Search bioRxiv⌕ Search

Biology subjects

de Oliveira Silva, Y. R.

Publications and source records attributed to de Oliveira Silva, Y. R..

2 recordsLinked to original sources

The bacterial antiphage protein Tiamat is an ATPase and DNase whose homologs are found across the tree of life

Bacteria and archaea encode hundreds of antiviral defense systems, some with homologs found in eukaryotic innate immunity. GHL ATPases like plant MORCs and prokaryotic Tiamat defend against viruses and phage, though their architecture and biochemical activities have remained unclear. Searching thousands of proteomes, we find Tiamat is rare in prokaryotes yet enriched across eukaryotes, including green plants, aquatic chordates, sponges, placozoans, and water molds. We resolve the central DUF3684 and flanking region into three predicted folds (TPR-like repeats, an uncharacterized conserved fold, and an inactive metalloprotease-like fold) that occupy the substrate-binding position of other GHL proteins. We show that purified Bacillus cereus Tiamat hydrolyzes ATP, inefficiently nicks duplex DNA, and cleaves single-stranded DNA site-specifically. We identify Tiamat-like proteins whose C-terminal nuclease is often swapped for helicases, peptidases, or other effectors. Additionally, we show Tiamat genes neighbor helicases, DNA methyltransferases, and nucleases, suggesting some Tiamats degrade foreign nucleic acid within a multi-component complex. Eukaryotic Tiamat homologs like the close Arabidopsis homolog NO VEIN and the distant human homolog SACSIN have acquired critical non-defense roles, leaving open whether these homologs remain antiviral or have been exapted.

biochemistry↗

Copper acquisition in Bacillus subtilis involves Cu(II) exchange between YcnI and YcnJ

The transition metal copper is biologically essential across all three domains of life. Several copper-dependent proteins and enzymes produced by the Gram-positive bacterium Bacillus subtilis have been characterized. However, many questions remain about how copper is recognized and trafficked to metalate cuproproteins. The ycnKJI operon in B. subtilis encodes a suite of proteins implicated in copper uptake and regulation, including the copper-binding protein YcnI and the putative copper importer YcnJ. Here, we demonstrate that one of the extracellular domains within YcnJ (YcnJCopC) binds Cu(II) in 1:1 stoichiometry with high affinity using a histidine brace motif. Biochemical results reveal that YcnJCopC and YcnI can exchange Cu(II). Genetic studies reveal that loss of either YcnI or YcnJ, or mutation of the key residues required for Cu(II)-binding, leads to a growth defect under conditions of copper limitation. Together, these data suggest that the Cu(II)-binding sites in both YcnI and YcnJ contribute to efficient import under Cu limited conditions. Our results support a model in which YcnI may sequester Cu(II) from YcnJ, serving a regulatory role to limit the amount of copper that enters the cytoplasm and allowing Cu(II) to be stored for later import in the outer face of the membrane. This transfer of Cu(II) between extracellular domains of membrane-bound proteins represents a potential new paradigm in bacterial copper usage.

biochemistry↗