Paul Allen believes a tipping-point is near in brain research
economist.com
economist.com
First of all, since gene expressions are such upstream information, knowing it won't give us the whole picture (or even come close to it.)
It's like knowing the code of a program, which has syntax you have never seen before, and you have no idea what the compiler does, not to mention the machine code describes an astronomical non-linear computation.
Second of all, gene expression dependents on age, environment, behavior, and probably things we don't even know. I haven't look at the data, but I assume it's just the mouse's brain in one instant. Otherwise it will be a VERY resource intensive job. Not to mention that you have to freeze the brain in order to slice it and map the gene (unless they got better technology now), so even if you get a different instant of the brain it won't be the same mouse.
However, a step towards the goal is a step towards the goal. And that's what this project was. Great work.
Generaly, though, applying high throughput imaging methods to different problems in neuroscience is going to be very fruitful. So in this sense, maybe we're near a tipping point. I don't really think quite yet, though; maybe in a decade or two.
But these are dynamic objects. Google 'rebound excitation' for some counterintuitive effects of inhibitory input. Hard to dissect how circuits of these objects work.
http://icwww.epfl.ch/~gerstner/SPNM/node15.html#SECTION02133...
To help parse figure 2.12:
'Resting potential' = voltage between inside and outside of the neuron in the absence of any excitatory or inhibitory input. It is generated constitutively by ion pumps in the cell.
When cell receives inhibitory input, its voltage drops and it become 'hyperpolarized'. This causes a certain type of calcium ion channel, the 'T-type', to gain the capability of opening (it stops being 'inactivated'). When the inhibitory input ceases, the cell's constitutive ion pumps return it to its resting potential. As the voltage of the cell increases, some T-type channels begin to open, leading to an influx of calcium ions (there are more calcium ions outside the cell than inside), which in turn leads to the cell's voltage to increase further. Now the cell's voltage shoots above its resting potential, and voltage-dependent sodium channels begin to open. Sodium ions rush in, and a spike is generated.
And the payoff to me for trying to a little bit better job of answering your question is that I discovered what looks to be a pretty good resource:
Revolutionary ideas coming from a microsoft cofounder.
(Also, even if he can get into Dorsia, he should stay away from that bimbo Allison Poole, whose liason with Sen. Edwards caused such a fuss...)