We report the discovery of a novel archaeal AP endonuclease recovered from a metagenomic library constructed from environmental DNA collected in a salt marsh ecosystem. Using an ultra high throughput, cell free functional metagenomics workflow, we screened nuclease activities in an agnostic, single round selection format employing a DNA molecular beacon as the bait substrate. The recovered enzyme exhibits sequence and structural homology to human APE1 and displays overlapping substrate specific…

A prokaryotic RNA–directed targeting system can be designed to cleave any DNA sequence.

Endonuclease Enzymes Market To 2035: Gene Editing and Biopharma Demand Drive Expansion - News and Statistics  IndexBox

ALT: Chris Pratt as Andy Dwyer's Shocked Reaction

Closely related bacteriophages often display strikingly different infection phenotypes, yet the genetic basis of this variation remains poorly understood. Here, we uncover a previously unrecognized feature within the genus Teseptimavirus: the HNH endonuclease can occupy two distinct genomic positions, either associated with virion assembly or DNA packaging modules, suggesting functional specialization. We further demonstrate that this enzyme is closely linked to infection phenotypes, as even a single nucleotide substitution in the HNH gene significantly alters the efficiency of plating. These findings identify the HNH endonuclease as a key determinant of phage infectivity and reveal that its genomic context may shape functional outcomes. This work provides new insight into how subtle genetic differences drive phenotypic divergence among closely related phages and highlights the HNH endonuclease as a promising target for rational phage optimization in therapeutic and biocontrol applications.

To prevent future pandemics, it is important that we understand whether SARS-CoV-2 spilled over directly from animals to people, or indirectly in a laboratory accident. The genome of SARS-COV-2 contains a peculiar pattern of unique restriction endonuclease recognition sites allowing efficient dis- and re-assembly of the viral genome characteristic of synthetic viruses. Here, we report the likelihood of observing such a pattern in coronaviruses with no history of bioengineering. We find that SARS-CoV-2 is an anomaly, more likely a product of synthetic genome assembly than natural evolution. The restriction map of SARS-CoV-2 is consistent with many previously reported synthetic coronavirus genomes, meets all the criteria required for an efficient reverse genetic system, differs from closest relatives by a significantly higher rate of synonymous mutations in these synthetic-looking recognitions sites, and has a synthetic fingerprint unlikely to have evolved from its close relatives. We report a high likelihood that SARS-CoV-2 may have originated as an infectious clone assembled in vitro . Lay Summary To construct synthetic variants of natural coronaviruses in the lab, researchers often use a method called in vitro genome assembly. This method utilizes special enzymes called restriction enzymes to generate DNA building blocks that then can be “stitched” together in the correct order of the viral genome. To make a virus in the lab, researchers usually engineer the viral genome to add and remove stitching sites, called restriction sites. The ways researchers modify these sites can serve as fingerprints of in vitro genome assembly. We found that SARS-CoV has the restriction site fingerprint that is typical for synthetic viruses. The synthetic fingerprint of SARS-CoV-2 is anomalous in wild coronaviruses, and common in lab-assembled viruses. The type of mutations (synonymous or silent mutations) that differentiate the restriction sites in SARS-CoV-2 are characteristic of engineering, and the concentration of these silent mutations in the restriction sites is extremely unlikely to have arisen by random evolution. Both the restriction site fingerprint and the pattern of mutations generating them are extremely unlikely in wild coronaviruses and nearly universal in synthetic viruses. Our findings strongly suggest a synthetic origin of SARS-CoV2. ### Competing Interest Statement The authors declare no competing interests.

A clear understanding of the origin of SARS-CoV-2 is important for future pandemic preparedness. Here, I provided an updated analysis of the type IIS endonuclease maps in genomes of alphacoronavirus, ...

Oishi et al. successfully purified influenza PA-X to analyze its host shutoff mechanism using an endonuclease inhibitor. We found that PA-X binds RNA via its C-terminal domain to induce degradation, whereas vRNP assembly protects viral RNAs to selectively modulate the cellular environment.

Inteins are self-splicing proteins with a wide distribution in single-celled organisms, viruses, and plastids. The function of inteins remains an unanswered question. They may be regulatory elements as they must splice out of their host protein. However, recent research findings point to inteins likely being mobile selfish genetic elements capable of horizontal transfer. Here the intein inhabiting cyanobacterial DNA Polymerase III gamma/tau subunit (dnaX) serves as a case study into the conservation and phylogenetics of the intein compared to the host extein. Phylogenetic analysis reveals a sporadic distribution of intein alleles having an evolutionary history that is incongruent with the extein that may reticulate independently across clades. The dnaX intein can also contain an out-of-frame homing endonuclease (HE), a rarity for annotated inteins, that may have been the result of secondary invasion of an HE into a mini-intein. The simultaneous presence of intein-free and intein-containing alleles in populations of Microcystis aeruginosa challenges current theories about the life cycles of homing endonuclease containing selfish genetic elements and suggests that alternatives to the homing cycle need to be considered for intein persistence. Our analysis reveals an incongruent, disjointed distribution of this specific intein, suggesting that it is neither conserved among individual cyanobacterial lineages nor a critical component of dnaX functionality yet is able to persist in populations without being lost. ### Competing Interest Statement The authors have declared no competing interest.