Ishikawa M, Meshi T, Okada Y, Sano T, Shikata E
J Biochem. 1985 Dec;98(6):1615-20. doi: 10.1093/oxfordjournals.jbchem.a135431.
Previously we constructed an infectious hop stunt viroid (HSV) cDNA clone, PHS-P2P, which carries two copies of full-length HSV cDNA tandemly and generates HSV RNA when it is inoculated into cucumber plants. The in vitro transcript of the cDNA clone was also infectious. To investigate the essential regions for infectivity of HSV, we introduced a short deletion or insertion into the HSV sequence of pHS-P2P using restriction sites (XhoI site for pHI-X1, PvuI site for pHI-P1, and BamHI site for pHI-B1) and assayed the infectivities of these mutagenized clones. None of these mutagenized clones and their transcripts were infectious under the conditions used. Simultaneous inoculation of two or three of non-infectious mutagenized clones or the transcripts from them did not restore the infectivity.
此前我们构建了一个感染性啤酒花矮化类病毒(HSV)的cDNA克隆,即PHS-P2P,它串联携带两个全长HSV cDNA拷贝,并在接种到黄瓜植株中时产生HSV RNA。该cDNA克隆的体外转录本也具有感染性。为了研究HSV感染性的关键区域,我们利用限制性酶切位点(pHI-X1的XhoI位点、pHI-P1的PvuI位点和pHI-B1的BamHI位点)在pHS-P2P的HSV序列中引入了一个短缺失或插入,并检测了这些诱变克隆的感染性。在所用条件下,这些诱变克隆及其转录本均无感染性。同时接种两个或三个无感染性的诱变克隆或它们的转录本也不能恢复感染性。