Genome Editing with CRISPR-Cas9

Video Statistics and Information

Video
Captions Word Cloud
Reddit Comments

whats their stock?

👍︎︎ 11 👤︎︎ u/redditfetishist 📅︎︎ Aug 11 2016 🗫︎ replies

Is there some video that show the actual procedure to do any of this. Like do you mix things in a flask? Or do you take a Cas and needle it with DNA under a microscope manually? How do they actually do it? What equpment?

👍︎︎ 4 👤︎︎ u/I_AM_shill 📅︎︎ Aug 11 2016 🗫︎ replies

IMO, it's the potential for technologies like this that best explain Fermi's Paradox.

Imagine if nuclear bombs could be made in quantity in your bedroom for a few bucks. We'd be fucked overnight. The only thing protecting us from broken minds is how hard devices of mass destruction are to make.

Perhaps every technological civilization stumbles across the equivalent of the cheap bedroom nuke and disappears shortly thereafter. I've often that it would come from either genetic engineering or nanotechnology. Something like a gene drive (a self-replicating form of CRISPR), which can be done relatively easily by anyone, gives a hint of what that pandora's box might look like.

Maybe it's a race between low barrier of entry mass destruction devices and our understanding of human psychology/neurology so that by the time we have easy means of self destruction, we can fix the impulse some have to use it on our species.

👍︎︎ 4 👤︎︎ u/EricTboneJackson 📅︎︎ Aug 11 2016 🗫︎ replies
👍︎︎ 6 👤︎︎ u/dasjorik 📅︎︎ Aug 11 2016 🗫︎ replies

Welcome, GATTACA

👍︎︎ 4 👤︎︎ u/NearHi 📅︎︎ Aug 11 2016 🗫︎ replies

i understood some of those words

👍︎︎ 2 👤︎︎ u/RPL79 📅︎︎ Aug 11 2016 🗫︎ replies

I read 'gnome' editing. I am not a smart man.

👍︎︎ 1 👤︎︎ u/La_tortuga_grande 📅︎︎ Aug 11 2016 🗫︎ replies

How does a desired sequence get inserted after the cut is made?

👍︎︎ 1 👤︎︎ u/bikemandan 📅︎︎ Aug 12 2016 🗫︎ replies

T-virus

👍︎︎ 1 👤︎︎ u/[deleted] 📅︎︎ Sep 04 2016 🗫︎ replies
Captions
[MUSICAL INTRO] [MUSIC PLAYING] SPEAKER: Every cell in our body contains a copy of our genome, over 20,000 genes, 3 billion letters of DNA. DNA consists of two strands, twisted into a double helix and held together by a simple pairing rule. A pairs with T, and G pairs with C. Our genes shape who we are as individuals and as a species. Genes also have profound effects on health, and thanks to advances in DNA sequencing, researchers have identified thousands of genes that affect our risk of disease. To understand how genes work, researchers need ways to control them. Changing genes in living cells is not easy, but recently a new method has been developed that promises to dramatically improve our ability to edit the DNA of any species, including humans. The CRISPR method is based on a natural system used by bacteria to protect themselves from infection by viruses. When the bacterium detects the presence of virus DNA, it produces two types of short RNA, one of which contains a sequence that matches that of the invading virus. These two RNAs form a complex with a protein called Cas9. Cas9 is a nuclease, a type of enzyme that can cut DNA. When the matching sequence, known as a guide RNA, finds its target within the viral genome, the Cas9 cuts the target DNA, disabling the virus. Over the past few years, researchers studying the system realize that it could be engineered to cut not just viral DNA but any DNA sequence at a precisely chosen location by changing the guide RNA to match the target. And this can be done not just in a test tube, but also within the nucleus of a living cell. Once inside the nucleus, the resulting complex will lock onto a short sequence known as the PAM. The Cas9 will unzip the DNA and match it to its target RNA. If the match is complete, the Cas9 will use two tiny molecular scissors to cut the DNA. When this happens, the cell tries to repair the cut, but the repair process is error prone, leading to mutations that can disable the gene, allowing researchers to understand its function. These mutations are random, but sometimes researchers need to be more precise, for example, by replacing a mutant gene with a healthy copy. This can be done by adding another piece of DNA that carries the desired sequence. Once the CRISPR system has made a cut, this DNA template can pair up with the cut ends, recombining and replacing the original sequence with the new version. All this can be done in cultured cells, including stem cells that can give rise to many different cell types. It can also be done in a fertilized egg, allowing the creation of transgenic animals with targeted mutations. And unlike previous methods, CRISPR can be used to target many genes at once, a big advantage for studying complex human diseases that are caused not by a single mutation, but by many genes acting together. These methods are being improved rapidly and will have many applications in basic research, in drug development, in agriculture, and, perhaps eventually, for treating human patients with genetic disease. [MUSIC PLAYING]
Info
Channel: McGovern Institute
Views: 2,896,355
Rating: 4.9303532 out of 5
Keywords: CRISPR, Cas9, Feng Zhang, Genome Editing, Broad Institute, McGovern Institute for Brain Research at MIT
Id: 2pp17E4E-O8
Channel Id: undefined
Length: 4min 13sec (253 seconds)
Published: Wed Nov 05 2014
Related Videos
Note
Please note that this website is currently a work in progress! Lots of interesting data and statistics to come.