You have NO IDEA how many professors failed to explain this to me and you literally summed it up so well
@user-ms4er6ph8i2 жыл бұрын
Professors xidnt failed to explain u failed to understand bruh
@logicworld2418 Жыл бұрын
😂😂😂😂
@HeyImLucious9 жыл бұрын
For 300k views, I'd expect it to be more indepth. But I guess the title is serious- only focusing on leading v lagging strands. For those who have exams coming and are looking for full info: * DNA synthesis uses semi-conservative replication, meaning the newly synthesized (created) strand is made from a parent strand of DNA (the strand that was separated by DNA helicase). * At the start, DNA topoisomerases and DNA helicases (there are many different types of these enzymes, for simplicity I'll just refer to their group name) bind to the target DNA and begin to "unravel" it. DNA helicase binds to a specific place called the Origin of Replication and unwinds it then separates the strands so other proteins and enzymes can fit in and attach. This separation creates the replication fork/bubble mentioned in the video. * An origin of replication is just a specific sequence of nucleotides that acts as an indicator saying "start replication here!" * After the helicases and topoisomerases have opened up the parent strand of DNA- Primase attaches to the origin and synthesizes complimentary RNA bases. This RNA sequence is called a "primer", it is needed because DNA Polymerases can only add to existing DNA strands. * DNA polymerases (there are many types that do different functions) are enzymes that synthesize complimentary DNA strands. These enzymes are made of many subunits that do specific jobs throughout replication, these subunits activate and deactivate throughout replication when they are needed. (You *shouldn't* need to know the individual subunits of each polymerase for a normal exam, however if you do feel free to reply and I can go into a little more depth ^_^) * DNA replication follows a 5' to 3' direction of replication. The 5' and 3' indicate which carbon we are talking about in the sugar molecule (remember: nucleotides are made of sugar, a phosphate group, and a nitrogenous base). The 5' carbon is attached to the phosphate group The 3' carbon is where the the phosphate group of *another* nucleotide will bond- creating a chain of DNA So, the 5' end will always terminate with a phosphate group and the 3' end will always terminate with a sugar molecule. * This is where the actual video begins. However a few important parts are missing. The lagging strand loops around itself so both the leading and lagging strands are pointing the same direction (5'-3')- this allows simultaneous replication of both strands. Also, while replication is happening, the topoisomerases play another important role. It moves ahead of the replication fork/bubble and breaks the bonds between the parent strands, twists the DNA, and then rebinds the two strands. During replication the DNA strands become more and more strained due to (1) the helicases unwinding and (2) the twisting done by the lagging strand. Topoisomerases relieve the tension and prevents DNA from snapping under the pressure. * The polymerases will also "proof-read" the placed bases to make sure every Adenine is bonded to a Thymine and every Guanine is bonded to a Cytosine. This goes on until replication ends (because either a STOP sequence is reached or the parent DNA strand ends). The cell still needs to deal with the RNA primers at the start of the leading strand and scattered throughout the lagging strand. A polymerase (remember: there are many types of DNA Polymerase enzymes) then removes the primers and replaces them with the correct DNA bases. * After all the RNA is replaced with DNA, ligase comes in and anneals the Okazaki fragments together and the two newly replicated strands bond to form a new copy of DNA. That should be enough info for a quick and exhaustive summary to help with any exams! Also, a few notes. (1) I'm only talking about bDNA. (2) I specifically talk about eukaryotic DNA replication. While eukaryotic and prokaryotic DNA replication are both very similar, they have important distinctions such as: * Prokaryotic DNA is circular and only has one origin of replication * Prok. DNA is larger than Euk. DNA (EDIT: my brain broke for a second here- *Euk. DNA is larger than Prok. DNA.* Sorry!) * There are replication proteins and enzymes unique to both eukaryotic and prokaryotic replication. (3) In order for replication to actually begin, there are specific requirements that must be fulfilled such as all dNTP nucleosides being present and the necessary enzymes/proteins, among other criteria. ~ Source: Pre-med student Good luck! =D
@shifazahid84309 жыл бұрын
thanks alot... can you tell me a little more?? plus i didn't get how prokaryotic dna is larger than eukaryotic?
