Marquardt O, Bachmann P A
J Gen Virol. 1983 Jul;64 (Pt 7):1643-8. doi: 10.1099/0022-1317-64-7-1643.
A semi-quantitative analysis of hybrid formation between restriction enzyme-generated subgenomic fragments of cloned cDNA prepared from RNA of foot-and-mouth disease virus (FMDV) strain O1K and radiolabelled RNA from bovine enterovirus, bovine rhinovirus or Mengo virus indicated that the hybrids were of oligonucleotide size. They were located in those parts of the FMDV O1K genome that code for the two capsid proteins VP3 and VP1 and the precursor protein P52 as well as at the 3' end. No hybridization was observed with poliovirus type 1 RNA.
对从口蹄疫病毒(FMDV)O1K株RNA制备的克隆cDNA的限制性内切酶产生的亚基因组片段与来自牛肠道病毒、牛鼻病毒或门戈病毒的放射性标记RNA之间的杂交形成进行的半定量分析表明,杂交体为寡核苷酸大小。它们位于FMDV O1K基因组中编码两种衣壳蛋白VP3和VP1以及前体蛋白P52的部分以及3'末端。未观察到与1型脊髓灰质炎病毒RNA的杂交。