Cloning of the potato virus Y genes encoding the capsid protein CP and the nuclear inclusion protein NIb View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1989-03

AUTHORS

E. Wefels, H. Sommer, F. Salamini, W. Rohde

ABSTRACT

DNA was synthesized complementary to the RNA genome of potato virus Y (PVY; strain GO 16) and cloned into lambda vectors. The size of PVY-specific Eco RI-restricted cDNA ranged from 0.3 to approximately 22kb. Two of the cDNA clones each of which contained some 4kb of cDNA sequence starting from the 3'-polyadenylated terminus were characterized by sequence analysis. Presence of a single open reading frame suggests that PVY-specific proteins are synthesized as a polyprotein precursor. As with other sequenced potyvirus RNAs the gene for the PVY capsid protein CP is located next to the 3'-untranslated region followed by the genes for the putative RNA polymerase (nuclear inclusion protein NIb) and the virus-specific protease (nuclear inclusion protein NIa). The 3'-trailing sequence of the PVY strains cloned is highly homologous to the corresponding region of pepper mottle virus (PeMV) and suggests that PeMV is not a distinct member of the potyvirus group, but another strain of PVY. More... »

PAGES

123-134

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf01313884

DOI

http://dx.doi.org/10.1007/bf01313884

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1041442942

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/2802999


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