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Archive for the ‘genetics’ category: Page 500

Feb 29, 2016

Human Babies from CRISPR Pigs

Posted by in categories: bioengineering, biotech/medical, genetics, health

New genetic technologies like CRISPR/Cas9 gene editing and synthetic biology are leading us to entirely new definitions of disease. Now “patients” include people who want children who lack some of their own genes, or have additional ones that they themselves lack. Also among the new patients are people who in the past were too old to have children as well some women who get sick from pregnancy and childbirth, or even the idea of them. Technological advances on the horizon may eventually offer treatment for such conditions.

In February 2015 the British Parliament approved production of “three-parent” children by transferring the nucleus of one woman’s egg into the nucleus-less (“enucleated”) egg of a second woman to avoid the propagation of certain rare “mitochondrial” diseases, Though there were acknowledged risks of the unprecedented procedure (including the possibility of producing novel birth defects), the argument that prevailed was that some mitochondrial diseases are so devastating that it should be tried in the narrowly defined group of prospective mothers carrying defective mitochondria.

Not long afterward, news articles began to appear discussing use of the technique for an entirely different purpose. The procedure’s inventor, the Oregon Health & Science University biologist Dr. Shoukhrat Mitalipov, was now proposing to treat infertility in older women by transferring their egg nuclei into the enucleated eggs of younger women.

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Feb 28, 2016

“Genetic Scissors” Can Completely Eliminate HIV From Cells

Posted by in categories: bioengineering, biotech/medical, evolution, genetics

Thanks to the cocktail of drugs that make up antiretroviral therapy, HIV is no longer a death sentence. But there are downsides to antiretroviral therapy—taking the treatment for many years is expensive, increases drug resistance, and could cause adverse reactions in a patient. And, because the virus stays in reservoirs in the body, the disease can continue to progress in patients if they stop taking their medication.

Now a team of German researchers has found an enzyme that can “cut” the viral DNA out of a cell’s genetic code, which could eradicate the virus from a patient’s body altogether. The proof-of-concept study, published this week in Nature Biotechnology and reported by Ars Technica, was done in mice, but the researchers believe that their conclusions show that this DNA-snipping enzyme could be used in clinical practice. And if it can cut HIV’s genetic code out of a patient’s body, the technique could be a cure for the disease.

The researchers created the DNA-snipping enzyme called Brec1 using directed evolution, an engineering technique that mimics proteins’ natural evolution process. They programmed the enzyme to cut DNA on either side of a sequence characteristic of HIV—a difficult task since the DNA of organisms and of the virus itself mutates often. Still, the researchers identified a well-conserved sequence, then they tested how reliably the enzyme could snip out that sequence in cells taken from HIV-positive patients, in bacteria, and in mice infected with the human form of HIV. After a number of tweaks, Brec1 would cut only that sequence of DNA, patching up the cell’s genetic code once the HIV sequence was cleaved out. After 21 weeks, the cells treated with Brec1 showed no signs of HIV.

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Feb 28, 2016

Gene therapy to save the world

Posted by in categories: bioengineering, biotech/medical, genetics, health, life extension, transhumanism

The most recent Liz talk. According to her in this vid her first test results of telomere length are next month.


Liz Parrish, the Founder and CEO of BioViva Sciences USA Inc, is best known for recently becoming the first person to be treated with gene therapy to reverse aging.

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Feb 26, 2016

Illumina, the Google of Genetic Testing, Has Plans for World Domination

Posted by in categories: biotech/medical, business, genetics, internet

You could say that Illumina is to DNA sequencing is what Google is to Internet search, but that would be underselling the San Diego-based biotech company. Illumina’s machines, the best and cheapest on the market, generate 90 percent of all DNA sequence data today. Illumina is, as they say, crushing it.

But as lucrative as that 90 percent slice is for Illumina now, the whole pie is likely to get even bigger in the future. Less than 0.01 percent of the world’s population has been sequenced so far. So recently, Illumina has made bold moves positioning itself for the future: The company is consolidating its core hardware business—this week, it sued an upstart competitor, Oxford Nanopore Technologies, for patent infringement—while moving into the genetic testing business with new ventures like the liquid cancer biopsy spinoff, Grail.

The company is a looking toward a future in which a lot more people gets genetic tests—and a lot more often. “Grail’s business will be very different than Illumina’s core business,” Eric Endicott, Illumina’s director of global public relations, said in an email. “We are at a tipping point in genomics, where a broad community of scientists and researchers continue to translate the potential of the genome from science to discoveries and applications.”

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Feb 22, 2016

Hybrid Technology Converts Sugar into Nylon

Posted by in categories: engineering, genetics

Now we can turn sugar into Nylon.


