This episode of Real Engineering is brought
to you by Skillshare, home to over 25,000 classes that could teach you a new life skill. On Nov 25th 2018 Dr. He Jiankui announced,
via youtube, that he had decided to push humankind across a controversial threshold. This announcement was, of course, that his
work had resulted in the birth of twins who had both been subject to genetic engineering
using CRISPR. This was a threshold widely considered to
be off limits. In 2015 two of the foremost journals in research,
Science [1] and Nature [2], both made similar statements stating that modification of human
germ cells, that is sperm and egg, should be avoided. The scientific community seemed to have come
to an agreement not to experiment with this technology until we could agree how and when
to apply it to humans, but Dr. He Jiankui has unceremoniously dragged us across this
line in the sand, whether we like it or not. Now, more than ever, there is an urgent need
to stop and ask what the outcomes of this work are for the individuals who have been
subject to it and also how the rest of society may be affected. ... To understand all this we’re going to need
to understand how CRISPR technology works and what the intrinsic shortcomings of this
technology are. DNA is made of nitrogen and carbon based rings
which form 4 distinct chemical codes: Adenine (A), Guanine (G), Cytosine (C) and Thymine
(T). These codes form an easily reproducible double
stranded molecule which is read in group of threes, called codons, which are contained
within structures called genes. These genes are simply the parts of the DNA
that code for the more structurally complex proteins, which in turn, form the biological
machines and structures that are required for all life on earth. Due to DNA’s ability to copy itself, until
now the code in the DNA of all humans can be traced faithfully to the first cells on
earth. Dr. He’s work changed all of this by employing
the use of the CRISPR-CAS9 technology to purposefully change the DNA code in the two twins referred
to as Lula and Nana. As its name suggests, the CRISPR/CAS9 methodology
is dependent on two key parts: CRISPR and CAS9. CRISPR is a kind of repeating DNA structure
that was first discovered accidentally in bacterial DNA by the Japanese scientist Yoshizumi
Ishino in 1987 [3] . For 17 years following this discovery, the exact function of these
DNA repeats went undiscovered until it was identified as the means by which bacteria
identify and protect themselves against invading viral DNA [4]. It turned out that these strange DNA repeats
actually came from viruses. Bacteria have the ability to cut up invading
viral DNA, store it in their own DNA, and then subsequently use it as a guide system
for the enzymes CAS9, which destroys the viral DNA sequence should it invade again in the
future. In order to do this, CAS9 uses the stored
DNA to make something called a guide RNA. This guide RNA is usually coded for by a CRISPR
repeat, and guides CRISPR to DNA it should cut. There are two conditions for CRISPR’s binding
to its target. First Cas9 must bind to the target sequence
and a specific 3 code variation in DNA which is called a PAM (protospacer adjacent motif). Most PAMs can be recognized by Cas9 as they
contain the code: *GG. These recurring patterns are targeted by a
bacteria’s Cas9 system as they identify the DNA of invading viruses. This gives the bacteria an ability to target
and destroy the viral DNA. However, in the last 5 years, we have learned
to leverage this ability to direct CAS9 with guide RNA’s of our own design to alter the
genome of other organisms [5]. The guide RNA binds to a part of CAS9 called
the alpha-helical lobe. In turn, another domain of CAS9, the nuclease
lobe, binds to any flanking part of the DNA strands that matches with the guide RNA, causing
the double helix structure of the DNA to unwind [6]. This process is facilitated by the proximity
between the DNA and the Cas9 complex and electrostatic interactions that occur between the RNA and
DNA. At this point, 2 specific domains of the nuclease
lobe cut the DNA. Although we’re not yet fully sure how this
mechanism occurs, comparative studies suggest that the most likely way is that the two seperate
parts of Cas9 are able to rip protons from water molecules, and in turns weaponize the
deprotonated water molecule to break the DNA apart [ref]. This is done at two sites in the DNA, one
which cleaves the DNA at the target site (HNH) and another which cleaves the DNA at a non-target
site (RuvC). At this point a number of things can happen
depending on which approach is needed: - Cas9 can be modified to include a deaminase
enzyme which can target specific bases for mutation, leading to brand new mutations. - a process known as homology directed repair
can be used to insert new DNA at the cutting site. -Or the targeted piece of DNA can be simply
cut out and removed if it is deemed to be undesirable. Dr. He Jankui opted for the latter option
and simply cut a section out of a gene called CCR5. The section that was cut corresponded to a
mutation known as delta32, that confers it’s owners with protection to certain strands
of HIV. Dr. He’s data seems to suggest he may have
artificially induced a mutation, similar to, but not identical to the delta 32 mutation
in these twins [7]. In order to do this, Dr. He had to first optimize
the gene editing protocol in mice, monkey and human cells. The reason for this is to make sure the protocol
has high specificity - simply put, that the gene editing technique was editing the target