@shifazahid84309 жыл бұрын
plus i wanna know abt individual enzymes..
@MG-kj2yz9 жыл бұрын
+UnderoathLambofgod Thank you for your explanation it changed my outlook. I don't get too how prokaryotic DNA is larger than DNA Eukaryotic. Because Genom of bacteries are less than Eukaryotic (however Euk. have more DNA molecules and every chromosome will not have whole DNA. I'm still not sure if these DNA molecules are bigger than Euk.). I might be wrong Actually im looking for informations about Telomarase and why it makes DNA shorter I still don't get it so i decided to find answer in diffrent language. I hope that someone will dedicate his time and describe this process :) Sorry if i made a misstake because both English and Bio is not my nattive language :D.
@HeyImLucious9 жыл бұрын
+Shifa Zahid oh wow I completely messed that up at the end! I'm sorry for any confusion, eukaryotic DNA is bigger than Prokaryotic DNA. Besides my (embarrassing) little mistake at the end, which individual enzymes would you like to know about? There are many subunits and helper enzymes! :)
@HeyImLucious9 жыл бұрын
+Marcin Gworys Sorry for the awkward reply times, I'm trying to do this between classes and clinicals. I made a mistake and reversed "Euk" and "Prok" somehow- sorry for the confusion! Eukaryotic DNA is definetly larger than Prokaryotic DNA. Anyways Telomerase is an interesting enzyme. Telomerase itself does *not* make the DNA shorter, ligase makes the telomere shorter after replication. Basically- Telomerase makes a series of repeating 6-bp sequences (known as telomeric sequences) at the ends of chromatids. Why do these exist? Because of the lagging strand made during replication! After exonuclease activity by DNA Polymerase, the Okazaki fragments need to be annealed together to make a complimentary strand. But DNA Polymerases must work in 5' --> 3' directionality, that is they need an -OH group to bind to (see bottom of comment). This is where the telomeric sequences come into play! The end of an Okazaki fragment lacks an -OH group so the DNA Polymerase can't *properly* attach to it. Telomeres provide the -OH group that the Polymerase needs, so a primer comes in and attaches to a part of the telomere ahead of the fragment. Now that the DNA Poly. is attached, it can run down the strand and fill in the gaps between the Okazaki fragments at the end. Then the ligase comes in and attaches all the DNA fragments together. The extra telomeric sequences are then cleaved off so just the completed DNA strand is left and can attach to its complimentary strand. So in summary- Telomerase allows DNA Polymerase to bind and "fix" the lagging strand's Okazaki fragments. Telomeres get shorter because they get cleaved off with the replicated strand that used it. Telomerase (the enzyme that synthesizes telomeric sequences) is very active early in our development, but as we age it gets less and less active. Eventually the telomeres get too short to risk transcription (risk the loss of "important" DNA) so replication stops. Important: Eukaryotic and Prokaryotic cells use different DNA Polymerases (prokaryotes uses DNA Poly III and eukaryotes uses DNA Poly I for this specific exonuclease activity). The DNA polymerase in prokaryotic and eukaroytic cells all serve similar functions. However- they usually have noticeably different structures and extra functions that others do not have. But for simplicity's sake- you're usually safe just thinking of them as a one "polymerase" unless you're in a higher-level course. The -OH group binding is important and explained through biochemistry. I'm not a biochem major, so sadly I can't go into great detail about that because I'm not confident in my answer or reasoning for it (I don't want to give you any false information). Sorry :(
@lilianmuli90386 жыл бұрын
Have been trying to understand these two strands for almost a week now, thank you for making it whole lot easier than I thought... this was very helpful...
@2030games8 жыл бұрын
This helped me a lot! Good luck everybody on your exams reading this! Now stop reading comments and go back to your study!!! :)
@lindelwangema62486 жыл бұрын
You got me
@coretanaroberts736 жыл бұрын
will do!
@sushi_stan5 жыл бұрын
😂😂
@lw93565 жыл бұрын
2030games lol
@hallumilimna86553 жыл бұрын
lol thanks for reminding me to go back and study
@AznSteveLu10 жыл бұрын
I believe it isn't polymerase that fuses the okazaki fragments, but the enzyme ligase.
