Giant viruses with an expanded complement of translation system components
Author(s) -
Frederik Schulz,
Natalya Yutin,
Natalia Ivanova,
Davi R. Ortega,
Tae Kwon Lee,
Julia Vierheilig,
Holger Daims,
Matthias Horn,
Michael Wagner,
Grant J. Jensen,
Nikos C. Kyrpides,
Eugene V. Koonin,
Tanja Woyke
Publication year - 2017
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aal4657
Subject(s) - translation (biology) , complement (music) , biology , virology , translation system , viral evolution , computational biology , genetics , rna , gene , messenger rna , phenotype , complementation , in vitro
The discovery of giant viruses blurred the sharp division between viruses and cellular life. Giant virus genomes encode proteins considered as signatures of cellular organisms, particularly translation system components, prompting hypotheses that these viruses derived from a fourth domain of cellular life. Here we report the discovery of a group of giant viruses (Klosneuviruses) in metagenomic data. Compared with other giant viruses, the Klosneuviruses encode an expanded translation machinery, including aminoacyl transfer RNA synthetases with specificities for all 20 amino acids. Notwithstanding the prevalence of translation system components, comprehensive phylogenomic analysis of these genes indicates that Klosneuviruses did not evolve from a cellular ancestor but rather are derived from a much smaller virus through extensive gain of host genes.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom