Skip to main content

Heredity factors

Heredity factors is more than the sum of our genes



“Whereas genetics is the study of genes, epigenetics refers to a “layer” of additional information, which defines how these genes will or won’t be used by a cell. In other words, epigenetics refers to the study of changes in gene activity that do not change the DNA sequence and which can be conveyed during cell division.” Since the 1900s, studies have shown that epigenetic information can be passed on from one generation to the next, “but the molecular mechanisms had not been established“.

Nicola Iovino’s team at the Max Planck Institute for Immunobiology and Epigenetics in Freiburg, refers to the biological consequences of epigenetics for the first time in the Science journal. ” These studies not only show how epigenetic changes are transmitted from mother to offspring, but also the essential role played by these changes in embryo development. “

Gene expression changes throughout life, depending on the environment (pollution, for instance) and our lifestyle (diet, illness, stress, etc.). “Some so-called “epigenetic” information transmitted from parents to children, helps to regulate gene expression, which is inherited from one generation to the next.“

The study conducted by the German team not only demonstrates transformation for the next generation but also seems to be involved in embryo development per se. Scientists suppressed a gene with epigenetic changes in fruit fly embryos and, to their great surprise, “the embryos from which the gene was harvested, did not fully develop“. Thus “it seems that inherited epigenetic information is required to process and transcribe correctly the embryo genetic code,” explained Fides Zenk, co-author of the study.

The study concludes that environmental adaptations can be transmitted to offspring in some cases. This research also looks promising in terms of treatment for numerous diseases such as cancer since a disruption in epigenetic mechanisms could lead to the development of such conditions.

genetic inheritance, DNA, chromosomes, alleles, dominant traits, recessive traits, genotype, phenotype, autosomal inheritance, sex-linked traits, Mendelian genetics, mutations, genetic variation, hereditary disorders, gene expression, polygenic traits, pedigree analysis, genetic counseling, hereditary syndromes, familial traits

#Genetics, #Heredity, #DNA, #GeneticInheritance, #Genes, #MendelianGenetics, #GeneticDisorders, #TraitInheritance, #FamilyHistory, #Chromosomes, #Genotype, #Phenotype, #InheritedTraits, #Mutation, #GeneticCounseling, #RecessiveTraits, #DominantTraits, #GeneExpression, #PedigreeAnalysis, #HereditaryDiseases

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-...