@darkoshmarko6 жыл бұрын
yes you're correct but DNA polymerase 1 still helps to close the gaps
@SJS0016 жыл бұрын
Yeah
@trafalgarzoro34415 жыл бұрын
It is DNA polymerase that elongates the okazaki fragments though.
@terrickhuang76265 жыл бұрын
@@trafalgarzoro3441 it was called polymerase I before, but scientists change the word to ligase now
@trafalgarzoro34415 жыл бұрын
@@terrickhuang7626 Ohh thanks I was still confused.
@elinessmutakilamfunda14176 ай бұрын
This is the best explanation I've ever come across on this topic
@MichaelHarrisIreland10 жыл бұрын
I'm not stranded anymore. Great video.
@199NickYT10 жыл бұрын
>STRANDed i c wut u did ther
@noorgamer91207 жыл бұрын
Mood
@harshvirkaur53916 жыл бұрын
HA
@biologyexplorer27216 жыл бұрын
Chutiya
@multistan11005 жыл бұрын
@@biologyexplorer2721 language
@amnamirza3377 жыл бұрын
This is the only video that has actually explained clearly the 5' 3' bit! Thankyou so much!!!
@nobeladhikari66028 жыл бұрын
so all i ever needed to know was when you say DNA is built from 5' to 3' you dont mean the original DNA template but the new strand that is being added it !!!!!!
@evilabkxxx34958 жыл бұрын
indeed ,new nucleotides are added to 3'
@googavo1d6 жыл бұрын
DNA polymerase moves from 3 to 5 of DNA template strand
@magicalmuggle5 жыл бұрын
NOBEL ADHIKARI yess 🙌🏼 it becomes much easier when you remember this one point
@andrewhanna51945 жыл бұрын
YES THANK YOU
@agnessteffinia14455 жыл бұрын
Hm have u read the book? All books tell u about the new dna not the original.dna, dont blame her lmao, she was right
@Chitose200710 жыл бұрын
Great video but you forgot to mention the RNA primers required by the okazaki fragments in order for them to be placed upon the strand. The gaps you are referring to do not appear until those primers are removed, they are then refilled with the proper DNA nucleotides.
@tngdrczp1206 жыл бұрын
Arturo Cesar so do the primers on both leading and lagging strand get replaced? By who? Polymerase?
@nikolletadounavi91256 жыл бұрын
By DNA Polymerase that has a exonuclease activity
@federalfreemoneylackofrese993710 жыл бұрын
Good video, but you forgot to talk about primers. Without them DNA Polymerase 3 cannot start replication...
@medupekhumoekae88939 жыл бұрын
I have always wanted an anchor through this whole DNA replication process,never really got a breakthrough until today.Never will I ever struggle again.Thank you very much :)
@rachelmathai22203 жыл бұрын
Great explanation. I could never understand the 5' to 3' process, but you made it digestible. Thank you!
@ankittrivedi29048 жыл бұрын
It was really helpful. I understood the differences between not only leading and lagging strand, but as well as from 5' to 3' confusion. Thank you.
@malihamir94719 жыл бұрын
Thank you so so much! The confusion about why DNA replication takes place in the 5' to 3' direction and the DNA polymerase moves from 3' to 5' direction was really driving me crazy! This video was super helpful! :)
@raghadalmazrouei94853 жыл бұрын
THANK YOUUUUUH from the bottom of my hearttttttttttt. You are just putting all the scientists aside, and having all the attention ❤️. You are not just explaining by reading lines, which many doctors do. Just explained every single point of the concept, and each second and information you have mentioned was necessary. Thank you. My prayers for you.
@minamaher16839 жыл бұрын
Really, thank you .. I have studied this during high school and college, there was no teacher or doctor was able to explain it as simple as you did
@nomanbhutta62809 жыл бұрын
right
@DoctorJammer8 жыл бұрын
As soon as you said "it builds in 5' to 3' direction" instead of it replicates 5' to 3' everything made sense. Differentiating between old strands and the new strands being made was where I was confused. Thank you!
@stewartmichael027 жыл бұрын
Watch at double speed. You're welcome.
