Literature DB >> 7543587

Gene I mutants of peanut chlorotic streak virus, a caulimovirus, replicate in plants but do not move from cell to cell.

D A Ducasse1, A R Mushegian, R J Shepherd.   

Abstract

Gene I of peanut chlorotic streak virus (PCISV), a caulimovirus, is homologous to gene I of other caulimoviruses and may encode a protein for virus movement. To evaluate the function of gene I, several mutations were created in this gene of an infectious, partially redundant clone of PCISV. Constructs with an in-frame deletion and a single amino acid substitution in gene I were not infectious. To test for replication of these mutants in primarily infected cells, an immunosorbent PCR technique was devised. Virus particles formed by mutants in plants were recovered by binding to antivirus antibodies on a solid matrix and DNase treated to discriminate against residual inoculum, and DNA of trapped virions was subjected to PCR amplification. Gene I mutants were shown to direct formation of encapsidated DNA as revealed by a PCR product. Control gene V mutants (reverse transcriptase essential for replication) did not yield a PCR product. Quantitative PCR allowed estimation of the proportion of cells initially infected by gene I mutants and the amount of extractable virus per cell. It is concluded that PCISV gene I encodes a movement protein and that the immunoselection-PCR technique is useful in studying subliminal virus infection in plants.

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Year:  1995        PMID: 7543587      PMCID: PMC189441     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  25 in total

1.  Competitive PCR.

Authors:  P D Siebert; J W Larrick
Journal:  Nature       Date:  1992-10-08       Impact factor: 49.962

2.  The 30-kilodalton gene product of tobacco mosaic virus potentiates virus movement.

Authors:  C M Deom; M J Oliver; R N Beachy
Journal:  Science       Date:  1987-07-24       Impact factor: 47.728

3.  Cauliflower mosaic virus gene I product detected in a cell-wall-enriched fraction.

Authors:  H Albrecht; A Geldreich; J M de Murcia; D Kirchherr; J M Mesnard; G Lebeurier
Journal:  Virology       Date:  1988-04       Impact factor: 3.616

4.  Characteristics of the microplate method of enzyme-linked immunosorbent assay for the detection of plant viruses.

Authors:  M F Clark; A N Adams
Journal:  J Gen Virol       Date:  1977-03       Impact factor: 3.891

5.  Quantitative titration of nucleic acids by enzymatic amplification reactions run to saturation.

Authors:  C Pannetier; S Delassus; S Darche; C Saucier; P Kourilsky
Journal:  Nucleic Acids Res       Date:  1993-02-11       Impact factor: 16.971

6.  Absolute quantification of target DNA: a simple competitive PCR for efficient analysis of multiple samples.

Authors:  V Zachar; R A Thomas; A S Goustin
Journal:  Nucleic Acids Res       Date:  1993-04-25       Impact factor: 16.971

7.  Similarities between putative transport proteins of plant viruses.

Authors:  U Melcher
Journal:  J Gen Virol       Date:  1990-05       Impact factor: 3.891

8.  In vivo dimerization of cauliflower mosaic virus DNA can explain recombination.

Authors:  A Geldreich; G Lebeurier; L Hirth
Journal:  Gene       Date:  1986       Impact factor: 3.688

9.  Insertional mutagenesis of the cauliflower mosaic virus genome.

Authors:  S Daubert; R J Shepherd; R C Gardner
Journal:  Gene       Date:  1983-11       Impact factor: 3.688

Review 10.  Cell-to-cell movement of plant viruses. Insights from amino acid sequence comparisons of movement proteins and from analogies with cellular transport systems.

Authors:  A R Mushegian; E V Koonin
Journal:  Arch Virol       Date:  1993       Impact factor: 2.574

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