Science: Animal brought back to life after 30 years

keone

WORLD WAR K aka Sensei ALMONDZ
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Animal brought back to life after spending 30 years frozen
The waterbears were retrieved from frozen moss sample collected in Antarctica in 1983
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Researchers have successfully revived microscopic creatures that had been kept frozen for 30 years.

Tardigrades, also known as waterbears or moss piglets, are tiny water-dwelling organisms. They're segmented, with eight legs, and measure 1mm in length.

Scientists at at Japan's National Institute of Polar Research retrieved the creatures from a frozen moss sample collected in Antarctica in 1983. The sample had been stored at −20 °C for just over three decades.

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Two waterbears were resuscitated. One of them died after 20 days, but the other went on to successfully reproduce with a third specimen hatched from a frozen egg.

It laid 19 eggs, of which 14 hatched successfully.

Found throughout the world, tardigrades can survive extreme pressure, such as deep underwater, and can even live in the vacuum of space for several days.

When they're frozen, the creatures enter a state called cryptobiosis, in which their metabolic processes shut down, and they show no visible signs of life.



"The present study extends the known length of long-term survival in tardigrade species considerably," said researchers.

The previous survival record for adult tardigrades under frozen conditions was eight years, and a much earlier study had suggested that the upper limit for survival under normal atmospheric oxygen conditions was about 10 years.

"We want to unravel the mechanism for long-term survival by looking into damage to tardigrades' DNA and their ability to repair it," said research lead Megumu Tsujimoto.

National Institute of Polar Research now plans to work on examining damage to the water bear's genes and its recovery functions to achieve a better understanding of its long-term survival mechanism.

Hardy though the tardigrades in this study undoubtedly were, they didn't beat the record for survival in a frozen state: that's currently held by a nematode worm that managed nearly 39 years.
 
This is why it's impossible for all life on earth to ever be extinguished. The microcosmic world is truly amazing.

It's nowhere near as ugly looking like it is in that first rendering as it is in the actual video.
 
I am stepping outside my lane of knowledge but I can see future generations of scientist splicing tartigrades genomes with humans to take advantage of their robust ability to survive in extreme conditions -

If we had a time machine into the future - our progeny will not look like us at all - we will be like Neanderthals to them.
 
I am stepping outside my lane of knowledge but I can see future generations of scientist splicing tartigrades genomes with humans to take advantage of their robust ability to survive in extreme conditions -

If we had a time machine into the future - our progeny will not look like us at all - we will be like Neanderthals to them.

That's pretty fascinating and nearly impossible at this stage of bio-engineering! One of the cool things with SyFy is you can create these monsters of the week spliced out of genomic material from species A and species B to confer some amazing abilities.

In reality as you can imagine that shit is complicated and involved as hell! One of the projects I was involved in during undergrad was essential based on the exactly what you're purposing here! Especially taking the properties of one "species" and conferring it onto another.

Here are some of the biggest hurdles:

1) The two species have to be a phylogeny(Essentially Family)
2) Identify the genes for a particular trait especially for something as "involved" for what the waterbear can do is incredible difficult. Even if you've coded for it's entire genome! Something that we don't have the bio-tech to do at this time. Not to mention there is still quite a lot we don't understand.
3) Let's say somehow you managed to isolate all the particulars of said trait. How to introduce it and MOST IMPORTANLY getting it to take in a cluster of selective "progeny" is ridiculously notorious! Species aren't design as they currently are to take on a brand new "transgene" without a hella of a fight!

Fascinating stuff really!
 
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That's pretty fascinating and nearly impossible at this stage of bio-engineering! One of the cool things with SyFy is you can create these monsters of the week spliced out of genomic material from species A and species B to confer some amazing abilities.

In reality as you can imagine that shit is complicated and involved as hell! One of the projects I was involved in during undergrad was essential based on the exactly what you're purposing here! Especially taking the properties of one "species" and conferring it onto another.

Here are some of the biggest hurdles:

1) The two species have to be a phylogeny(Essentially Family)
2) Identify the genes for a particular trait especially for something as "involved" for what the waterbear can do is incredible difficult. Even if you've coded for it's entire genome! Something that we don't have the bio-tech to do at this time. Not to mention there is still quite a lot we don't understand.
3) Let's say somehow you managed to isolate all the particulars of said trait. How to introduce it and MOST IMPORTANLY getting it to take in a cluster of selective "progeny" is ridiculously notorious! Species aren't design as they currently are to take on a brand new "transgene" without a hella of a fight!

Fascinating stuff really!
Man I met a guy who did some genome mapping research of his on and his sequencer machine cost him, I believe he said 750g's and for one line of code they had to sift through a phone book of junk information... And this was for a particular code with a particular marker sequence, now imagine trying to do that shit for some unknown gene that we have no idea how it looks like...
Not being an expert on the subject, but to me that seems damn near impossible...
 
Man I met a guy who did some genome mapping research of his on and his sequencer machine cost him, I believe he said 750g's and for one line of code they had to sift through a phone book of junk information... And this was for a particular code with a particular marker sequence, now imagine trying to do that shit for some unknown gene that we have no idea how it looks like...
Not being an expert on the subject, but to me that seems damn near impossible...


Man this coding shit is serious
 
Man this coding shit is serious
Many people who are working on it, including the guy I talked with, are fucken savant who has the brain to sit down and do just one thing in life... I really believe that Jewish people (in particular the Ashkenazi Jews) intentionally breed in a way to produce these types of individuals and this is the reason why they have such a high amount of autism..
Matter of fact the same genome guy, practically admitted the shit, before the Director of the symposium I was attending whisked off the stage before allowing him to spilling the beans...
This is why I sought to talk to him privately, and in the middle of our convo, the same Rabbi Director who got him off the podium was there with me trying to pick his brains for more information.
He was obviously the brightest guy in the building and yet he felt his knowledge should not be shared with the others, yet he wanted it for himself... Hmmmmmmm...
 
Man I met a guy who did some genome mapping research of his on and his sequencer machine cost him, I believe he said 750g's and for one line of code they had to sift through a phone book of junk information... And this was for a particular code with a particular marker sequence, now imagine trying to do that shit for some unknown gene that we have no idea how it looks like...
Not being an expert on the subject, but to me that seems damn near impossible...

Yep! There are a couple of things to sequencing. When you're working on a project and you need sequencing work done you usually start by "tagging it" the region of code/gene of interest that you want sequenced. Typically this is outsourced to a company with powerful machines that do this and as you can imagine it's expensive as hell and most charge per line of code. Also, since likely you don't know exactly what your looking for then you going to ask for the entire genome! Remember how long it took J Craig Venter and his team to sequence a human via "The human genome" project? Realize there are some species of plants with more genomic material than people.

Now, Let's say you sequenced the entire genome for this Tardi species...now what? You have volumes and volumes of genetic code. Trying to figure out what a specific line of code does is astronomical! BTW, We still haven't figured out a good portion of what all our genomic material is all about and this is with Billions of dollars and resources invested by pharmaceuticals companies and others studying certain things..Cancer being at the top of the list

1) A line of code for a gene "rarely" operates on it's own and is normally associated with a cascade of other process associated with who the hell knows what!
2) Typically to figure out #1 means you're going to have to freeze,homogenized, purify and eventually sequence this creature at every instant towards whatever it is your trying to study. In combination with some sorta Real-Time(RT) ASSAY whose purpose is to map typically Enzyme-Substrate interactions coded from proteins derivates of translated genes. Once more triggered by who knows what single or cascade of things.

#1 and #2 is just to build what the industry calls a Library!

Lets further supposed years+ later you figure out exactly what does what! That's just part of your solution. Now trying to splice that trait into a species that doesn't exhibit said trait naturally is a can of worm in itself. Between nothing happening, rejection and deleterious mutations being the likely results it working as it did in your host species is highly improbable!
 
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This was on the science channel last year. They can freeze and thaw out on their own. They can also live in space.
 
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