@joabmagara21629 жыл бұрын
Very clear and easy to understand. Those complaining, please make a beeline to the nearest library for some voluminous medical pathophysiology text book. Of course details were left out - quite deliberately, and obviously intended in the spirit of "no one left behind."
@Rere-gd8ts9 жыл бұрын
+Joab Magara lol
@POPsongsADDICT10 жыл бұрын
this video is clear and further cements the concept in my head.(my exams are coming soon). however, from what I remember, there are a few missing points (some are asked in the other comments). 1. DNA polymerase requires a free 3' OH end to add nucleotides to. Therefore, an RNA primer, which is a short sequence of ribonucleotides, (synthesized by RNA primase) is needed to provide a free 3'OH end so that the 5' phosphate end in an incoming deoxyribonucleotide can react with the 3' end to form a phosphodiester bond. 2. phosphodiester bond formation is catalyzed by DNA polymerase. 3. the gaps in the lagging strand are actually occupied by RNA primers. 4. When the lagging strand is completed, DNA polymerase replaces the RNA primers with deoxyribonucleotides (close the gaps) 5. after RNA primers are replaced, DNA ligase is the enzyme that catalyses phosphodiester bond formation between the 3' end of a new Okazaki fragment and the 5' end of the growing lagging strand hope I helped
5 ай бұрын
Omg this 12 yr video summed up everything. Throughout the video I was like, "I got it, I got it." Thank you so much and God bless you
@cubetuber40249 жыл бұрын
lol that moment when you're like, "OHHHHHH, I get it now!!!!!"
@idektega42714 жыл бұрын
I read this comment before I watched the video and that’s literally what happened to me😂
@katieonesi64263 жыл бұрын
I had that moment about 3 times throughout the video
@meera-m77343 жыл бұрын
frrrrrrrr
@gulnazboronbaeva53106 жыл бұрын
I've spent couple of hours trying to figure out how DNA synthesis work. Your video made my study easier. Very well explained.
@shariar71519 жыл бұрын
you should do more science videos, because your explanation is very clear and effective
@mashami93254 жыл бұрын
mam,i had a confusion about 5' to 3 ' prime direction.i was trying to know exact mechanism for last 3 hours.finally i viewed your clip.it made me clear.thank u very much.from pakistan
@eddywolfe12308 жыл бұрын
wow this was so much better explained than my professor lol, great video!
@naikmohammad45387 жыл бұрын
yes
@alexlam44553 жыл бұрын
after 8 years, this video is still being used, God bless you, this really clarified stuff up!
@kesshmita22968 жыл бұрын
Thank you so much! I was confused about the whole process but i finally understand how this works. Great video!! :D
@kiyankalati5 жыл бұрын
Oh my goodness, it made so much more sense than possibly any textbook ever written. Thank you so much!
@Malchemist444410 жыл бұрын
Thank you for this great video. Please could you tell me if this statement is true: the template strand is READ in the 3-5 direction, and new DNA is MANUFACTURED in the 5-3 direction.
@samuelbarlow864510 жыл бұрын
true statement
@dazhal827 жыл бұрын
Remember the mnemonic: Read up, write down.
@williamf45245 жыл бұрын
I found this very helpful. You actually explained this better than my professor. For those who say they were expecting more detail, the title of this video is "Leading Strand vs Lagging Strand" . The title tells me that it is just meant to help you identify the leading and lagging strands in a DNA molecule. In my own opinion, I think the detail she went into was just right to explain this concept. If you want even more detail, you may want to look for a video that deals more with the entire replication process as opposed to just identifying leading and lagging strands.
@dkswodud079 жыл бұрын
This cured my cancer
@bonniestanley76909 жыл бұрын
the only video that has stressed the important of the 5' to 3' I now FINALLY fully understand this operation! Thank you!
@SuzyMalekk10 жыл бұрын
You are one hell of tutor! BEST DNA replication video ever!
@jerushaperam63689 жыл бұрын
You're explanation is SO clear. I really needed to understand the Leading and Lagging strand (especially lagging) in order to understand the rest. Everything else, after, is easy bc this has been cleared up! Thanks :)
@emanatelove8 жыл бұрын
I still don't understand how it is added discontinuously. I understand all of the directions. But why are there gaps????
