I was trying to understand the concept of telomeres from such a long time and this video made it crystal clear! Thank you so much!
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊
@Skywalker13693 жыл бұрын
You inverted lagging/leading strands. The leading strand is the one being synthesized continuously (even its RNA primer is replaced by dNTPs). The lagging strand however is synthesized with multiple primers in the form of Okazaki fragments, the final primer being removed on the 5' end, making the lagging strand shorter.
@EasyPeasyLearning3 жыл бұрын
Hi there, leading-strand synthesis generates a blunt end while lagging-strand synthesis produces a long G-rich 3′ overhang, and suggest that variations in lagging-strand synthesis may regulate the rate of telomere shortening in normal diploid human cells. The article supporting this statement is www.ncbi.nlm.nih.gov/pmc/articles/PMC316649/ If you can specify the mistake you detected, we will gladly take a look at that and amend the problem. Thank you
@Skywalker13693 жыл бұрын
@@EasyPeasyLearning Could you explain why? I’m a graduate student in mol bio and I have always been taught that the lagging strand is shorter. Which makes complete sense since its 5’ primer is removed at the end of synthesis. My question to you is why do you think the lagging strand and not the leading strand makes a 3’ overhang?
@EasyPeasyLearning3 жыл бұрын
Hi Raphael, you are mixing 2 different concepts. The 1st concept is that the 3' overhang is on the lagging-strand and the second concept is that after replication the telomere overhang lose a part of DNA due to okazaki fragments. Think it this way if the shorter strand start losing its part of DNA then the quality of life will remain for short time only. Telomere overhang have sequence that is not translating the essential proteins, so losing them little bit is not affecting our quality of life until it reaches the crucial part where it stops dividing anymore. Hope that will clear the confusion.
@Skywalker13693 жыл бұрын
@@EasyPeasyLearning I discussed with my professor who confirmed my points. Many other people also pointed this in the comments. The leading strand is longer. Its overhang is then extended by telomerase to leave more room for polymerase to synthesize the complementary strand
@EasyPeasyLearning3 жыл бұрын
Hi Raphael If you can provide a scientist article or review paper supporting your statement, we will gladly look into it.
@arieelh31703 ай бұрын
omg thank you so much i just started my masters degree and i couldn’t find videos with enough details about this
@EasyPeasyLearning2 ай бұрын
You are welcome 🤗
@esdraswordlyupdates708111 ай бұрын
This is the best video that has answered all inquiries I have been having. Thank you so much.
@EasyPeasyLearning11 ай бұрын
You are welcome 🤗
@KrishnaKumar252613 жыл бұрын
Thank you so much to clear my doubts regarding replication termination
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@johnbates27093 жыл бұрын
Absolutely excellent!
@EasyPeasyLearning3 жыл бұрын
Thank you John 😊
@ronnanwebb41253 жыл бұрын
Now that was perfect . Hope to see these types of explanations for more topics
@EasyPeasyLearning3 жыл бұрын
Thank you 😊
@mohammedal-hammadi50853 жыл бұрын
It's believed that because of the shortening of Telomere, the generations now look shorter than before. Thank you for the great videos
@RockerProf7 ай бұрын
I think some of your concepts are confused. Please refer to a genetics textbook. The leading strand is 3' to 5' and it is synthesized in the 5' to 3' direction. The 5' end of each DNA strand has a primer removed and that leaves the overhang, which is corrected by telomerase, which repairs the overhang.
@مروهجادركريمعبد4 ай бұрын
I think you mean 3’ not 5’ , right¿
@tramymai25012 жыл бұрын
I'm so grateful for your video. I'm struggling with telomere and telomerase until I watch this video. But there is a little mistake in your video - the RNA template, I think it would be Uracil, not Thymine. However, thank you soooooo muchhh
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊 and thanks for the correction 😊 ☺
@rockoquels2 жыл бұрын
Wow! What amazing presentation. Thank you so much.
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊
@dd-ou1bf3 жыл бұрын
Thank you so much...This was a core concept .but you explained it beautifully ...
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@nishathampy17368 ай бұрын
Great video. Nice and neat explanation.
@EasyPeasyLearning8 ай бұрын
Thank you 😊
@motorvehicle13303 жыл бұрын
love this explanation!
@EasyPeasyLearning3 жыл бұрын
Thank you 😊
@minyoongiinfiresme57424 жыл бұрын
Thank you so much for simplifying this topic i now understand it
@EasyPeasyLearning4 жыл бұрын
Thank you 😊
@merttantari7912 Жыл бұрын
Great explanation !! Thank you !!
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@koopck8939 Жыл бұрын
Thank you very much for explaining
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@aysuozbek64784 жыл бұрын
I really like this video, thank you so much. I understand clearly now.
