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Science Llama

@the-science-llama / the-science-llama.tumblr.com

Science, Astronomy, Technology, Art and general Awesomeness
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Last Week In Science

1. The first fully synthetic eukaryotic yeast genome was created

2. We find 50,000 year old DNA in Neanderthal dental plaque and find out what they ate and how they self-medicated

3. New re-usuable sponge can soak up 90x its weight in oil

4. Another first, this time artificial embryos using stem cells

5. Have your mind blown with 3D comparisons of everything in the universe

6. That smell of rain is because of bacteria being launched into the air

7. We found a gene that regulates brain tumor growth

8. Cassini just saw this alien spaceship Ravioli shaped moon named Pan

9. Congress passes a bill telling NASA to beat china send humans to Mars by 2030′s

10. “Fast Radio Bursts” could be aliens traveling across space

11. Scott Pruitt continues to deny that CO2 is main contributor to global warming as he shoves money from fossil fuel companies in to his pocket

12. The brain is 10x more active than we once thought

Their research showed that dendrites are electrically active in animals that are moving around freely, generating nearly 10 times more spikes than somas. The finding challenges the long-held belief that spikes in the soma are the primary way in which perception, learning and memory formation occur.

13. Watch this squid eat a fish twice its size

14. How aborted fetal cells potentially saved billions of lives through vaccines

15. Pigeons with just their veins are freaky (Wellcome Image Awards winners)

16. We test out CRISPR in normal human embryos for the first time and it looks promising

17. Virus-mediated gene therapy treats muscle wasting disease in dogs

18. Treat cancer or disease with gene therapy (In A Box

19. Doing chemistry experiments in the stratosphere because why not

20. A story of Richard Feynman and the 60 year quest to find Gravity Waves

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Swiss biotechnologists have constructed a genetic regulatory circuit from human components that monitors blood-fat levels. In response to excessive levels, it produces a messenger substance that signalizes satiety to the body. Tests on obese mice reveal that this helps them to lose weight.

Humankind has a weight problem – and not only in the industrialised nations, either: the growing prosperity in many Asian or Latin American countries goes hand in hand with a way of life that quite literally has hefty consequences. According to the WHO, over half the population in many industrialised nations is overweight, one in three people extremely so. Not only is high-calorie and fatty food a lifetime on the hips, backside and stomach; it also leaves traces in the blood, where various fats ingested via food circulate. Increased blood-fat values are also regarded as a risk factor for heart attacks and strokes.

Genetic regulatory circuit monitors blood fat

The research group headed by ETH-Zurich professor Martin Fussenegger from the Department of Biosystems Science and Engineering in Basel has now developed an early warning system and treatment: an implantable genetic circuit mainly composed of human gene components. On the one hand, it constantly monitors the circulating fat levels in the blood. On the other hand, it has a feed-back function and forms a messenger substance in response to excessively high blood-fat levels that conveys a sense of satiety to the body.

In order to construct this highly complex regulatory circuit, the biotechnologists skilfully combined different genes that produce particular proteins and reaction steps. They implanted the construct in human cells, which they then inserted into tiny capsules.

The researchers studied obese mice that had been fed fatty food. After the capsules with the gene regulatory circuit had been implanted in the animals and intervened due to the excessive levels, the obese mice stopped eating and their bodyweight dropped noticeably as a result. As the blood-fat levels also returned to normal, the regulatory circuit stopped producing the satiety signal.

"The mice lost weight although we kept giving them as much high-calorie food as they could eat," stresses Fussenegger. The animals ate less because the implant signalised a feeling of satiety to them. Mice that received normal animal feed with a five-per-cent fat content did not lose any weight or reduce their intake of food, says the biotechnologist.

Sensor for different dietary fats

One major advantage of the new synthetic regulatory circuit is the fact that it is not only able to measure one sort of fat, but rather several saturated and unsaturated animal and vegetable fats that are ingested with food at once. How-ever, this development cannot simply be transferred to humans. It will take many years to develop a suitable product. Nonetheless, Fussenegger can certainly envisage that one day obese people with a body mass index of way over thirty could have such a gene network implanted to help them lose weight. Fussenegger sees the development as a possible alternative to surgical interventions such as liposuction or gastric bands. “The advantage of our implant would be that it can be used without such invasive interventions.” Another merit: instead of intervening in the progression of a disease that is difficult to regulate, it has a preventive effect and exploits the natural human satiety mechanism.

This gene network is one of the most complex that Fussenegger and his team have constructed to date and was made possible thanks to the biotechnologist’s years of experience in the field. It is not the first time he and his team have succeeded in constructing such a complex feedback regulatory circuit: a number of years ago, they produced an implant that can also be used to combat gout via a feedback regulatory circuit.

Image 1: Implanted designer cells engineered with a synthetic anti-obesity gene network constantly score the blood fat level of the animals and coordinate excessive blood fat levels to appetite suppression thereby reducing food intake and body weight of diet-induced obese mice on an all-you-can-eat 60 percent fat diet. (Illustration shows diet-induced obese mice of the Jackson Laboratory.) Credit: Graphics: M. Fussenegger / mice photo: Jackson Lab)

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Cats can’t taste sweets.

Yep, also including most meat eaters and all felines from big to small. Because their diet has been mostly meat, the need to taste sweets just wasn’t necessary and the gene required to make part of the sweet receptor protein became ‘broken’. Those spikes, called filiform papillae, are what make cat tongues so rough and help them groom. We have them as well, they are just a lot smaller. Source: Discover / Ed Yong

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It is under popular belief that in order for new genes to come about, there needs to be some kind of random mutation during duplication allowing for that gene to now be able to do something different. If that information is useful, then by natural selection, that gene will prosper and spread. However, the process by which this occurs has been hard to imagine, until now.

Why doesn't that new mutated gene simply get thrown away or repaired and how doesn't that mutation even stick around long enough to form into a newly functioning gene? Well, experiments at Roth's Laboratory among other places, led to a process they call, "innovation, amplification and divergence."

Innovation refers to the gene gaining a second function along side its main function, sort of like when a person picks up a side interest in something. Then, assuming at some point that side specification becomes useful, amplification occurs and the expression of that gene increases. Divergence occurs when the side function becomes so useful that it becomes its own distinct gene. The first function never gets thrown away, in fact nature never throws away good genes it just turns them on or off through epigenetics.

They discovered this by experimenting with Salmonella bacterium, which at first, carried a gene to produce the amino acid histidine with a secondary function to make a different amino acid, tryptophan. That secondary function only assisted the main tryptophan synthesis gene. The main gene for this was removed, forcing the bacterium to learn to re-make tryptophan. It was found that the bacterium was able to make tryptophan again through a duplicated version of the histidine producing gene. This was done through colonizing 3,000 generations on a medium without a tryptophan source.

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