@dimitrismwrakis69108 жыл бұрын
because she didnt tell you anything about the primary fragments in the origins of replication.In the lagging strand primary RNA fragments are built in order to have the elongation.so the leading strand is being built continuously but the lagging strand is being built fragment by fragment between the RNA primars.as you can easily understand there is only one RNA primar in the leading vs many RNA primars in the lagging strand.THUS the one is continuously and the other is not.The video is not the best possible
@aroojtajallah47468 жыл бұрын
well, basically when we talk about the direction of the leading template strand then its 3 prime to 5 prime , and lagging template strand is 5 prime to 3 prime. but new strand is always added from 5 prime to 3 prime direction. so its easy and linear in case of leading strand whose direction is opposit to newly sythesized strand. but in case of lagging strand 5-3 , new strand should be added in 5-3 no matter what, so for lagging strand small okazaki fragments are being introduced ( discountinous strand in 5 to 3 direction).
@bintzubair6 жыл бұрын
Please watch Khan academy videos to clarify that.
@YariXOXOable10 жыл бұрын
thank you soooooo much! the lagging strand being made into Okazaki fragments still confuses me. but you're awesome! glad you took the time to make the video.
@trevster038 жыл бұрын
This was super helpful! My only suggestion would be just to practice the lesson a couple of times before the video to lessen the pauses for filler words! But great job!
@karensellers69368 жыл бұрын
You have no idea how much this just helped me. Thank you so much!!
@natreev52410 жыл бұрын
I appreciate the video. But, you missed a very important concept ( the reason why i watched this video..anyway) Why are there gaps in the lagging strand if it goes from 5' to 3' direction? whats the difference in that 5' to 3' and the 5' to 3' in leading strand? It has to do with looping of the lagging strand. Which, i still do not understand yet. Gonna look it up more. Just wanted to point it out. Thanks for the video again
@ayeshanizam372010 жыл бұрын
I was wondering that way too nouman. I wish i could find more tutorial vids on replication. Do you know of any?Please guide. Thanks
@godetroit9110 жыл бұрын
Okay. I think I finally understand it and can maybe help you. So basically in the Leading strain the DNA polymerase doesn't have to wait for the new information and can follow the RNA Primer, while in the lagging, the Polymerase and the Primer have to dance over each other.
@mahakchauhan411210 жыл бұрын
godetroit91 There are gaps in the lagging strand because everytime the helicase opens the DNA more on the lagging strand, the replication has now to occurs behind the replicated 5-3' segment which is going left to right. a new 5-3 segment which is initiated by the primer starts and later all the primers are replaced by the RNAseH and DNA ligase binds to THEN form one strand like the leading strand. does that make sense? If the process went like leading strand it wouldnt have been a problem but since we go opposite in lagging strand starting from the replication fork(left) down to the 5' end(right) , further opening at the fork by helicase has to be replicated with a new 5-3 end segment.
@zoubidazouzou14817 жыл бұрын
Mahak Chauhan yeaaah thanks to you i understand now how the lagging strand is working 😚
@marianarafik62789 жыл бұрын
I like the fact you mentioned the basic things which are very important as it helped me understand a lot. Thank you so much
@Tragel10210 жыл бұрын
explained it better than my prof
@alannahalloran38592 жыл бұрын
THANK YOU!!!! :-D Ahh I have had such a mental block trying to figure out leading and lagging strands, and just needed a clear, simple explanation like yours. Thank you so much for your help!! Have a great day!
@kundudada90678 жыл бұрын
Why the direction has to be from 5'to 3 '
@hugoherrera77889 жыл бұрын
I had been introduced to this topic today in my AP Biology class and was a little fuzzy about why there was a gap in between the Okazaki Fragments but the explanation given was very helpful, it led to using common sense!
@minhuiseong9307 жыл бұрын
U know, U r genius!!!!n my life saver!! Tremendous thank U!🌞
@keepinitegge93338 жыл бұрын
Thank you so much seriously. I have a huge test today and my teacher just didn't teach us this well. So glad I found this, nice work! Thanks!