@EasyPeasyLearning4 жыл бұрын
You are welcome 😊
@sidrajabbar72133 жыл бұрын
Thank you !!! You actually made this topic easy peasy💛💛
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@blossomed46953 жыл бұрын
Thak you so much it was so helpful❤
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@janaawada37413 жыл бұрын
THANK YOU!! you made easy peasy
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@oncosaurus57954 жыл бұрын
this video was awesome!!! thank you so much!
@EasyPeasyLearning4 жыл бұрын
Thank you
@noluthandongwenya87592 жыл бұрын
Precise video, thank you!!❤
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊
@declanmoran15712 жыл бұрын
Thanks so much, very well explained
@EasyPeasyLearning2 жыл бұрын
You are welcome 😊
@nighatgull6116 Жыл бұрын
Great explanation ❤
@EasyPeasyLearning Жыл бұрын
Thank you 😊
@rafaela80693 жыл бұрын
Excellent teaching, thanks for this content!
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@yiselmenariveron425 Жыл бұрын
Excellent! Thanks 🙏
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@erzas55610 ай бұрын
This is a good explanation. But the lagging strand should be the one that was actually lagging (Okazaki fragments) which is the black one not the red one. Hope you fix that.
@EasyPeasyLearning10 ай бұрын
Thank you for your comment. I will put correction note on it.
@carlesverdaguer10153 жыл бұрын
Very useful!
@EasyPeasyLearning3 жыл бұрын
Thank you 😊
@saidaquispi9571 Жыл бұрын
Omg me encantó el video ❤❤❤❤ Thank youuuuu
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@FarihaTahsin-f9j3 ай бұрын
Amazing!
@EasyPeasyLearning3 ай бұрын
Thank you 😊
@roxiefox3792 Жыл бұрын
LoL thanks for sharing😊
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@mawadamarei27033 жыл бұрын
Thank you! but I don’t understand.. what about the 5’ tip of the leading strand that appears after removing the primer?! How would the DNA polymerase add to 5’ of the leading strand? Does the same thing of Telomerase happen in this part?
@yintiangiam4782 жыл бұрын
hello i know you asked this question 9 months ago but to answer it, after the primer gets removed, a DNA polymerase with 5’ to 3’ exonuclease activity will replace the primer with DNA versions
@rafiullahkhan9562 Жыл бұрын
@@yintiangiam478only dna polymerase 1 do this 5’--3’ exonuclease avtivity
@enriquemartinezbarton2910 Жыл бұрын
this was so helpful, thank you :)
@EasyPeasyLearning Жыл бұрын
You are welcome 😊
@aryadiyadi10284 ай бұрын
Good explain
@EasyPeasyLearning4 ай бұрын
Thank you 😊
@aryadiyadi10284 ай бұрын
Good media to your take,success for you
@SanmiAdegbusi5 ай бұрын
Impressive
@EasyPeasyLearning5 ай бұрын
Thank you 😊
@muskanseth744010 ай бұрын
Thank you so much 😊😊
@EasyPeasyLearning9 ай бұрын
You are welcome 😁🤗
@ViridianWellness11 ай бұрын
great vıdeo, thank you
@EasyPeasyLearning11 ай бұрын
Glad you liked it!
@augustineraj36624 жыл бұрын
wonderful presentation indeed . congratulations
@EasyPeasyLearning4 жыл бұрын
Thank you
@augustineraj36624 жыл бұрын
Welcome and continue to share your presentations You have very clear concepts
@sheebafarooqui4061 Жыл бұрын
Thanks a lot
@EasyPeasyLearning Жыл бұрын
Most welcome
@panizmoghani2 жыл бұрын
it was perfect. one question is about that kind of people who lives longer than others for example they are more than 100 years old, Does not their telomeres shorten?
@EasyPeasyLearning2 жыл бұрын
Hi Paniz! The time span of telomere shortening varies from person to person. It can depend on different factors like atmosphere, food, weather, physical activity etc etc.
@mounamouna4718 Жыл бұрын
can you please suggest some exercises in molucalar biology !
@arvindrajput53287 ай бұрын
Please elaborate on how cancer cells and telomere
@sarfrazbaber24834 жыл бұрын
Wow liked it
@EasyPeasyLearning4 жыл бұрын
Thanks
@Dunyayibenyoneticem4 жыл бұрын
Thank you but is there something wrong here? I have learned 3’-5’ strand should be lagging and 5’-3’ strand should be leading (parental).
@EasyPeasyLearning4 жыл бұрын
Hi Eda, think it of this way. New strand always get synthesize from 5' to 3' end. Then which strand can make it without problem ? that is 3' to 5' so it is a leading strand. Furthermore look at the textbook again the confusion will get clear. Here i am giving a reference from 1 site. www.quora.com/Why-does-the-lagging-strand-of-DNA-have-to-be-discontinuous Still the confusion remains there. You can contact me again.
