Schneider P A, Kim R, Lipkin W I
Department of Microbiology and Molecular Genetics, University of California-Irvine, 92697-4290, USA.
J Virol. 1997 Jul;71(7):5614-9. doi: 10.1128/JVI.71.7.5614-5619.1997.
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 by leaky ribosomal scanning. Splicing of intron 1 enhances the translation of the G ORF by converting the M ORF into a 13-amino-acid minicistron, a structure that facilitates ribosomal reinitiation.
博尔纳病病毒反基因组包含五个主要开放阅读框(ORF),从5'到3'依次编码假定的核蛋白(N)、磷蛋白(P)、假定的基质蛋白(M)、主要糖蛋白(G)和RNA依赖的RNA聚合酶(pol)。N和P开放阅读框从单顺反子转录本翻译而来,而M、G和pol开放阅读框从多顺反子转录本翻译而来。M、G和pol开放阅读框的表达取决于两个内含子(内含子1,94个核苷酸[nt];内含子2,1294 nt)的差异剪接。野生型和突变序列的体外转录-翻译分析表明,G开放阅读框通过渗漏核糖体扫描从不剪接的2.8 kb RNA翻译而来。内含子1的剪接通过将M开放阅读框转化为一个13个氨基酸的小顺反子来增强G开放阅读框的翻译,这种结构有助于核糖体重新起始。