Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
1997-7-24
pubmed:databankReference
pubmed:abstractText
Analysis of the molluscum contagiosum virus (MCV) genome revealed that it encodes approximately 182 proteins, 105 of which have direct counterparts in orthopoxviruses (OPV). The corresponding OPV proteins comprise those known to be essential for replication as well as many that are still uncharacterized, including 2 of less than 60 amino acids that had not been previously noted. The OPV proteins most highly conserved in MCV are involved in transcription; the least conserved include membrane glycoproteins. Twenty of the MCV proteins with OPV counterparts also have cellular homologs and additional MCV proteins have conserved functional motifs. Of the 77 predicted MCV proteins without OPV counterparts, 10 have similarity to other MCV proteins and/or distant similarity to proteins of other poxviruses and 16 have cellular homologs including some predicted to antagonize host defenses. Clustering poxvirus proteins by sequence similarity revealed 3 unique MCV gene families and 8 families that are conserved in MCV and OPV. Two unique families contain putative membrane receptors; the third includes 2 proteins, each containing 2 DED apoptosis signal transduction domains. Additional families with conserved patterns of cysteines and putative redox active centers were identified. Promoters, transcription termination signals, and DNA concatemer resolution sequences are highly conserved in MCV and OPV. Phylogenetic analysis suggested that MCV, OPV, and leporipoxviruses radiated from a common poxvirus ancestor after the divergence of avipoxviruses. Despite the acquisition of unique genes for host interactions and changes in GC content, the physical order and regulation of essential ancestral poxvirus genes have been largely conserved in MCV and OPV.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0042-6822
pubmed:author
pubmed:issnType
Print
pubmed:day
23
pubmed:volume
233
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
19-42
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:9201214-Amino Acid Sequence, pubmed-meshheading:9201214-Animals, pubmed-meshheading:9201214-Apoptosis, pubmed-meshheading:9201214-Base Sequence, pubmed-meshheading:9201214-Cells, pubmed-meshheading:9201214-Consensus Sequence, pubmed-meshheading:9201214-Conserved Sequence, pubmed-meshheading:9201214-DNA, Viral, pubmed-meshheading:9201214-Genes, Viral, pubmed-meshheading:9201214-Genome, Viral, pubmed-meshheading:9201214-Humans, pubmed-meshheading:9201214-Inclusion Bodies, Viral, pubmed-meshheading:9201214-Molecular Sequence Data, pubmed-meshheading:9201214-Molluscum contagiosum virus, pubmed-meshheading:9201214-Open Reading Frames, pubmed-meshheading:9201214-Oxidation-Reduction, pubmed-meshheading:9201214-Phylogeny, pubmed-meshheading:9201214-Poxviridae, pubmed-meshheading:9201214-Promoter Regions, Genetic, pubmed-meshheading:9201214-Sequence Homology, Amino Acid, pubmed-meshheading:9201214-Transcription, Genetic, pubmed-meshheading:9201214-Viral Proteins
pubmed:year
1997
pubmed:articleTitle
The genome of molluscum contagiosum virus: analysis and comparison with other poxviruses.
pubmed:affiliation
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't