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FicD genes in invertebrates: A tale of transposons, pathogenic and integrated viruses.
Rosani, Umberto; De Felice, Sofia; Frizzo, Riccardo; Kawato, Satoshi; Wegner, K Mathias.
Afiliación
  • Rosani U; Department of Biology, University of Padova, 35121 Padova, Italy. Electronic address: umberto.rosani@unipd.it.
  • De Felice S; Department of Biology, University of Padova, 35121 Padova, Italy.
  • Frizzo R; Department of Biology, University of Padova, 35121 Padova, Italy.
  • Kawato S; Laboratory of Genome Science, Tokyo University of Marine Science and Technology, 108-8477 Tokyo, Japan.
  • Wegner KM; Alfred Wegener Institute - Helmholtz Centre for Polar and Marine Research, Waddensea Station Sylt, 25992 List, Germany.
Gene ; 893: 147895, 2024 Jan 30.
Article en En | MEDLINE | ID: mdl-37832807
ABSTRACT
Many gene families are shared across the tree of life between distantly related species because of horizontal gene transfers (HGTs). However, the frequency of HGTs varies strongly between gene families and biotic realms suggesting differential selection pressures and functional bias. One gene family with a wide distribution are FIC-domain containing enzymes (FicDs). FicDs catalyze AMPylation, a post-translational protein modification consisting in the addition of adenosine monophosphate to accessible residues of target proteins. Beside the well-known conservation of FicDs in deuterostomes, we report the presence of a conserved FicD gene ortholog in a large number of protostomes and microbial eukaryotes. We also reported additional FicD gene copies in the genomes of some rotifers, parasitic worms and bivalves. A few dsDNA viruses of these invertebrates, including White spot syndrome virus, Cherax quadricarinatus iridovirus, Ostreid herpesvirus-1 and the beetle nudivirus, carry copies of FicDs, with phylogenetic analysis suggesting a common origin of these FicD copies and the duplicated FicDs of their invertebrate hosts. HGTs and gene duplications possibly mediated by endogenous viruses or genetic mobile elements seem to have contributed to the transfer of AMPylation ability from bacteria and eukaryotes to pathogenic viruses, where this pathway could have been hijacked to promote viral infection.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Virosis / Invertebrados Límite: Animals Idioma: En Revista: Gene Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Virosis / Invertebrados Límite: Animals Idioma: En Revista: Gene Año: 2024 Tipo del documento: Article