@Dunyayibenyoneticem4 жыл бұрын
@@EasyPeasyLearning Yes, new strand always synthesize from 5’ to 3’ . My point is the new 3’-5’ strand that synthesized from 5’-3’ parental strand will synthesize as okazaki fragments so we need a new short RNA for every new Okazaki fragment. When it is time to synthesize tip of new 3’-5’ strand the RNA Primase couldn’t synthesize the tip so we lose telomeric G-tail from parental 5’-3’ strand in every division. We use telomerase to prevent that. So the problem should be in the new and 3’-5’ strand.
@EasyPeasyLearning4 жыл бұрын
Hi Eda, here it needs to be corrected. New okazaki fragments appear on lagging strand is not from 3' to 5'. It is also from 5' to 3' on the parental strand that is also from 5' to 3'. That is why they are in pieces and need primer again and again. This is the detailed article on replication www2.csudh.edu/nsturm/CHEMXL153/DNASynthesis.htm
@AdityaYadav-rw8uv2 жыл бұрын
Superb
@EasyPeasyLearning2 жыл бұрын
Thank you 😊
@doasonmez3684 Жыл бұрын
Its not easy peasy unfortunately 😓 thank you for the video tho 😭
@EasyPeasyLearning Жыл бұрын
I know its really complex but trying my best to make it easy peasy.
@manoranjanbiswal75854 жыл бұрын
Really easy and nice explanation but one doubt not clear as why lagging strand is bigger than leading ...? Not clear
@EasyPeasyLearning4 жыл бұрын
The lagging strand is bigger because it will make up a knot to terminate the process of replication and protect the dna in an intact form (chromosome)
@sanaamen2408 Жыл бұрын
please , do u have video about > Bacterial Transformation: Competence in gram Positive bacteria
@SANAAMYN Жыл бұрын
I need video about transposons
@EasyPeasyLearning Жыл бұрын
Thank you the topic is noted and now is in the queue 😀
@anjinaik81623 жыл бұрын
thank you
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@anujaadbhai32294 ай бұрын
Which book do you refer for this topic?
@psychologieinschema24453 жыл бұрын
are there techniques to shorten telomeres? with proteins? when the DNA is in the histons, are the telomeres outside it? at the end? and can they be attacked then?
@EasyPeasyLearning3 жыл бұрын
Hi Psychologie The advent of the clustered regularly interspaced short palindromic repeats/CRISPR-associated (CRISPR/Cas) system has led to a wide array of targeted genetic studies that are already being employed to modify telomeres and telomerase, as well as the genes that affect them. The article supporting this statement is www.ncbi.nlm.nih.gov/pmc/articles/PMC6406488/ Telomeres normally would not get attacked by nucleases present inside our cell due to the knot made by telomere in the end. Lastly the query about histone attachment with telomere, Specific post-translational modifications of histones, including methylation, acetylation, and ubiquitination, have been shown to be necessary for maintaining a chromatin environment that promotes telomere integrity. The article supporting this statement is www.ncbi.nlm.nih.gov/pmc/articles/PMC6407025/
@psychologieinschema24453 жыл бұрын
@@EasyPeasyLearning thank you very much! i will look at it. is it also possible to mail you? for asking you some more questions?
@psychologieinschema24453 жыл бұрын
@@EasyPeasyLearning hey Easy Peasy, is it possible to ask you something by email?
@EasyPeasyLearning3 жыл бұрын
Hi Psychologie Why don't you ask your questions on our community page. Every subscriber can participate in that and it will be a healthy activity for everyone.
@psychologieinschema24453 жыл бұрын
@@EasyPeasyLearning i understand, but is special question. but is oke
@asannajat61733 жыл бұрын
thank u
@EasyPeasyLearning3 жыл бұрын
You are welcome 😊
@RV_UGGERILAYA7 ай бұрын
How the terp has thymine istead of uracil when u said its a rna strand pls clarify
@EasyPeasyLearning7 ай бұрын
It's a mistake in the video, the correction note is already there
@rafiullahkhan9562 Жыл бұрын
Hey I got one question you said that in telomerase is RNA plus protein so there is uracil instead of thymine but in the video it’s not is it wrong or…?
@EasyPeasyLearning Жыл бұрын
Yes, it was a mistake, we did made a correction note on the video but somehow its not visible all the time.
@lumpyspaceprincess6335 Жыл бұрын
Is aging related to shortining of telomerere or run out of telomeres and become senescent. I mean how could a non-coding DNA prevent aging
@EasyPeasyLearning Жыл бұрын
Hi there, this article might help you in understanding the concept better www.ncbi.nlm.nih.gov/pmc/articles/PMC7152597/#:~:text=Non%2Dcoding%20RNAs%20critically%20regulate,to%20cellular%20senescence%20and%20aging.
