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I'm standing here in a very beautiful 
spot, as you might see.


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It's not only beautiful, it's also

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a reason to think about what is going 
on with the oceans these days.


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And if I

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look at where I'm standing right now,
I remember that I was collecting


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hydrozoans at a high diversity 30 years ago 
and the one main species I was interested in


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I couldn't find five years ago and
I couldn't find this week so that 


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makes me sad and that should make 
us think about what is going on. 


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Clearly there's a threat to the oceans,
there's global warming, increasing 


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acidification, and a threat to the oceans 
is a threat to the whole planet.


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And what we urgently need is reliable, 
sensitive biomonitoring systems, 


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modern biomarkers, and these modern
 biomarkers require that they can use the


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whole set of genetic tools we have available

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 We need to identify the genes under stress
 immediately when the stress occurs, 


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and interestingly, these genes we're 
interested in for stress response


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related genes we also use for other 
applications, even for biomedical research 


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we can use related gene families to study 
cancer, and actually our <i>Trichoplax </i>


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from here is also used in cancer research.

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Placozoans might be very promising bio

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marker systems for biomonitoring. So 
environmental change related to global 


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warming or ocean acidification

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might be something we could easily 
measure, detect by watching placozoans 


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and their genetics. We have all the tools
 to do that, and I think there's some hope 


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we can develop placozoans into very
 promising biomonitoring systems. 


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What makes a good, promising 
biomarker, biomonitoring system?


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 Well it's genetics. Genetic 
tools are so powerful


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that we can use them now, and we can 
detect changes in the response of an 


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animal system almost immediately.

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So if we know the expression patterns
under normal conditions, we can follow


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the expression patterns under
changing conditions in real time.


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And this is just one way we can use 
genetics in a powerful and good way.


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 We now also have the genetic tools to 
study the setup of polarity in an animal


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bauplan. Polarity is very important, we
 know already that the placozoan bauplan 


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only has polarity, not symmetry,
 just the top-bottom polarity. 


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This polarity is important for the behaviour
for feeding and as we see later also for


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studying cancer genes.

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So we have the tools to study polarity
and polarity is the start for all higher


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animal bodies, so we use polarity also
 to analyse or to study the evolution 


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of higher animal bauplans. So another
 nice thing we can do with genetics is to 


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study the origin or the setup of polarity
and there's all the standard polarity 


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genes we know from higher animals,
 also present in placozoans.


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One of these genes could be trox-2, 
the parahox gene trox-2.


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We have seen what it might be doing in
the videos before when we talked about 


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the evolution of higher animal bauplans from
the placula the so-called placula hypothesis


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and the essential role of this gene is 
also seen if you knock it out so we could


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 do knock-downs of this gene and 
we find as a result that the animals 


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immediately stop dividing. 

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So it's a very essential function and there's
 a lot of work to do with these knock-downs.


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 We've heard a lot of exciting stuff about 
<i>Trichoplax</i>. But now one more exciting stuff 


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is cancer, we mentioned it before. How 
can we use <i>Trichoplax</i> to fight cancer? 


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Well it's very simple: we know <i>Trichoplax</i>

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the only thing it has with respect to 
body plan organisation is polarity. 


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It has a top and a bottom. But we have 
seen it has polarity genes and these 


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polarity genes are the exact genes we
are interested in, because cancer cells


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the first thing cancer cells
 do is they lose polarity.


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If cancer cells lose polarity, they 
grow in all different directions. 


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If they grow in all different directions, it
becomes a clump of cells and we call it


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a tumor. So we need to know what goes on
in the very beginning of losing polarity,


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that we can learn from <i>Trichoplax</i>. 
What we have to do, we take <i>Trichoplax</i> 


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polar <i>Trichoplax</i>, study the polarity 
genes under normal conditions 


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and then we eliminate gravity. If we 
don't have gravity, well then we lose 


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the signal for polarity. 

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We can do it in two ways: we can do it 
here in the lab in a clinostat in a machine 


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which is kind of a simulation of zero 
gravity, or we can do it in reality and


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shoot <i>Trichoplax</i> into space. That's 
what we're going to do in a few weeks. 


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And what do we do with the genetics? 
We just collect the RNA at different stages:


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before losing gravity, after losing gravity
 let's say 10 seconds after losing gravity,


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 a minute, 5 minutes, 10 minutes. So then
we get the first steps of losing polarity.


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 We get the very first genes involved and
 by RNA expression studies, we can find 


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all the genes the medical guys are 
interested in to fight cancer.


