Skip to main content

Zombies in our genes

Zombies in our genes helped us evolve, and could help battle cancers




Viruses are ubiquitous entities that have long plagued humans, often presenting in pesky, self-limiting infections, like a bout of the common cold. While most viral encounters are transient and merely inconvenient, some can have devastating or chronic consequences, leading to severe disease or even death. The recent COVID-19 pandemic and other emerging infectious diseases around us are good examples.

However, this battle between host and pathogen churns up a fascinating question: could viral infections have reshaped the human genome in the process?
Endogenous retroviruses (ERVs)
These remnants of ancient viral infections are embedded in the human genome and are often called "zombie" regions. ERVs were previously thought to be inactive, but recent studies suggest they can play a role in cancer. For example, the LTR10 retroelement in humans is thought to affect the formation of colorectal cancer tumors.

The LIF6 gene

This gene may have helped elephants evolve into their current size by suppressing or eliminating cancerous cells. It's thought that the TP53 gene and the LIF6 gene work together to stop cancer growth by suppressing damaged DNA.

Evolutionary tricks

Researchers can use evolutionary tricks to learn how defunct genes became functional again. For example, researchers can learn how the LIF6 gene was turned back on in elephants.

Here's some more information about ERVs and retroviruses:
Retroviruses are a group of viruses that can integrate and reshape the genomes of the hosts they infect.

ERVs are important for the existence of mammals because they helped the placenta evolve.

Cancer cells express many genes that shouldn't be on, and many of the switches that turn them on come from ancient viruses.

retroviruses, endogenous retroviruses, human evolution, ancient viruses, viral DNA, genetic material, immune system, cancer research, tumor suppression, gene regulation, antiviral defense, molecular biology, genome integration, epigenetics, cancer therapy, immunotherapy, genomic innovation, cellular mechanisms, human genome, evolutionary biology

#ZombiesInOurGenes, #HumanEvolution, #EndogenousRetroviruses, #AncientViruses, #GeneticInnovation, #ImmuneDefense, #CancerResearch, #TumorSuppression, #GeneRegulation, #AntiviralMechanisms, #Epigenetics, #ViralDNA, #GenomeIntegration, #CancerTherapy, #Immunotherapy, #MolecularBiology, #GenomicInnovation, #EvolutionaryBiology, #CellularMechanisms, #HumanGenome

Comments

Popular posts from this blog

Fruitful innovation

Fruitful innovation: Transforming watermelon genetics with advanced base editors The development of new adenine base editors (ABE) and adenine-to-thymine/ guanine base editors (AKBE) is transforming watermelon genetic engineering. These innovative tools enable precise A:T-to-G and A:T-to-T base substitutions, allowing for targeted genetic modifications. The research highlights the efficiency of these editors in generating specific mutations, such as a flowerless phenotype in ClFT (Y84H) mutant plants. This advancement not only enhances the understanding of gene function but also significantly improves molecular breeding, paving the way for more efficient watermelon crop improvement. Traditional breeding methods for watermelon often face challenges in achieving desired genetic traits efficiently and accurately. While CRISPR/Cas9 has provided a powerful tool for genome editing, its precision and scope are sometimes limited. These limitations highlight the need for more advanced gene-e...

Genetic factors with clinical trial stoppage

Genetic factors associated with reasons for clinical trial stoppage Many drug discovery projects are started but few progress fully through clinical trials to approval. Previous work has shown that human genetics support for the therapeutic hypothesis increases the chance of trial progression. Here, we applied natural language processing to classify the free-text reasons for 28,561 clinical trials that stopped before their endpoints were met. We then evaluated these classes in light of the underlying evidence for the therapeutic hypothesis and target properties. We found that trials are more likely to stop because of a lack of efficacy in the absence of strong genetic evidence from human populations or genetically modified animal models. Furthermore, certain trials are more likely to stop for safety reasons if the drug target gene is highly constrained in human populations and if the gene is broadly expressed across tissues. These results support the growing use of human genetics to ...

Genetics study on COVID-19

Large genetic study on severe COVID-19 Bonn researchers confirm three other genes for increased risk in addition to the known TLR7 gene Whether or not a person becomes seriously ill with COVID-19 depends, among other things, on genetic factors. With this in mind, researchers from the University Hospital Bonn (UKB) and the University of Bonn, in cooperation with other research teams from Germany, the Netherlands, Spain and Italy, investigated a particularly large group of affected individuals. They confirmed the central and already known role of the TLR7 gene in severe courses of the disease in men, but were also able to find evidence for a contribution of the gene in women. In addition, they were able to show that genetic changes in three other genes of the innate immune system contribute to severe COVID-19. The results have now been published in the journal " Human Genetics and Genomics Advances ". Even though the number of severe cases following infection with the SARS-CoV-...