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The removal of one gene renders poxviruses—a lethal family of viral infections that are known to spread from animals to humans—harmless, a new study in the journal Science Advances reports.

During this ground-breaking study, scientists from the Spanish National Research Council and the University of Surrey investigated the immune response of cells to poxviruses. Poxviruses, such as cowpox and monkeypox, can spread to humans from infected animals, causing , fever, swollen lymph nodes and even death.

Viruses contain which helps them outsmart host cells, enabling replication and the spread of the . Cells in the body are comprised of molecules that sense the presence of viruses, sometimes via the recognition of their genetic material, and alert the immune system of an upcoming infection. Poxviruses, unlike other viruses, are highly unusual in that they have large DNA genomes that are replicated exclusively in the cell cytosol, an area of the cell full of sensors. How poxviruses manage to stay undetectable has remained unknown.

In the past decade, researchers have engineered an array of new tools that control the balance of genetic inheritance. Based on CRISPR technology, such gene drives are poised to move from the laboratory into the wild where they are being engineered to suppress devastating diseases such as mosquito-borne malaria, dengue, Zika, chikungunya, yellow fever and West Nile. Gene drives carry the power to immunize mosquitoes against malarial parasites, or act as genetic insecticides that reduce mosquito populations.

Although the newest gene drives have been proven to spread efficiently as designed in laboratory settings, concerns have been raised regarding the safety of releasing such systems into wild populations. Questions have emerged about the predictability and controllability of gene drives and whether, once let loose, they can be recalled in the field if they spread beyond their intended application region.

Now, scientists at the University of California San Diego and their colleagues have developed two new active genetic systems that address such risks by halting or eliminating gene drives in the wild. On Sept.18, 2020 in the journal Molecular Cell, research led by Xiang-Ru Xu, Emily Bulger and Valentino Gantz in the Division of Biological Sciences offers two new solutions based on elements developed in the common fruit fly.

Myotonic dystrophy type I is the most common type of adult-onset muscular dystrophy. People with the condition inherit repeated DNA segments that lead to the toxic buildup of repetitive RNA, the messenger that carries a gene’s recipe to the cell’s protein-making machinery. As a result, people born with myotonic dystrophy experience progressive muscle wasting and weakness and a wide variety of other debilitating symptoms.

CRISPR-Cas9 is a technique increasingly used in efforts to correct the genetic (DNA) defects that cause a variety of diseases. A few years ago, University of California San Diego School of Medicine researchers redirected the technique to instead modify RNA in a method they call RNA-targeting Cas9 (RCas9).

In a new study, publishing September 14, 2020 in Nature Biomedical Engineering, the team demonstrates that one dose of RCas9 gene therapy can chew up toxic RNA and almost completely reverse symptoms in a mouse model of myotonic dystrophy.

From the data, the GTEx team could identify the relationship between specific genes and a type of regulatory DNA called expression quantitative trait loci, or eQTL. At least one eQTL regulates almost every human gene, and each eQTL can regulate more than one gene, influencing expression, GTEx member and human geneticist Kristin Ardlie of the Broad Institute tells Science.

Another major takeaway from the analyses was that sex affected gene expression in almost all of the tissue types, from heart to lung to brain cells. “The vast majority of biology is shared by males and females,” yet the gene expression differences are vast and might explain differences in disease progression, GTEx study coauthor Barbara Stranger of Northwestern University’s Feinberg School of Medicine tells Science. “In the future, this knowledge may contribute to personalized medicine, where we consider biological sex as one of the relevant components of an individual’s characteristics,” she says in a statement issued by the Centre for Genome Regulation in Barcelona, where some of the researchers who participated in the GTEx project work.

Another of the studies bolsters the association between telomere length, ancestry, and aging. Telomere length is typically measured in blood cells; GTEx researchers examined it in 23 different tissue types and found blood is indeed a good proxy for overall length in other tissues. The team also showed that, as previously reported, shorter telomeres were associated with aging and longer ones were found in people of African ancestry. But not all earlier results held; the authors didn’t see a pattern of longer telomeres in females or constantly shorter telomeres across the tissues of smokers as previous studies had.

Not everyone is singing the project’s praises. Dan Graur, an evolutionary biologist at the University of Houston who often criticizes big projects like GTEx, tells Science the results are hard to parse and there was little diversity, with 85 percent of the tissue donors being white. He also was critical of the use of deceased donor tissue, questioning if it truly reflects gene activity in living humans. “It’s like studying the mating behaviour of roadkill.”

Other scientists say there’s much work to be done. The gene regulation map leaves many unanswered questions about the exact sequences that cause disease and how gene regulation systems work in tandem. Genomicist Ewan Birney, the deputy director general of EMBL, tells Science, “We shouldn’t pack up our bags and say gene expression is solved.”

Recently, San Diego Zoo partnered up with the wildlife preservation group Revive and Restore and a pet cloning company ViaGen Equine to create an exact copy of Kuporovic. The embryo was planted in a surrogate mother, a common horse.

Shawn Walker, the chief science officer at ViaGen Equine reports “This new Przewalski’s colt was born fully healthy and reproductively normal. He is head butting and kicking when his space is challenged, and he is demanding milk supply from his surrogate mother.”

This whole deal is not only good news for Przewalski’s horses, because this project demonstrates that we can keep genetic material viable for many years. Thus principles we see in action see here can potentially be applied to other endangered, even extinct species. Yes, you’ve read that right, Revive and Restore hopes to revive a wooly mammoth one day.

An endangered type of horse has successfully been cloned by scientists.

Kurt is a newborn Przewalski’s horse, a rare and endangered horse native.

He was born this year on August 6 after experts used genetic material that had been cryopreserved for 40 years.

Kurt’s birth is exciting not only because he’s very cute but because his genetic diversity could help to save the species.

A team of researchers from Stowers Institute for Medical Research, Howard Hughes Medical Institute and Stanford University has discovered conserved regeneration-responsive enhancers linked to tail regeneration in fish common to two species. In their paper published the journal Science, the group describes their genetic study of two fish species and what they learned about the role of conserved regeneration-responsive enhancers in allowing the fish to regenerate tail parts.

As the researchers note, some species are able to regenerate parts of their body when they are lost. For instance, lizards can regrow lost tails, while many other animals, including most mammals, cannot regrow damaged body parts. Despite much research, scientist have not been able to explain this. In this new effort, the researchers have found what they believe to be a major clue—conserved regeneration-responsive enhancers.

Prior research has shown that DNA sequences include non-coding bits called enhancers, which, as their name implies, play a role in enhancing gene activity. In this new effort, the researchers wondered if there might be certain enhancers involved in the regeneration response in fish—in this case, African killifish and zebrafish. They noted that prior research had shown that the two species split from the same genetic branch approximately 230 million years ago—a short enough period to allow them to see changes to their DNA that allowed both to regenerate the ends of their tails if they were bitten off by predators—or cut off by researchers.