Lifeboat Foundation

Cas13 variants with minimal collateral effect are expected to be more competitive for in vivo RNA editing and future therapeutic applications, researchers claim.

Scientists from the Chinese Academy of Sciences (CAS) have allegedly developed a new “controllable, reversible and safer” gene-editing approach using CRISPR technology.

The system, named Cas13D-N2V8, showed a significant reduction in the number of off-target genes and no detectable collateral damage in cell lines and somatic cells, which indicated its future potential, according to a report published in South China Morning Post newspaper on Wednesday.

Continue reading “Chinese scientists develop new ‘reversible’ gene-editing technique” »

Metamorworks/iStock.

The system, named Cas13D-N2V8, showed a significant reduction in the number of off-target genes and no detectable collateral damage in cell lines and somatic cells, which indicated its future potential, according to a report published in South China Morning Post newspaper on Wednesday.

Researchers have succeeded in making photosynthesis more efficient in soybean plants, in a major breakthrough that will mean less forest has to be cut down to make way for farms.

In the 1980s, biologist Dr Michael Rose started to selectively breed Drosophila fruit flies for increased longevity. Today, the descendants of the original Methuselah flies are held by biotech firm Genescient Corporation and live 4.5 times longer than normal fruit flies.

The flies’ increased lifespan is explained by a significant number of systemic genetic changes — but how many of these variations represent lessons that can be used to design longevity therapies for humans? Dr. Ben Goertzel and his bio-AI colleagues at SingularityNET and Rejuve. AI are betting the answer is quite a few.

SingularityNET and Rejuve. AI have launched a partnership with Genescient to apply advanced machine learning and machine reasoning methods to transfer insights gained from the Methuselah fly genome to the human genome. The goal is to acquire new information regarding gene therapies, drugs or nutraceutical regimens for prolonging healthy human life.

Damage to the ends of your chromosomes can create “zombie cells” that are still alive but can’t function, according to our recently published study in Nature Structural and Molecular Biology.

When cells prepare to divide, their DNA is tightly wound around proteins to form chromosomes that provide structure and support for genetic material. At the ends of these chromosomes are repetitive stretches of DNA called telomeres that form a protective cap to prevent damage to the genetic material.

However, telomeres shorten each time a cell divides. This means that as cells divide more and more as you age, your telomeres become increasingly shorter and more likely to lose their ability to protect your DNA.

Is de-extinction realistic?

Scientists in the US and Australia have announced a multi-million dollar project — resurrecting the extinct Tasmanian tiger. The last known marsupial officially called a thylacine, died in the 1930s. According to the team, the extinct thylacine can be recreated using stem cells and gene-editing technology, and the first one could be “reintroduced” to the wild within 10 years.

We would strongly advocate that first and foremost we need to protect our biodiversity from further extinctions, but unfortunately we are not seeing a slowing down in species loss.

Continue reading “‘Jurassic Park’? Scientists want to resurrect Australia’s Tasmanian tiger” »

Powerful ‘grammar’ allows geneticists to display their data in interactive and scalable illustrations.

Gene therapy pioneer — dr. katherine high, MD — president, therapeutics, askbio.

Dr. Katherine High, MD, is President, Therapeutics, at Asklepios BioPharmaceutical (AskBio — https://www.askbio.com/), where she is also member of the AskBio Board of Directors, and has responsibility for driving the strategic direction and execution of pre-clinical and clinical programs of the company.

Continue reading “Dr. Katherine High, MD — Gene Therapy Pioneer — President, Therapeutics, Asklepios BioPharmaceutical” »

In a new study published in Nature, researchers have developed a breakthrough technique called spatial transcriptomics, which allows scientists to map tumors non-invasively and at an unprecedented resolution depth. For the first time, researchers have created a three-dimensional map of a whole prostate to an unprecedented resolution, including areas of healthy and cancerous cells. Surprisingly, the study revealed that individual prostate tumors contain a range of genetic variations, which until this point were unknown.

“We have never had this level of resolution available before, and this new approach revealed some surprising results,” said Alastair Lamb of Oxford’s Nuffield Department of Surgical Sciences, who jointly led the study.