagging strand
Kukkumolu 1 year ago
good one
But my tutor taught me that a single DNA polymerase is having two core regions synthesizing the leading and lagging strand
Kukkumolu 1 year ago
eee, shoat shet khat nay tar pal >.< @_@ not clear
ceciliawaingei 1 year ago
not a very clear explanation...
Rottentwinkerz 1 year ago
Yeah I don't think the clamps randomly diffuse to find the RNA template on the lagging strand though. That sounds like a job for the clamp-loading complex of pol3
scottietang2 1 year ago
the green balls are called (DNA polymerase III)
and u missed the info about (DNA polymerase I) that replaces the RNA Primers with DNA , and DNA ligase that links the Okazaki Fragments ..
AmroNightWing777 1 year ago
so te baked beans are proteins?
TNeReFFiDeB27 1 year ago
The beta clamps should be on opposite sides...no?
edowney0606 1 year ago
this is my screen saver
soggyrabbits 1 year ago
Thanks! I had a hard time getting my head around the lagging strand but this makes perfect sense.
JennuYasha 1 year ago
her voice is so hypnotic
melodiousby02 1 year ago
Helped me so much in my Biotechnology class!
sikeyourfuckingmind 1 year ago
No mention of ligase....?
Adz795 1 year ago
damn this a good vid... but how should I describe this process with words
DarkFacet 1 year ago
DOES THAT MEAN THAT ALL THE OKAZAKI FRAGMENTS ARE EQUIVALENT??
quirksinlife 1 year ago
scribd (dot) com/nb812
DreamsofMajesty 1 year ago
This video is great. Only I wish you could talk a bit slower so I don't have to pause like a zillion times!
MsMac643 1 year ago
it doesn't mention what happens to the RNA primers, i think they are filled in by DNA ligase?
blazer1211 1 year ago
@blazer1211 Polymerase I replaces the primer with DNA en the Ligase connects the newly placed DNA with the rest of the strand
snikkeltje 1 year ago
@snikkeltje I guess that's the only thing that could be added to this video. Great work anyway!!!
nikolboteva 1 year ago
I think its a bit premature to describe DNA replication as simply as some kind of "type-writer tape-scroll" we simply do NOT know how it works. full stop.
RuniChannel1 1 year ago
My biochemistry professor danced to the music in this video. Made my day.
mrsonsai 1 year ago
very good detail! thanks
jesca215 1 year ago
this video is best video that explane of the DNA replication super easy.
I like this. thank you very much
lightphs 1 year ago 7
any one can tell me what those small round things are?? after the rna primer?? are the dNTPs??
vkarsenal 1 year ago
@vkarsenal Nope they're the single strand binding proteins that keep the 2 DNA chains separated and straightens the chain
oOflanbyOo 1 year ago 3
If i'm not mistaken this depicts the primase syntesizing the RNA primer in the 3'->5' direction. Surely this is wrong?
supermikellillo 1 year ago
If you learn a little about lipids and bases you will find that it is just a matter of time (lots of time) and the laws of chemistry, and things like this will happen!
People will allmost allways turn to religion when they face something they cannot understand. Time and time again in history we see this, and when it comes to advanced biochemisty, few people actually know how it works.. and as allways, many turn to religion! Dont use sciense to find out what YOU are looking 4, but what it is!
gangsterper 1 year ago
Thank you for up loading!!
enjoyu2b 1 year ago
Let me get this straight, these incredibly complex, interactions, with all parts totally reliant on all the other parts functionality and presence, just 'happened'?
By accident?
Yeah, right!
In that case, I have this bridge I wanna sell you.
It's down in Sydney Australia and you can have it for a cool million dollars.
BigAl53750 1 year ago
@BigAl53750
Not by accident, but by beeing super efficient! There is a reason that eukaryotic cells use it still and has not evolved much since they where prokaryotes!
Life is amazing and it follows the laws of chemistry, physics and biology!
gangsterper 1 year ago
@gangsterper Actually, the individual components of a cell cannot be super efficient until they have been formed into a cell. For this to happen, they need to be gathered together, and placed into relationship with one another such that they form an integrated, super efficient whole. That is the part that can't possibly happen by accident.
