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Category: genetics – Page 202

An AAV-CRISPR/Cas9 strategy for gene editing across divergent rodent species

Crispre cas 9.

A major issue in neuroscience is the poor translatability of research results from preclinical studies in animals to clinical outcomes. Comparative neuroscience can overcome this barrier by studying multiple species to differentiate between species-specific and general mechanisms of neural circuit functioning. Targeted manipulation of neural circuits often depends on genetic dissection, and use of this technique has been restricted to only a few model species, limiting its application in comparative research. However, ongoing advances in genomics make genetic dissection attainable in a growing number of species. To demonstrate the potential of comparative gene editing approaches, we developed a viral-mediated CRISPR/Cas9 strategy that is predicted to target the oxytocin receptor (Oxtr) gene in 80 rodent species. This strategy specifically reduced OXTR levels in all evaluated species (n = 6) without causing gross neuronal toxicity. Thus, we show that CRISPR/Cas9-based tools can function in multiple species simultaneously. Thereby, we hope to encourage comparative gene editing and improve the translatability of neuroscientific research.

The development of comparative gene editing strategies improves the translatability of animal research.

Do We Share DNA with ET?

Year 2020 o.o!!!

The primary difficulty of interstellar communication is finding common ground between ourselves and other intelligent entities about which we can know nothing with absolute certainty. This common ground would be the basis for a universal language that could be understood by any intelligence, whether in the Milky Way, Andromeda, or beyond the cosmic horizon. To the best of our knowledge, the laws of physics are the same throughout the universe, which suggests that the facts of science may serve as a basis for mutual understanding between humans and an extraterrestrial intelligence.

One key set of scientific facts presents an intriguing question. If aliens were to visit Earth and learn about its inhabitants, would they be surprised that such a wide variety of species all share a common genetic code? Or would this be all too familiar? There is probable cause to assume that the structure of genetic material is the same throughout the universe and that, while this is liable to give rise to life forms not found on Earth, the variety of species is fundamentally limited by the constraints built into the genetic mechanism.

On Earth we have only sequenced the genomes of a small percentage of living organisms and have only recently completed the human genome. We have successfully cloned several animals, but technical and ethical roadblocks prevent scientists from doing the same with humans. If an extraterrestrial civilization isn’t burdened with ethical dilemmas about cloning, however, sending the genetic code for humans and other species may be the most effective way to teach them about our biology.

Fish evolution takes place in decades — not millions of years

Given this new information humans could modify their genetic code to rapidly accelerate their evolution aswell leading to a biological singularity of evolution.

Codfish have been telling a story of rapid fish evolution, reshaped by human activity more swiftly than previously assumed, reveals a cutting-edge study led by Rutgers University.

This evolutionary tale, illuminated during the latter half of the twentieth century, signifies the impact of human-driven overfishing. The findings suggest that evolutionary changes, once thought to span millions of years, can be catalyzed within mere decades.

The report, sharing the first genomic evidence of such accelerated evolution in Atlantic cod, has recently been published in the journal Philosophical Transactions of the Royal Society B: Biological Sciences.

The Primate Genome Project unlocks hidden secrets of primate evolution

Researchers from Zhejiang University, Kunming Institute of Zoology, Northwest University, and Yunnan University, Aarhus University, and BGI-Research have jointly led a series of significant new studies are published in a special issue of the journal Science, and in papers in Nature Ecology & Evolution and Science Advances.

Co-led by Guojie Zhang from Centre for Evolutionary & Organismal Biology at Zhejiang University, Dong-Dong Wu at Kunming Institute of Zoology, Xiao-Guang Qi at Northwest University, Li Yu at Yunnan University, Mikkel Heide Schierup at Aarhus University, and Yang Zhou at BGI-Research, the Primate Genome Consortium reported a series of publications from its first phase program. The program includes high quality reference genomes from 50 , of which 27 were sequenced for the first time. These studies provide new insights on the speciation process, , social , sex chromosomes, and the evolution of the brain and other biological traits.

The comparative analysis of primate genomes within a phylogenetic context is crucial for understanding the evolution of the human genetic architecture and the inter-species genomic differences associated with primate diversification. Previous studies of primate genomes have focused mainly on primate species closely related to humans and were constrained by the lack of broader phylogenetic coverage.

Researchers link death in gene-editing study to a virus used to deliver the treatment, not CRISPR

The lone volunteer in a gene-editing study targeting a rare form of Duchenne muscular dystrophy likely died after having a reaction to the virus that delivered the therapy in his body, researchers concluded in an early study.

Terry Horgan, 27, of Montour Falls, New York, died last year during one of the first tests of a gene-editing treatment designed for one person. Some scientists wondered if the gene-editing tool CRISPR played a part in his death. The tool has transformed genetic research, sparked the development of dozens of experimental drugs, and won its inventors the Nobel Prize in 2020.

But researchers said the virus — one used to carry treatment into the body because it doesn’t usually make people sick — combined with his condition, triggered the problems that ultimately killed him.

This Woman Feels No Pain. Decoding Her DNA Could Bring Relief to Millions

Jo Cameron is a 75-year-old Scottish woman who has gone through life without experiencing significant pain of any kind. Even major surgery and childbirth failed to deliver the discomfort most of us would experience.

According to an interview with the BBC in 2019, Cameron only knows her skin is burning if she smells or sees it. To her, suffering is nothing more than an abstract concept.

The quirk that Cameron was born with is shared with just a few other people in th e world. Called congenital analgesia, it is a one-in-a-million condition with multiple genetic causes that may come with other symptoms, such as sweating more or having no sense of smell.

Geneticists discover hidden ‘whole genome duplication’ that may explain why some species survived mass extinctions

Geneticists have unearthed a major event in the ancient history of sturgeons and paddlefish that has significant implications for the way we understand evolution. They have pinpointed a previously hidden “whole genome duplication” (WGD) in the common ancestor of these species, which seemingly opened the door to genetic variations that may have conferred an advantage around the time of a major mass extinction some 200 million years ago.

The big-picture finding suggests that there may be many more overlooked, shared WGDs in other species before periods of extreme environmental upheaval throughout Earth’s tumultuous history.

The research, led by Professor Aoife McLysaght and Dr. Anthony Redmond from Trinity College Dublin’s School of Genetics and Microbiology, has just been published in Nature Communications.

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