Genetically engineered yeast plus electro-catalyst yields bio-based nylon.

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Feb 22, 2016

Breaking Through the Bacteria Barrier

Posted by in categories: bioengineering, biotech/medical, genetics

Breaking the bacteria barriers.


If that field is at just the right magnitude, it will open up pores within the cell membrane, through which DNA can flow. But it can take scientists months or even years to figure out the exact electric field conditions to reversibly unlock a membrane’s pores.

A new microfluidic device developed by MIT engineers may help scientists quickly home in on the electric field “sweet spot” — the range of electric potentials that will harmlessly and temporarily open up membrane pores to let DNA in. In principle, the simple device could be used on any microorganism or cell, significantly speeding up the first step in genetic engineering.

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Feb 21, 2016

Scientists redefine animal classification system; Change confirmed

Posted by in categories: biological, genetics

Scientists have redefined the classification of animals due to genetics; 1st time in 300 years. I wonder how the Vets and the Vet Colleges will respond?


The classification system for animals has been hotly debated and frequently changed since it was created 300 years ago, but now researchers have actually found a genetic basis which confirms that part of the system we use today is actually pretty accurate—and they think this part can be defined even more specifically down to the genetic level.

An international team led by Professor Itai YanaAi of the Technion-Israel Institute of Technology Department of Biology made the discovery after using an extraordinarily powerful technique known as CEL-Seq. CEL-Seq monitors individual cells for their gene activity (as detected via mRNA)—and they applied it across 10 different species, with CEL-Seq being applied to 70 embryos per species.

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Feb 20, 2016

How genetics regulate ageing

Posted by in categories: biotech/medical, genetics, life extension

“Finding that GDF11 levels are under genetic control is of significant interest. Since it is under genetic control, we can find the genes responsible for GDF11 levels and its changes with age,” said the study’s senior author Rob Pazdro, assistant professor at University of Georgia in the US.


Scientists have shown that a hormone instrumental in the ageing process is under genetic control, introducing a new mechanism by which genetics regulate ageing and disease.

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Feb 19, 2016

Scientists say all the world’s data can fit on a DNA hard drive the size of a teaspoon

Posted by in categories: biotech/medical, computing, genetics

Even though it’s looking increasingly likely that humanity will find a way to wipe itself off the face of the Earth, there’s a chance that our creative output may live on. Servers, hard drives, flash drives, and disks will degrade (as will our libraries of paper books, of course), but a group of researchers at the Swiss Federal Institute of Technology have found a way to encode data onto DNA—the very same stuff that all living beings’ genetic information is stored on—that could survive for millennia.

One gram of DNA can potentially hold up to 455 exabytes of data, according to the New Scientist. For reference: There are one billion gigabytes in an exabyte, and 1,000 exabytes in a zettabyte. The cloud computing company EMC estimated that there were 1.8 zettabytes of data in the world in 2011, which means we would need only about 4 grams (about a teaspoon) of DNA to hold everything from Plato through the complete works of Shakespeare to Beyonce’s latest album (not to mention every brunch photo ever posted on Instagram).

There are four types of molecules that make up DNA, which form pairs. To encode information on DNA, scientists program the pairs into 1s and os—the same binary language that encodes digital data. This is not a new concept—scientists at Harvard University encoded a book onto DNA in 2012—but up to now, it had been difficult to retrieve the information stored on the DNA.

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Feb 19, 2016

Biochemical alteration responsible for brain tumor resistance identified

Posted by in categories: biotech/medical, genetics, neuroscience

Glioblastoma multiforme (GBM) is often difficult to treat due to an enzyme (endonuclease DFF40/CAD (Death Fragmentation Factor, 40 kDa subunit / Caspase-Activated DNase)). This enzyme, which is essential for degrading DNA during apoptosis, appears both downregulated and improperly located inside the tumour cells. The researchers observed that overexpression of the enzyme allows the glioblastoma cells to properly degrade their DNA content.


Glioblastoma is the most aggressive manifestation of brain tumours. Due to its high invasive capacity and uncontrolled, infiltrating growth, it is particularly difficult to manage. Currently, the treatment for this disease consists of a combination of surgery (when possible), radiation and chemotherapy. Although current therapy raises the overall survival of patients by around 15 months, it remains inefficient at eradicating tumour cells and, unfortunately, recurrences are another of this cancer’s characteristics.

A team of researchers from the Institute of Neuroscience at the UAB, together with the Hospital Universitari de Bellvitge — ICO, have identified a common molecular alteration in glioblastoma. The researchers observed that the cells of this type of tumour harbour a common intrinsic defect that prevents them from degrading their genetic material during apoptosis, the most important form of programmed cell death induced by radiotherapy and chemotherapy.

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