If you doubt this, check up on enzymes that can survive in water, or chemical reactions that are not degraded by water. When you find some, let me know.
BigAl53750 1 year ago
@BigAl53750 Right, but they weren't integrated and exposed to water, there was a phospholipid bilayer, or some sort of precursor to a cell membrane that kept them inside and protected somewhat.
fbxcore 1 year ago
@BigAl53750
Ah.. sorry! Saw just now that you are a religious retard.. why comment on something you have dont know at all?? I would never start arguing about who did what in that story book we call The Bible!!
gangsterper 1 year ago
AMAZING video!!! thanks so much
kuzminmaya 1 year ago 2
I wonder how much jostling and convection inside ancient thermal vents it took to finally get this thing working right? :)
RammatRamzi 1 year ago
Where does Topoisomerase come into play????
Paakeaswamplands 1 year ago
@Paakeaswamplands : topoisomerase is used to relax the super coling of DNA which i think prior to the unwind of DNA
EriqHover 1 year ago
WOW that is like a little machine. this video is cool
MusicWavesMan 1 year ago 2
DNA = Do Not Abort
Eye2EyeIIIV 1 year ago
The only way this video could be any cooler is if it were playing Raining Blood by Slayer in the background. I like my DNA Replication to be F'ing METAL!
coneal55 1 year ago 78
@coneal55 haha, only on youtube
ironnica 1 year ago
@coneal55 haha, only on youtube
ironnica 1 year ago
This has been flagged as spam show
@coneal55 haha, only on youtube
ironnica 1 year ago
@coneal55
I was going to say Souls of Black by Testament but, yeah I could definately go for some Slayer!
RiffTECK 1 year ago
@coneal55 I want to thank you for an epic win because my biology prof showed this video to our class of 100ish students while your comment was visible. Thank you.
metalheart346 1 year ago
@metalheart346 hahaha my life is now complete
coneal55 1 year ago
@coneal55 Then you dorks would have to argue about:
"Man this is DNA Polymerase Metal mixed with Death metal"
"Naw man this is RNA Primase Metal mixed with funeral chords"
"OMG YA RIGHT THIS IS APPLEBEES METAL"
shoemoodoshaloo 1 year ago
@coneal55 Slayer is awful. Just terrible.
thecareerballoons 1 year ago
@coneal55 there is one thing apart from raing blood, she didnt tell us the proper name for clamp.
dreamrage1 1 year ago
@dreamrage1 there is no name for clamp, its just called DNA clamp
NiagaraSmash 1 year ago
@coneal55 it would be even cooler if the nucleotides coded for the guitar riffs for Raining Blood.
cheddybumpkins 11 months ago
@coneal55 i concur. Slayer rules and Bio rules.
-Bio Club President + Metal Head :-)
bldyi 11 months ago
The DNA primer is made by DNA primase, but this polymerase only works from 5' - 3', in the video it is synthetised from 3' - 5'. Is the video incorrect?
soulsh0t 2 years ago
Nope this video is completely correct. Both strands are being synthesized 5'-3', the method shown here is known as the trombone model. Probably more than what you learned.
wehtam1063 1 year ago
Hehe, you should read what I've typed. I'm not talking about synthesising the strands, i'am taling about making the primer for the strand. RNA primase is a 5'-3' proteine, in this video shown, it looks like it is a 3'-5' proteine.
Anyway I asked my prof, and this video should be correct. Since the primer is ~10-15bp long, it can be made on the 5'-3' string without the loop (as you call it trombone)
soulsh0t 1 year ago
when do you learn about the trombone model?
1aaronaaron1 1 year ago
it looks likes its using some yummy peanuts to feed and produce the new dna =)
pammcake 2 years ago 2
COOLEST VID EVER.
got to love the trippy music and metronome helicase. Watch this when high and know this is happening by the millions inside of you o.O
muzzlesniff 2 years ago