Literature DB >> 2018431

In vitro expression of a chimeric coat protein gene from Grapevine Fanleaf virus (strain F 13).

M A Serghini1, M Pinck, L Pinck.   

Abstract

The coat protein (CP) cistron of Grapevine Fanleaf virus strain F13 (GFLV-F13) has been located in the C-terminal region of the 122k polyprotein encoded by the genomic RNA 2 [Serghini et al. (1990) J. Gen. Virol. 71: 1433-1441]. A chimeric CP gene of GFLV-F13 including a short sequence corresponding to 3 restriction sites, the leader sequence of the GFLV-F13 satellite RNA and an initiation codon was constructed. Transcripts from this construct were translated in wheat germ extract with equal efficiency to form a 56k protein which comigrates on PAGE with the GFLV-F13 CP and a protein of 52k. Both species react with GFLV-F13 CP-specific antibodies. Deletions in the 5' region of the CP gene show that the 56k protein is initiated at the first AUG after the satellite leader and the 52k protein at the second in-frame AUG. Transcripts with a 142 nt deletion including the two AUG codons from the 5' end of the CP gene are not efficiently expressed in vitro, no major translation product being detected.

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Year:  1991        PMID: 2018431     DOI: 10.1007/bf01310773

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  18 in total

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Authors:  M Fuchs; M Pinck; M A Serghini; M Ravelonandro; B Walter; L Pinck
Journal:  J Gen Virol       Date:  1989-04       Impact factor: 3.891

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  3 in total

1.  Protection against virus infection in tobacco plants expressing the coat protein of grapevine fanleaf nepovirus.

Authors:  N Bardonnet; F Hans; M A Serghini; L Pinck
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Journal:  Plant Cell Rep       Date:  1995-06       Impact factor: 4.570

3.  Field safety assessment of recombination in transgenic grapevines expressing the coat protein gene of Grapevine fanleaf virus.

Authors:  Emmanuelle Vigne; Véronique Komar; Marc Fuchs
Journal:  Transgenic Res       Date:  2004-04       Impact factor: 3.145

  3 in total

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