Milestone advance in silkworms could lead to commercial applications in medicine and textiles 

Once again, a scientific publication of one of our historic partners, EPFL – Brisken Lab, in the field of breast cancer. As stipulate in the article, there are few models to study some subtypes of breast cancer presenting a challenge for treatment. The collaboration between the Brisken Lab and GEG Tech work to design innovative models providing a useful tool for researchers performing preclinical studies and opening the way of new therapeutic approaches to address breast cancers.

About 6,000 newborns are diagnosed with Down syndrome each year in the United States. In most cases, these babies have a third copy of chromosome 21. An early mouse model, known as Ts65Dn, has been considered the standard for Down syndrome research, used in preclinical studies for nearly 30 years. Along with some successful cognitive treatments, such as a recent hormone-based cognitive treatment, some other treatments that were effective in the mouse model were not as effective in humans. It is important to note that the genome of the previous mouse model contains 45 additional genes that are not relevant to human Down syndrome. To create an improved mouse model of Down syndrome, researchers deleted these 45 additional genes using CRISPR gene editing technology. The researchers then compared the two mouse models and found that the 45 extra genes in the previous mouse model affect brain development and contributed to more severe motor, communication and memory difficulties. With this new and improved mouse model, the researchers hope to develop more specific treatments to improve cognition with the goal of developing independent living skills in people with Down syndrome.

Rat–human hybrid brains offer new ways to study human neurological disorders, but also raise ethical questions.

With over a hundred thousand people waiting for an organ transplant in the US alone, scientists are racing to find options besides human donors. Now for the first time, a pig kidney has been successfully transplanted into a person.

The combination of several genetic errors leads to the development of cancer and many other diseases based on genetic abnormalities. The 3Cs multiplex technique based on CRISPR-CAS technology developed at the Frankfurt Goethe University now offers the possibility to simulate combinations of millions of genetic defects and to study their effects in cell culture. Scientists at the Institute for Biochemistry II at Goethe University have enhanced the 3Cs technique which they developed and patented three years ago. 3Cs stands for covalent-closed circular-synthesized, because of the RNA parts used for CRISPR-CAS are produced with the help of a circular synthesis and are thus distributed more uniformly. With an entire library of such RNA rings, any gene in a cell can be specially addressed to change or cut it. The new 3Cs multiplex technique now even allows the simultaneous manipulation of two genes in one cell. This technique thus makes it possible to search very efficiently in cell culture experiments for genes that play a major role in cancer, and also in diseases of the nervous and immune systems, and that could be the potential target of certain treatments. certain treatments.

Pig-primate chimeras have been born live for the first time but died within a week. The two piglets, created by a team in China, looked normal although a small proportion of their cells were derived from cynomolgus monkeys.

“This is the first report of full-term pig-monkey chimeras,” says Tang Hai at the State Key Laboratory of Stem Cell and Reproductive Biology in Beijing.

Read more: https://link.springer.com/article/10.1007%2Fs13238-019-00676-8

Biologists have embraced CRISPR’s ability to quickly and cheaply modify the genomes of popular model organisms, such as mice, fruit flies and monkeys. Now they are trying the tool on more-exotic species, many of which have never been reared in a lab or had their genomes analysed. “We finally are ready to start expanding what we call a model organism,” says Tessa Montague, a molecular biologist at Columbia University in New York City. 

But the practical challenges of breeding and maintaining unconventional lab animals persist.

Researchers have developed a comprehensive way to evaluate how immune responses of humanized mice measure up to actual humans.

 Findings from the new study were published recently in Nature Communications through an article titled “Selective expansion of myeloid and NK cells in humanized mice yields human-like vaccine responses.”

On Wednesday, researchers from University of Texas Medical Branch published a new paper in the journal Science Translational Medicine.

In it, they detail their latest milestone along the path to creating lab-grown lungs for humans: they can now successfully transplant these bioengineered lungs into pigs.

Knock-in mice with precise insertions are efficiently generated through delivery of CRISPR–Cas9 to two-cell embryos.

Researchers from Columbia University found in 2017 that Crispr can cause genetic mutations and they have now been forced to accept their study was wrong and Crispr is harmless.

