Endoh H, Hirayama T, Aoyama T, Oka A
Laboratory of Molecular Biology, Kyoto University, Japan.
FEBS Lett. 1990 Oct 1;271(1-2):28-32. doi: 10.1016/0014-5793(90)80364-o.
We sequenced a 4.2-kb DNA region encompassing the vir A locus of the hairy-root-inducing plasmid pRiA4, and compared its sequence with the published vir A region sequences of four tumor-inducing plasmids. An open reading frame capable of coding for 829 amino acids was identified for vir A. Deletion mutants of vir A constructed by fusing to lacZ, but not the wild-type game itself, were efficiently expressed in Escherichia coli when they were put downstream front the lac promoter. These fused gene products became soluble or insoluble depending on the length of their lacZ moieties.
我们对包含发根诱导质粒pRiA4的vir A基因座的4.2 kb DNA区域进行了测序,并将其序列与已发表的四种肿瘤诱导质粒的vir A区域序列进行了比较。为vir A鉴定出一个能够编码829个氨基酸的开放阅读框。通过与lacZ融合构建的vir A缺失突变体,而非野生型基因本身,当置于lac启动子下游时能在大肠杆菌中高效表达。这些融合基因产物根据其lacZ部分的长度而变得可溶或不可溶。