Fédière G, El-Far M, Li Y, Bergoin M, Tijssen P
INRS-Institut Armand-Frappier, Université du Québec, Laval, Québec, Canada H7V 1B7.
Virology. 2004 Mar 1;320(1):181-9. doi: 10.1016/j.virol.2003.11.033.
The genome of Mythimna loreyi densovirus (MlDNV) was cloned into the pEMBL(19)+ vector. This clone was infectious upon transfection, both in LD cells and larvae. The genome possessed ITRs of 543 nucleotides of which the distal 126 nucleotides could form a hairpin. The nonstructural (NS) and structural (VP) genes were located on the 5'-halves of the complementary strands and their transcripts started 27 nts downstream of the ITRs. These transcripts had an overlap of 57 nucleotides in middle of the genome. The NS cassette consisted of three genes with NS1 and the overlapping NS2 downstream of NS3. The NS3 gene was spliced out from a fraction of the NS transcripts to allow leaky scanning translation of the downstream bicistronic NS1 and NS2 genes. The four VPs were similarly generated by leaky scanning translation of unspliced mRNA. The 5'-untranslated region of the VP transcript was only seven nucleotides long.
劳氏粘虫浓核病毒(MlDNV)的基因组被克隆到pEMBL(19)+载体中。该克隆在转染后具有感染性,无论是在LD细胞还是幼虫中。基因组拥有543个核苷酸的ITR,其中远端126个核苷酸可形成发夹结构。非结构(NS)基因和结构(VP)基因位于互补链的5'半段,其转录本起始于ITR下游27个核苷酸处。这些转录本在基因组中部有57个核苷酸的重叠。NS盒由三个基因组成,NS1以及位于NS3下游的重叠NS2。NS3基因从一部分NS转录本中剪接出来,以允许下游双顺反子NS1和NS2基因进行渗漏扫描翻译。四个VP同样通过未剪接mRNA的渗漏扫描翻译产生。VP转录本的5'非翻译区仅7个核苷酸长。