DNA and not some other sequence. This claim is of course key to the validity
of the experiment. Unedited embryos can be thrown away after
all - but for obvious reasons, making unspecific alterations to a human’s genetic code would
be a major red flag...and Dr. He’s work raises major red flags for this exact reason. Their check for specificity of gene editing
used parental genetics as a reference point, an inadequate approach due to the fact that
a parent’s genetic material is subject to a certain degree of randomization every time
a sperm or egg is produced. It’s further complicated by the fact that
no two sperm or eggs will be the same and that their methodology did not account for
the possibility that larger sections of the genetic code could be deleted by their implementation
of the Crispr/Cas9 system. Further to this, from the data released so
far we can tell that the mutation induced in the twins does not exactly mirror the delta32
population that He is attempting to induce in the twins [8]. Although the protein produced should in theory
largely mirror the naturally occuring mutation, we cannot tell that for sure because it has
not been tested. Standard practice at this point is to test
these mutations in an animal model in order to assess unexpected effects of the experiment. This is perhaps the most troublesome part
of this experiment. Lulu and Nana are test subjects for a genetic
mutation that we have not even taken the time and care to test in animals. Nonetheless, the mutation was induced in a
total of 31 human embryos. These embryos were grown for a period of 5-8
days and the 19 that were deemed “normal” were taken forward. Out of these 19 embryos 2 were implanted in
the mother to give rise to the twins. These concerns over Lulu’s and Nana’s
well being are only one of a myriad of issues: Perhaps most critically there was no medical
need for this treatment in the first place. It has been claimed that the biological father
of the twins is HIV positive. Given that the couple used IVF, and that there
is no evidence that HIV would be passed on from father to child using this method of
conception. The procedure was medically unnecessary. Furthermore, He claims to have induced this
mutation completely into at least one of the twins. To do this, He and his group would have had
to check the DNA in every cell in the growing blastocyst, a group of cells that exist from
days 5-9 post fertilization that eventually becomes the embryo. Given that they would have to destroy the
blastocyst to test all the cells, a clear logistical problem exists in trying to qualify
that the mutation exists in all the cells. Accordingly, He and his group only checked
a number of cells from the blastocyst. This means both twins might have a condition
called mosaicism, where the deletion only occurs in a subset of their cells. This means that different cells in their body,
have different DNA. In this context, the effects of this condition
are completely unstudied. Finally, the gene that He took aim at has
also been reported to have a role in learning. A link between the activity of the CCR5 gene
product and the dampening down of the brain’s ability to form new neural connections has
been previously described in mice models. Theoretically, there is a possibility that
the induced deletion could have a positive effect on the twin’s ability to learn. Right now there are far too many unknowns
to make an accurate prediction on what if any effect this experiment will have on the
two twins and there’s an even bigger question about what effect the announcement will have
on the progress of the field. Complicating this mess is the fact that this
study did not go in front of an adequate ethics approval board and default Chinese law prohibits
any kind of follow up with the twins. Because of this, we will likely never know
what will become of Lulu and Nana. Dr. He has stated that he plans to publish
the work in a peer reviewed journal, but given that he has gone M.I.A for almost 2 months
now [9], the scientific community may never have an opportunity to properly review and
digest the impact of this work. So where do we go from here? There is no doubt that genetic engineering
is a valuable tool that can potentially safely increase human wellbeing and productivity. It’s not unlikely that plunging into these
uncharted waters unaccounted and without approval may have a chilling effect on the proper utilization
and development of this technology though. Perhaps, until a consensus on the way forward
is established this is a good thing. Thankfully, the World Health Organization
has stepped up to take a moderating role in the process and are establishing a working
group to establish clear guidelines. We need these guidelines because we’ve stepped
into a new era of medicine. One where the genetic modification of humans
is not only a possibility but an increasingly real option. Humans have long sought to improve themselves
through technology. From the printing press to the internet, these
inventions exist to expand our knowledge and inform us. Maybe one day we’ll be able to alter our
genes to make ourselves smarter, but in the meantime we’re already surrounded by tools
for this, like watching educational videos on YouTube, or watching in-depth tutorials
and classes like the ones you’ll find on Skillshare. Skillshare gives you the perfect place to
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skill to gain. As usual thanks for watching and thank you
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100% this was not about the hiv resistance but about the effect on learning ability.