Affiliation:
1. Department of Molecular Microbiology and Immunology, Life Sciences Center, University of Missouri—Columbia, School of Medicine, Columbia, Missouri
2. INRS—Institut Armand-Frappier, Université du Québec, Laval, Québec, Canada
Abstract
ABSTRACT
The RNA transcription profile of the goose parvovirus (GPV) was determined, and it is a surprising hybrid of features of the
Parvovirus
and
Dependovirus
genera of the
Parvovirinae
subfamily of the
Parvoviridae
. Similar to the
Dependovirus
adeno-associated virus type 5, RNAs transcribed from the GPV upstream P9 promoter, which encode the viral nonstructural proteins, were polyadenylated at a high efficiency at a polyadenylation site [(pA)p] located within an intron in the center of the genome. Efficient usage of (pA)p required a downstream element that overlaps with the polypyrimidine tract of the A2 3′ splice site of the central intron. An upstream element required for efficient use of (pA)p was also identified. RNAs transcribed from the P42 promoter, presumed to encode the viral capsid proteins, primarily extended through (pA)p and were polyadenylated at a site, (pA)d, located at the right end of the genome and ultimately spliced at a high efficiency. No promoter analogous to the
Dependovirus
P19 promoter was detected; however, similar to minute virus of mice and other members of the
Parvovirus
genus, a significant portion of pre-mRNAs generated from the P9 promoter were additionally spliced within the putative GPV Rep1 coding region and likely encode an additional, smaller, nonstructural protein. Also similar to members of the
Parvovirus
genus, detectable activity of the GPV P42 promoter was highly dependent on transactivation by the GPV Rep1 protein in a manner dependent on binding to a
cis
-element located in the P42 promoter.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
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