Cited by 23Parvovirus B19 Infection StudiesAnimal Virus Infections StudiesVirus-based gene therapy research

The Complete Nucleotide Sequence of Parvovirus LuIII and Localization of a Unique Sequence Possibly Responsible for Its Encapsidation Pattern

Diffoot, Nanette, Chen, Katherine C., Bates, Robert C., Lederman, Muriel·1993·Virology

Abstract

Parvovirus LuIII encapsidates single-stranded DNA of either plus or minus polarity with equal frequency, whereas the rodent parvoviruses MVMp and H-1 encapsidate minus strand DNA only. A full-length, infectious clone of LuIII was constructed and the complete nucleotide sequence of the genome was determined. Comparison of the LuIII sequence with those of MVMp and H-1 revealed that these viruses are virtually identical with respect to the genomic organization, location of regulatory signals, mRNA splicing patterns, and amino acid sequences of viral proteins. However, two regions of the LuIII sequence differ significantly from those of the rodent parvoviruses. At mu 92, LuIII has only one copy of a sequence found as a direct repeat in MVMp and H-1. Upstream of this sequence, at mu 89, there is an A-T-rich region, 47 nucleotides in length, unique to the LuIII genome. This A-T-rich region could represent a signal responsible for the totally different encapsidation patterns observed for these viruses.

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Crossref · 10.1006/viro.1993.1040

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Authors
Diffoot, N., Chen, K. C., Bates, R. C., & Lederman, M.
Affiliations
Virginia Tech (US)
Venue
Virology
Publisher
Elsevier BV
Published
1993-01
Volume
192
Issue
1
Pages
339-345
ISSN
0042-6822 (ISSN-L)
OpenAlex
W2038021574
Cited by
23
References
0
Citations by year
2022: 1 · 2017: 1 · 2016: 1 · 2013: 1
FWCI
3.39
Type
journal article
Language
en
Open access
closed
Locations
  • Virology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Infectious Diseases › Parvovirus B19 Infection Studies
  • Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Virus Infections Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Virus-based gene therapy research
Keywords
viral encapsidation, A+T-rich region, direct repeats, parvovirus H-1, viral genome structure, mRNA splicing, infectious clone
MeSH terms
Base Sequence, Capsid, Cloning, Molecular, DNA, Viral, Genes, Viral, Molecular Sequence Data, Parvoviridae, Viral Structural Proteins, Open Reading Frames, Sequence Alignment, Viral Nonstructural Proteins, Sequence Homology, Amino Acid

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