D'Halluin J C, Cousin C, Boulanger P
J Virol. 1982 Feb;41(2):401-13. doi: 10.1128/JVI.41.2.401-413.1982.
The genome structures of about 100 interserotypic ts recombinants produced in crosses between human adenovirus type 2 (H2) and 5 (H5) temperature-sensitive mutants were analyzed by cleavage with restriction endonucleases to determine the map coordinates of the following temperature-sensitive mutants: penton base plus fiber-defective H2 ts103, -104, and -136, assembly-defective H2 ts112, fiber-defective H2 ts125, hexon-defective H2 ts118 and -121, and DNA-negative H2 ts111. H5 ts1 (100 K defective), H5 ts36 (DNA negative), H5 ts125 (mutated in the early 72,000-dalton protein), H5 ts22 (fiber defective), H5 ts58 (IIIa defective), and H5 ts18 and -19 were used as one of the parents. The physical locations of the H2 temperature-sensitive mutations thus defined are discussed in relation to the genetic map, the biological function altered, and the positions of the structural genes on the genome.
通过用限制性内切酶切割,分析了在人2型腺病毒(H2)和5型腺病毒(H5)温度敏感突变体杂交中产生的约100种血清型间ts重组体的基因组结构,以确定以下温度敏感突变体的图谱坐标:五邻体基座加纤维缺陷型H2 ts103、-104和-136,装配缺陷型H2 ts112,纤维缺陷型H2 ts125,六邻体缺陷型H2 ts118和-121,以及DNA阴性型H2 ts111。H5 ts1(100K缺陷型)、H5 ts36(DNA阴性型)、H5 ts125(在早期72000道尔顿蛋白中发生突变)、H5 ts22(纤维缺陷型)、H5 ts58(IIIa缺陷型)以及H5 ts18和-19用作亲本之一。本文结合遗传图谱、改变的生物学功能以及基因组上结构基因的位置,讨论了如此确定的H2温度敏感突变的物理位置。