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      An insect picornavirus may have genome organization similar to that of caliciviruses

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          Abstract

          Computer‐assisted analysis of the amino acid sequence of the product encoded by the sequenced 3′ portion of the cricket paralysis virus (CrPV), an insect picornavirus, genome showed that this protein is homologous not to the RNA‐directed RNA polymerases, as originally suggested, but to the capsid proteins of mammalian picornaviruses. Alignment of the CrPV protein sequence with those of picornavirus and calicivirus capsid proteins demonstrated that the sequenced portion of the insect picornavirus genome encodes the C‐terminal part of VP3 and the entire VP1. Thus CrPV seems to have a genome organization distinct from that of other picornaviruses but closely resembling that of caliciviruses, with the capsid proteins encoded in the 3′ part of the genome. On the other hand, the tentative phylogenetic trees generated from the VP3 alignment revealed grouping of CrPV with hepatitis A virus, a true picornavirus, not with caliciviruses. Thus CrPV may be a picornavirus with a calicivirus‐like genome organization. Different options for CrPV genome expression are discussed.

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          Author and article information

          Journal
          FEBS Lett
          FEBS Lett
          10.1002/(ISSN)1873-3468
          FEB2
          Febs Letters
          John Wiley and Sons Inc. (Hoboken )
          0014-5793
          1873-3468
          03 February 1992
          16 January 2002
          : 297
          : 1-2 ( doiID: 10.1002/feb2.1992.297.issue-1-2 )
          : 81-86
          Affiliations
          [ 1 ]Institute of Microbiology, USSR Academy of Sciences, 117811 Moscow, USSR
          [ 2 ]Institute of Poliomyelitis and Viral Encephalitides, USSR Academy of Medical Sciences, 142782 Moscow Region, USSR
          Author notes
          [*]Correspondence address: E.V. Koonin, National Center for Biotechnology Information, National Library of Medicine, Bldg. 38A, N.I.H., 8600 Rockville Pike, Bethesda, MD 20894, USA.
          Article
          FEB2001457939280332B
          10.1016/0014-5793(92)80332-B
          7164100
          1551442
          1a62d860-d888-451e-9bcf-4d7b4b2efbf2
          FEBS Letters 297 (1992) 1873-3468 © 2015 Federation of European Biochemical Societies

          This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

          History
          : 29 November 1991
          Page count
          Pages: 6
          Categories
          Full‐length Article
          Full‐length Articles
          Custom metadata
          2.0
          February 03, 1992
          Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:15.04.2020

          Molecular biology
          picornavirus,calicivirus,capsid protein,rna-polymerase,viral genome organization,crpv,cricket paralysis virus,fmdvo1,foot-and-mouth disease virus, serotype o1,emcr,encephalomyocarditis virus, rueckert strain,mengo,mengo virus,tmebean,theiler murine encephalomyelitis virus, strain bean 8386,hav,hepatitis a virus, los angeles (chiron) strain,bev,bovine enterovirus,polioim,poliomyelitis virus, serotype 1, strain mahoney,rhino2,14 human rhinovirus, respective serotypes (all - picornaviruses),fecv,feline calicivirus,rhdv,rabbit hemorrhagic disease virus (both - caliciviruses)

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