@youngchan504411 жыл бұрын
Oh god I wish I got a biology professor like you : ( she just keep flashing ppts and shooting in a hypersonic speed while teaching this
@alexmilevskyy9411 жыл бұрын
Aren't we classmates?! Because my does exactly the same... she must think that we are scientists, and do investigations in our free-time... :/
@mrinmayeeray60499 жыл бұрын
u r an angel .... all my doubts regarding lagging strand got cleared after watching this.
@chrismaher70228 жыл бұрын
I fully understand the evolutionary process, but these complex supporting molecular structures for DNA duplication have evolved as separate entities, having no knowledge of the DNA or the correction processes needed.
@nisgilgit6 жыл бұрын
You did great job explaining and I understood you better than some of the other videos. Keep it up the good work.
@ashleyashleym296910 жыл бұрын
Definitely cleared up a misconception for me but I do feel that it took a little while to get to the point, maybe you should practice what you are going to say prior so it doesn't take as long to deliver what you are saying, but overall great video.
@emilywagner43659 жыл бұрын
This was very helpful to me, the idea is not to understand the entire DNA replication process but to really get a grasp on lagging vs leading (one concept of many in DNA replication). It's a bit choppy but is worth sticking it out if your struggling with this concept. Once she gets going it makes total sense. Thank you!!!!!!!!
@عليقديمي-ر5ك9 жыл бұрын
Thank you so much Really I did not understand this But when I watched this video i got it all Thank you so much again 😍
@danielleboivin88369 жыл бұрын
EXCELLENT Job!!!! Thank you for taking the time to make this video. You are a very intelligent young lady!
@kpshekhawat9 жыл бұрын
very clearly explained
@tylercairo482410 жыл бұрын
You helped a lot with explaining why there are multiple discontinued strands (Okazaki fragments) made! Thank you!
11 жыл бұрын
How the hell did she know I'm having an exam?
@AmritpalSingh-rm8hz6 жыл бұрын
This was so much clearer than the book and its figures. THANK YOU !
@Naytardo9 жыл бұрын
Man i still don't understand this stuff cause i finished at like 4:30 when she was talking about her helix opening up... sorry...
@biologyexplorer27216 жыл бұрын
Sala hutiya
@kittylove1996 жыл бұрын
Thank you so much! This really helped. I have watched so many other videos on DNA replication, but none of them went into enough detail regarding the leading and lagging strand like I needed them too, and they didn't break it down like you did. Thank you for this!! You saved my life
@betterffd10 жыл бұрын
Helpful for straight up basics but not detail. Do yourself a favor and find a different resource.
@briajordan52616 жыл бұрын
My god thank you sooooo so so so much !!!!! These videos have done way more than my textbook, teacher, and notes combined !!!!!! Thank you thank you thanks youuu! It’s the end of the semester and I have to pull 2 A’s out of my butt to pass
@MagentaFerret10 жыл бұрын
HOLY CRAP THIS WAS HELPFUL AS SHIT!!!! THX!!!!!!!!
@chinawyte7 жыл бұрын
I was looking for a video specifically on lagging vs leading since I understand all else....I didn't need "in-depth". Thank you very much!! :)
@afnanali37017 жыл бұрын
زيييين عنااااااااااانييي هو هو
@LEE-sr8uy6 жыл бұрын
your explanation for lagging strand, okazaki fragments is very clear! thank you
@juanfeherreg8 жыл бұрын
helix brakers lol
@KitDKatH10 жыл бұрын
Thank you so much! I was so confused and my test is tomorrow. You're a life-saver!
@godiswithme62713 жыл бұрын
Ur form??
@dehfuzz338 жыл бұрын
ur my waifu
@flydogscanineservices315 жыл бұрын
I thought this was super helpful, I had worked this sort of logic out in my head after getting myself confused. But was glad to find someone else who thinks through it to make sense the same way I did!! It was perfect :)
@miraclensofor652910 жыл бұрын
this video is so clearr and amazing... all my doubts are cleared withing 14mins.... nice!!!!!
@debbiezwi7 жыл бұрын
best explanation I have seen about the lagging mechanism!!! thank you for making this super simple and easy to understand (finally!!)
@aweenkhaffaf62165 жыл бұрын
this was one of the most difficult subject i've been taken in university , and so I've been watch a lot of vedio about DNA replication but they don't make a sense , but hopefully when I watch your vedio it was really good and helpful keep going thank you .
