Common origin of four diverse families of large eukaryotic DNA viruses

被引:445
作者
Iyer, LM [1 ]
Aravind, L [1 ]
Koonin, EV [1 ]
机构
[1] Natl Lib Med, Natl Ctr Biotechnol Informat, NIH, Bethesda, MD 20894 USA
关键词
D O I
10.1128/JVI.75.23.11720-11734.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Comparative analysis of the protein sequences encoded in the genomes of three families of large DNA viruses that replicate, completely or partly, in the cytoplasm of eukaryotic cells (poxviruses, asfarviruses, and iridoviruses) and phycodnaviruses that replicate in the nucleus reveals 9 genes that are shared by all of these viruses and 22 more genes that are present in at least three of the four compared viral families. Although orthologous proteins from different viral families typically show weak sequence similarity, because of which some of them have not been identified previously, at least five of the conserved genes appear to be synapomorphies (shared derived characters) that unite these four viral families, to the exclusion of all other known viruses and cellular life forms. Cladistic analysis with the genes shared by at least two viral families as evolutionary characters supports the monophyly of poxviruses, asfarviruses, iridoviruses, and phycodnaviruses. The results of genome comparison allow a tentative reconstruction of the ancestral viral genome and suggest that the common ancestor of all of these viral families was a nucleocytoplasmic virus with an icosahedral capsid, which encoded complex systems for DNA replication and transcription, a redox protein involved in disulfide bond formation in virion membrane proteins, and probably inhibitors of apoptosis. The conservation of the disulfide-oxidoreductase, a major capsid protein, and two virion membrane proteins indicates that the odd-shaped virions of poxviruses have evolved from the more common icosahedral virion seen in asfarviruses, iridoviruses, and phycodnaviruses.
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页码:11720 / 11734
页数:15
相关论文
共 76 条
[61]   Giant viruses infecting algae [J].
Van Etten, JL ;
Meints, RH .
ANNUAL REVIEW OF MICROBIOLOGY, 1999, 53 :447-494
[62]   A hypothesis for DNA viruses as the origin of eukaryotic replication proteins [J].
Villarreal, LP ;
DeFilippis, VR .
JOURNAL OF VIROLOGY, 2000, 74 (15) :7079-7084
[63]  
VINUELA E, 1985, CURR TOP MICROBIOL, V116, P151
[64]   THE ADENOVIRUS PROTEASE IS ACTIVATED BY A VIRUS-CODED DISULFIDE-LINKED PEPTIDE [J].
WEBSTER, A ;
HAY, RT ;
KEMP, G .
CELL, 1993, 72 (01) :97-104
[65]  
Whitley R, 1996, FIELDS VIROLOGY, P2297
[66]   The complete genome sequence of Shope (rabbit) fibroma virus [J].
Willer, DO ;
McFadden, G ;
Evans, DH .
VIROLOGY, 1999, 264 (02) :319-343
[67]   The iridoviruses [J].
Williams, T .
ADVANCES IN VIRUS RESEARCH, VOL 46, 1996, 46 :345-412
[68]   A MYRISTYLATED MEMBRANE-PROTEIN ENCODED BY THE VACCINIA VIRUS L1R OPEN READING FRAME IS THE TARGET OF POTENT NEUTRALIZING MONOCLONAL-ANTIBODIES [J].
WOLFFE, EJ ;
VIJAYA, S ;
MOSS, B .
VIROLOGY, 1995, 211 (01) :53-63
[69]   PURIFICATION OF THE LATE TRANSCRIPTION SYSTEM OF VACCINIA VIRUS - IDENTIFICATION OF A NOVEL TRANSCRIPTION FACTOR [J].
WRIGHT, CF ;
CORONEOS, AM .
JOURNAL OF VIROLOGY, 1993, 67 (12) :7264-7270
[70]   ORIGIN AND EVOLUTION OF RETROELEMENTS BASED UPON THEIR REVERSE-TRANSCRIPTASE SEQUENCES [J].
XIONG, Y ;
EICKBUSH, TH .
EMBO JOURNAL, 1990, 9 (10) :3353-3362