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Journal Samantha Wright's Journal: Biology Help Desk: Volume 3 10

I've received another request for one of these, so I figured that I would put it up. Since they only last about two weeks, please feel free to track me down and ask for a new one if you ever have a question!

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Biology Help Desk: Volume 3

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  • by DaleGlass ( 1068434 ) on Wednesday November 23, 2011 @10:01PM (#38154808) Homepage

    Hi! Thanks a lot for this great opportunity. Hope it's not too much to ask several questions at once.

    I've recently been involved in a discussion on this subject, so several questions came up:

    1. Is genetic engineering on the level of creating catgirls, cabbits [wikipedia.org] and such possible with current technology? I'm guessing that given all the progress and existence of things like glowing fish and GM food, it's probably doable, and the only reason such things don't exist yet is due to ethical and economical reasons. Put in another way, how far could one get into mad scientist territory if ignoring all rules was possible?

    2. Are there limits to gene therapy? If one can artificially create something like the above, is it possible to make an existing organism rebuild itself into the same shape? I understand that it's probably not been attempted, but are there any known limits past which something of the sort wouldn't be worth trying?

    For instance, as somebody with an interest in photography, I think it'd be very neat to be able to improve my vision and become a tetrachromat [wikipedia.org], or gain the ability to see IR or UV. Can gene therapy get something like that done?

    3. What is your opinion on DIYbio [wikipedia.org]?

    Thanks!

    • 1. We don't know nearly enough about morphological and developmental genes to be able to create a complex hybrid of two distant species. In terms of pure needle-and-DNA-replication technology, we have so far been unsuccessful in "booting up" a synthetic cell more complex than the absolute minimal bacterium.

      2. "Rebuilding" is impossible as you describe it, and probably will be for many, many years. Once the body's cells mature into a specific role, they stay put and adopt a certain shape. Reversing that proc

      • by tibit ( 1762298 )

        Isn't the real deal that we don't know how much of genetic information is actually encoded? We have no clue, for example, how to, let's say, change a chosen dimension of our body. So while we can sequence things, and dice-and-splice, we're mostly doing that in the dark, without knowing the exact meaning of a lot of the information? Of course there are certain recipes that simply encode proteins, so if we find a recipe for a protein somewhere in the genetic material, we can change it to make a different one.

        • The human body isn't specified as a 3D model—it's more like a structural induction. We produce components X, Y, and Z at times A, B, and C, and because they have connectors P, Q, and R, electrostatic interactions cause them to spontaneously assemble into a specific final shape. At this point, we know the expression patterns for most of the body's genes (what turns them on and when and for how long), but there's still a large fraction of genes for which we don't know the function. Many of these are pro
          • by tibit ( 1762298 )

            Thank you! That's exactly the insight I was looking for. I gather, then, that real progress in this area will require that we create tools that can work both ways between a 3D model and the inductive representation. So, starting with information in the genome, we extract the inductive representation (the pieces, the connectors, interdependencies, etc), and from that we show how it'll look in 3D. And then, we do changes to the 3D model, and the steps get reversed. At this point it's probably a pipe dream, bu

            • It's definitely a very far ways off—but two centuries might be a little far. I'd say more like sixty years. We'll probably have protein folding cracked in half that time; and, at that point, everyday computers will be advanced enough that running the sufficient scale of molecular dynamics calculations shouldn't be that big a deal. The push toward in silico biology has been an on-going one, since there's no chance of experimental error, and, down the road, we might even be able to avoid the tricky ethi
              • by tibit ( 1762298 )

                It took a 100 years to "crack" something fairly simple in comparison -- computer-based E.E. and mechanical modeling had most of theory done way before then. I claim it'll be no earlier than 200 years from now. We can make a $100 bet, publicly documented here on /., and our great-great-great-grandkids can then settle it. The web never forgets ;) Heck, if I lose the bet, that's all for the better!

  • lead inevitably to DIY biological weapons?

    • Sure—just like DIY explosives. Like any field, regulation will probably be inevitable to prevent such things. That being said, making a biological weapon requires a lot of specialist knowledge, and the pathogens one can engineer in most labs aren't very good at evading the body.
    • As a biochemist myself, I would like to point out that making a biological weapon is not a trivial matter. I think we would likely see DIY chemical weapons before DIY biological weapons. It is pretty easy to make mustard gas or sarin gas into an aerosol and harm people with it. It is actually quite difficult to take something like smallpox and make it into a weapon without hurting yourself.

      From my vantage point I think we'll see biological suicide attackers before we'll see DIY biological weapons. And

Two can Live as Cheaply as One for Half as Long. -- Howard Kandel

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