Evidence for translation of the Borna disease virus G protein by leaky ribosomal scanning and ribosomal reinitiation

被引:26
作者
Schneider, PA
Kim, R
Lipkin, WI
机构
[1] UNIV CALIF IRVINE,DEPT MICROBIOL & MOL GENET,LAB NEUROVIROL,IRVINE,CA 92697
[2] UNIV CALIF IRVINE,DEPT NEUROL,IRVINE,CA 92697
[3] UNIV CALIF IRVINE,DEPT ANAT & NEUROBIOL,IRVINE,CA 92697
关键词
D O I
10.1128/JVI.71.7.5614-5619.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Borna disease virus antigenome includes five major open reading frames (ORFs) which encode, from 5' to 3', the putative nucleoprotein (N), the phosphoprotein (P), the putative matrix protein (M), the major glycoprotein (G), and the RNA-dependent RNA polymerase (pol). Whereas the N and P ORFs are translated from monocistronic transcripts, the M, G, and pol ORFs are translated from polycistronic transcripts. Expression of the M, G, and pol ORFs is dependent upon differential splicing of two introns (intron 1, 94 nucleotides [nt]; intron 2, 1,294 nt). In vitro transcription-translation assays of wild-type and mutant sequences indicated that the G ORF is translated from an unspliced 2.8-kb RNA bg leaky ribosomal scanning, Splicing of intron 1 enhances the translation of the G ORF by converting the ill ORF into a 13-amino-acid minicistron, a structure that facilitates ribosomal reinitiation.
引用
收藏
页码:5614 / 5619
页数:6
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