@kalpanajha91912 жыл бұрын
shouldn't it be 3'-AAUCCC-5' instead of 3'-AATCCC-5' for the telomerase sequence
@EasyPeasyLearning2 жыл бұрын
Yes you are right it was a mistake in the slide. Thank you for correction
@isnotaddicted3 жыл бұрын
The labeling of the lagging/leading strand is inverted. The leading strand is linearly synthesized by DNA polymerase 5'->3'. Telomerase recognizes the overhang of the leading strand and extends it to repair telomere length, after which RNA primase can add RNA primers to assist DNA polymerase in synthesizing the lagging strand. For structural reasons, both in the case of normal DNA replication and extension of the telomere, RNA primase cannot build the RNA primer at the end of the DNA making the lagging strand shorter. That is part of the reason why the lagging strand is shorter than the leading strand, the other is that nucleases actively shorten then lagging strand to form the t loop structure.
@EasyPeasyLearning3 жыл бұрын
Hi there, leading-strand synthesis generates a blunt end while lagging-strand synthesis produces a long G-rich 3′ overhang, and suggest that variations in lagging-strand synthesis may regulate the rate of telomere shortening in normal diploid human cells. The article supporting this statement is www.ncbi.nlm.nih.gov/pmc/articles/PMC316649/ If you can provide the article claiming that leading strand have overhang, we will gladly want to look upon it and if your statement is true, we will surely amend the video. Thank you
@isnotaddicted3 жыл бұрын
@@EasyPeasyLearning These are two very concepts. Telomere elongation happens just after DNA replication, so strictly speaking the leading and lagging strands do not appear as shown in the video. the newly synthesized leading strand is in complex with its parental strand, and this duplex consists of equal length strands prior to the involvement of telomorase. The newly synthesized lagging strand is similarly in complex with its parental strand, but here the parental strand is longer than the newly synthesized strand (i.e. there is overhang). Instead of labeling the strands in these duplexes as lagging and leading strands, it's better to follow literature convention and name them either 3' and 5' strand or G-strand and C-strand. Alternatively, the strands in the video could be labeled parental strand and newly synthesized lagging strand, as that is the pairing shown. The parental strand is then of course the longer G-rich strand strand ending in 3'. So the concept that the lagging strand has a longer overhang compared to the leading strand is true, but that refers to the duplex of the lagging strand and its template compared to the leading strand and its template. It does not refer to the overhang between two strands in duplex as presented in the video. This confusion likely resulted from mislabeling these strands as leading and lagging, as discussed before. See this image for a schematic view: www.cell.com/fulltext/S0092-8674(09)00897-6
@EasyPeasyLearning3 жыл бұрын
Thank you very much for providing the information. We will definitely look into it and correct everything accordingly. We appreciate your support and feedback.
@tonyx6963 жыл бұрын
Why is the lagging strand longer than leading strand?
@EasyPeasyLearning3 жыл бұрын
Lagging strand is longer to make a knot at the end of a chromosome so that the Dnase enzymes can't degrade it if its open. It is also longer then the leading strand so the telomere depletion would not affect the real Gene's present on the chromosome for a certain period of time.
@tonyx6963 жыл бұрын
@@EasyPeasyLearning but how can the lagging strand be longer if the last okazaki fragment can not be constructed?
@EasyPeasyLearning3 жыл бұрын
Hi Tony, This article will help you understand it. www.nature.com/scitable/topicpage/telomeres-of-human-chromosomes-21041/ www.intechopen.com/chapters/41797
@furkelnurkel3 жыл бұрын
@@EasyPeasyLearning Your source says the leading strand is longer "Thus, as the replication fork moves along the chromosome, one of the two daughter strands is synthesized continuously. The other daughter strand, known as the lagging strand, is synthesized discontinuously in short fragments known as Okazaki fragments, each of which has its own RNA primer. The RNA primers are subsequently degraded, and the gaps between the Okazaki fragments are then filled in by the DNA repair machinery. A problem arises at the end of the chromosome, however, because the DNA repair machinery is unable to repair the gap left by the terminal RNA primer. Consequently, the new DNA molecule is shorter than the parent DNA molecule by at least the length of one RNA primer. Without a solution to this end-replication problem, chromosomes would progressively shorten over many cell divisions, a process that would bring about catastrophic consequences."
@rayanmoosa40692 жыл бұрын
Why we have T in templete in Telomerase it must be U because of RNA template?…
@EasyPeasyLearning2 жыл бұрын
Hi Rayan, yes you are right that was a mistake. Thank you for pointing it out
@NataliaHamukwayah3 ай бұрын
So you mean that the more a person gets old, the more telomerase gets shorter??
@ChemstryBiology Жыл бұрын
why no subtitles
@EasyPeasyLearning Жыл бұрын
Hi there, the subtitles are added to the video, thank you for your comment.