Ouistitis families are better suited to mimicking the genetically diverse human population than a colony of inbred rodents. To create marmosets with an inherited predisposition to Alzheimer's disease, researchers introduced a series of mutations in the PSEN1 gene using the Crispr/Cas9 genetic engineering system. These same mutations cause the early onset of Alzheimer's disease in humans. Presenilin-1, the protein encoded by PSEN1, plays a key role in the generation of amyloid tangles and, like human patients, marmosets carrying a mutation in the PSEN1 gene begin to develop Alzheimer's-type pathologies during adolescence. To characterize and validate the new model, the researchers are using a battery of non-invasive tests, including behavioral studies, longitudinal analysis of blood biomarkers and regular PET scans to assess brain function and pathological changes in brain tissue. The tests are designed to trace and compare the aging trajectory between healthy controls and animals genetically predisposed to the early onset of Alzheimer's disease, and to correlate progressive changes in the levels of amyloid and tau to changes in cognition. The researchers also plan to examine other factors that accompany disease progression, including epithelial permeability. 

Genomic studies of cancer patients have revealed thousands of mutations linked to tumor development. In an advance that could help scientists make a dent in that long list of unexplored mutations, MIT researchers designed their new mouse models by engineering the gene for the prime editor enzyme into the germline cells of the mice. The encoded prime editor enzyme allows cells to copy an RNA sequence into DNA that is incorporated into the genome. However, the prime editor gene remains silent until activated by the delivery of a specific protein called Cre recombinase. Since the prime editing system is installed in the mouse genome, researchers can initiate tumor growth by injecting Cre recombinase into the tissue where they want a cancer mutation to be expressed, along with a guide RNA that directs Cas9 nickase to make a specific edit in the cells' genome. The RNA guide can be designed to induce single DNA base substitutions, deletions, or additions in a specified gene, allowing the researchers to create any cancer mutation they wish. Using this technique, the researchers have created models of several different mutations of the cancer-causing gene Kras, in different organs. Such models could help researchers identify and test new drugs that target these mutations. 

Studies of diseases that affect the human brain are generally based on animal models that cannot replicate the complexity of human neuropathies. Consequently, these methodologies often fail when applied in a clinical setting with patients. In this context, the discoveries of cell reprogramming techniques to generate human neuron cultures from skin cells have revolutionized the study and development of innovative therapies in neuroscience. A study published in the journal Stem Cells Reports reveals that this cell reprogramming methodology allows the creation of neural networks that mimic unique features of human cells with temporal dynamics reminiscent of human brain development. Thus, cellular models based on reprogrammed human cells could stimulate the development of new effective therapies in the fight against neuropathies and, at the same time, reduce the use of experimental animals in the laboratory. In addition, cell reprogramming based on the induction of human pluripotent stem cells would allow the generation of patient-specific models and, using gene editing tools such as the CRISPR/Cas9 technique, it would be possible to obtain control cells in which the mutation responsible for the pathology is corrected. 

The genetically modified organs seemed to function for more than two days but some researchers are sceptical that the experiments had value.

Tumor suppressor genes block cell growth, preventing cancer cells from spreading. Scientists believe that mutations in these genes allow tumors to flourish unchecked. Now, Howard Hughes Medical Institute researcher Stephen Elledge's team has discovered a surprising new action for many of these faulty genes. Elledge had a hunch that defective tumor suppressor genes were doing something more than speeding up tumor cell growth. From a list of 7,500 genes, her team used CRISPR to engineer thousands of tumor cells. Each was missing a functional version of one of these genes. The researchers placed the cells in two types of mice: those with an immune system and those without. Then the team studied the tumors that developed. Elledge's method revealed the many different genes that tumors can mutate to evade the body's defenses. To explore the possible mechanisms triggered by the mutations, the researchers focused on a gene called GNA13. The gene's mutation protects cancer cells from the immune system's T cells, creating a safe space for the tumor to grow.

According to the study, more than 100 mutated tumor suppressor genes can prevent the immune system from identifying and destroying malignant cells in mice.

Swiss pharmaceutical company Novartis launched a lottery-style program to give away doses of its pricey gene therapy for free, drawing criticism from patient groups.

Australia has approved the use of CRISPR gene editing tool on plants and animals without the oversight of a governmental body. The controversial move has been called a 'middle ground' compared to regulations on other countries.

Police to investigate He Jiankui after last year’s claim to have altered the DNA of twin girls

For the first time, scientists have performed prenatal gene editing to prevent a lethal metabolic disorder in laboratory animals, offering the potential to treat human congenital diseases before birth. Published today in Nature Medicine, research from Children’s Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of Pennsylvania offers proof-of-concept for prenatal use of a sophisticated, low-toxicity tool that efficiently edits DNA building blocks in disease-causing genes.

OHSU scientists have discovered a naturally occurring disease in monkeys that mimics a deadly childhood neurodegenerative disorder in people – a finding that holds promise for developing new gene therapies to treat Batten disease.

Transplanting engineered neural cells into the brain of an amyotrophic lateral sclerosis (ALS) animal model delayed disease progression and extended the animals’ survival, a study shows.