In the genome, olfactory endonuclease, as a special endonuclease, has the potential to change the rules of gene transmission. These endonucleases mainly exist in two forms: independent genes or fusions with host proteins. They are able to catalyze the hydrolysis of genomic DNA within the cells in which they are synthesized, but in most cases only act at a few locations. Due to this unique function, they play an important role in the gene delivery process, promoting horizontal transfer and promotion of genes.
This process, known as "homing," means that genes can spread through host populations at frequencies that exceed Mendelian rules, further changing the dynamics of evolution.
Although researchers are still exploring the specific origins and functions of olfactory endonucleases, there is a certain consensus that they are selfish genetic elements, similar to transposons. Not only do they promote their own reproduction, they do not need to provide a specific functional advantage to the host organism. The recognition sequences of these endonucleases are long, so their frequency of occurrence in the genome is very low, usually only once or a few times per genome.
The working mechanism of olfactory endonuclease is quite clever. When a genotype carries an allele (HEG+) that does not carry the endonuclease gene and an allele that does not carry it (HEG−), HEG− will be cleaved by the endonuclease, and then the host's DNA repair system will use the HEG+ DNA fragments of alleles are repaired. In this way, the endonuclease gene is copied into the allele that does not originally carry the gene.
All these processes demonstrate the "selfish" behavior of the olfactory endonuclease within the genome, promoting its own reproduction.
To facilitate classification, a specific nomenclature is implemented, usually with a prefix indicating their genomic origin, followed by a hyphen. For example, use "I-" as the prefix for those olfactory endonucleases encoded in introns, and "PI-" for those fused to host proteins. The name of each endonuclease also takes letters from the name of the organism from which they originate. This nomenclature is not only easy to remember, but also helps biologists accurately identify different endonucleases.
When we compare olfactory endonucleases to common restriction enzymes, we find that they differ in many ways. For example, restriction enzymes generally only recognize short, symmetrical sequences, whereas olfactory endonucleases specifically recognize longer, asymmetric sequences. This makes them very different in the adaptability of the target sequence and the degree of mutation allowed. In addition, olfactory endonucleases have a broader evolutionary distribution and are found in all biological kingdoms, including Archaea, Bacteria, and Eukaryotes.
These characteristics indicate that they may have evolved independently during the evolutionary process and formed unique biological functions.
Six structural types of olfactory endonucleases have been identified so far, and their conserved structural features allow scientists to better understand their functions in the genome. The most famous ones may include LAGLIDADG type and GIY-YIG type. These endonucleases cut and lock DNA through specific amino acid sequences, thereby protecting the transmission of their own genes.
For example, PI-Sce endonuclease is a LAGLIDADG-type endonuclease, which can self-cleave from a protein to become an independent functional protein and leave a deep imprint in the gene sequence.
With the deepening understanding of olfactory endonucleases, these "potential warriors of gene transmission" have undoubtedly changed the rules of the game for gene transmission and provided new perspectives and strategies for genomics research. In the future, these endonucleases may bring more possibilities to the development of genetic engineering and gene therapy. Are you also thinking about what profound impact these endonucleases will have on the evolution of organisms?