@cookiesarelikecream5 жыл бұрын
aween Khaffaf genetics is even harder ugh
@mihajlostojkovic24655 жыл бұрын
I ve been watching a lot of explanations for DNA replication but I understood when I watched this. You are awesome
@sahrahersi586510 жыл бұрын
YOU ARE A LIFE SAVERRRRRRRRR i wenr from not understanding this at all to being able to teach it to others!! And i have an exam tmrw THANKYOU❤️❤️❤️❤️
@osnapitzvivi10 жыл бұрын
THANK YOU THANK YOU THANK YOU. I was really confused with the Okazaki fragments thing, and now it's way clearer!
@cortexyz9 жыл бұрын
Thanks for this video.....how beautifully you have explained the complex structure in simple words.
@yannimoraites84777 жыл бұрын
Absolutely 100% clear, thanks for making it understandable and the directionality of prime numbers simple to understand.
@nomasikozulu90079 жыл бұрын
Thank you! was getting confused about the leading and lagging strands. you did the basics which made me understand better.
@manasasurya10 жыл бұрын
you saved my life for my test tomorrow! thanks from India!
@maximusmarine8 жыл бұрын
half way through and you're explanations are better than my professor's already
@blazz27924 жыл бұрын
I'm so lost since I have a presentation on this topic but I saw this and watched, and I'm like being rescue from drowning 😂😂 it really help me, thank you soo much, this is my answer.. Omg this is the most compliment I can give..☺ Thanks alot
@TehSwxpe5 жыл бұрын
You taught it better than the head of undergrad research at USF THANK YOU
@timhartmann30918 жыл бұрын
Hey I am German but your Video in English helped me so much more as all the german Vids about DNA Replication. Thank You ;)
@m.p.76518 жыл бұрын
Very helpful video for explaining the leading vs lagging strand. Thank you for sharing this video!
@ZippyandOllie6 жыл бұрын
Thank you so much for the clear video!!! I only really came here for the 5' and 3' confusion, but you answered all my questions hahaha👍🏻😃
@MrRobert468 жыл бұрын
I was having such a hard time understanding the concept of lagging strand and leading strand. My final Exam is in two days!! You just saved my butt! Thank you!!
@taraj2054 жыл бұрын
u explained it so well that i can totally understand what okazaki fragment is!👍🏼
@foz61095 жыл бұрын
Thank u sooo much, this helped me a lot to understand the difference between leading strand and lagging strand. My exam is tomorrow morning and i was really confused until I saw this video, thanks alot keep going ur videos is better even than ma dr teaching ❤️
@Mia-fe7db5 жыл бұрын
Thank you so much for making this video! I felt the same way you did before- I kind of got it, but not completely. But while I was watching your video the light bulb went on and now I really get it! I have a biochemistry test tomorrow and this was very helpful! Thank you so much!
@katelynwaldner91737 жыл бұрын
You saved me! I'm taking grade 12 biology online and DNA replication has been really hard to learn! Thanks so much for this video, the simple terms are appreciated.
@DustinMDEtmanski10 жыл бұрын
DNA Ligase actually joins the Okazaki fragments. Thanks for the video! It really clarifies the process of replication.
@traducoesbr-pt48832 жыл бұрын
Omggg!!! Thank you so much! I was struggling while trying to understand this whole thing ,but you really helped me out thank you smmm!!! Keep on doing these kind of videos!
@zarghamkhatti46253 жыл бұрын
No more questions after watching this video. And this is more confusing me😂 Very nicely teaches. Good work
@jeeva19969 жыл бұрын
Thank you so much this was so helpful, i didn't understand a thing in class but right now i'm a little bit more clear as to what is happening, can't wait to watch more of you videos thanks again :D
@sharleenrivera14875 жыл бұрын
Short, sweet and to the point. PERFECT. THANK YOU!
@lw93565 жыл бұрын
Great to see it from another kid! Simple and easy to understand thank you so much! Got a 90 on my quiz !
@sanelisiweshabalala6537 жыл бұрын
Thank you thank you. Now all that is left for me is to just study in depth but the overview( which I was struggling to grasp) is clear